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<title>Nature Reviews Urology</title>
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                     <title>Prostate cancer: The future of TRUS-guided biopsy antibiotic prophylaxis?</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/6kRFeudY02o/nrurol.2012.69</link>
<description>Transrectal ultrasonography (TRUS)-guided biopsy is the recommended tool for the diagnosis of prostate cancer. However, it is associated with a risk of sepsis caused by the transfer of bowel flora into the bloodstream during the biopsy procedure, as well as other complications including hematuria, hematospermia, </description>
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<p>
<b>Prostate cancer: The future of TRUS-guided biopsy antibiotic prophylaxis?</b>
</p>
<p>Nature Reviews Urology 9, 233 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.69">doi:10.1038/nrurol.2012.69</a>
</p>
<p>Author: Annette Fenner</p>
<p>Transrectal ultrasonography (TRUS)-guided biopsy is the recommended tool for the diagnosis of prostate cancer. However, it is associated with a risk of sepsis caused by the transfer of bowel flora into the bloodstream during the biopsy procedure, as well as other complications including hematuria, hematospermia, </p>
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<dc:title>Prostate cancer: The future of TRUS-guided biopsy antibiotic prophylaxis?</dc:title>
<dc:creator>Annette Fenner</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.69</dc:identifier>
<dc:source>Nature Reviews Urology 9, 233 (2012)</dc:source>
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                     <title>Bladder cancer: New insight into the mechanisms of lung metastasis</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/1ksVv3O2hl4/nrurol.2012.60</link>
<description>Metastatic bladder cancer is associated with a very poor prognosis—the survival rate at 5 years is less than 10%. New research into how bladder cancer spreads to the lung, reported by Dan Theodorescu and colleagues in the Journal of Clinical Investigation, might pave the </description>
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<p>
<b>Bladder cancer: New insight into the mechanisms of lung metastasis</b>
</p>
<p>Nature Reviews Urology 9, 234 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.60">doi:10.1038/nrurol.2012.60</a>
</p>
<p>Author: Sarah Payton</p>
<p>Metastatic bladder cancer is associated with a very poor prognosis&#8212;the survival rate at 5 years is less than 10%. New research into how bladder cancer spreads to the lung, reported by Dan Theodorescu and colleagues in the Journal of Clinical Investigation, might pave the </p>
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<dc:title>Bladder cancer: New insight into the mechanisms of lung metastasis</dc:title>
<dc:creator>Sarah Payton</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.60</dc:identifier>
<dc:source>Nature Reviews Urology 9, 234 (2012)</dc:source>
<dc:date>2012-04-17</dc:date>
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                     <title>Prostate cancer: 11 years follow-up for ERSPC</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/fJVFgtvbIxM/nrurol.2012.66</link>
<description>Studies investigating the effect of PSA screening on prostate cancer mortality have produced conflicting results and the use of PSA as a screening tool remains controversial. Many clinicians continue to express concern over the effects of overdiagnosing incidental and clinically insignificant cancers, which do not </description>
<content:encoded><![CDATA[

<p>
<b>Prostate cancer: 11 years follow-up for ERSPC</b>
</p>
<p>Nature Reviews Urology 9, 234 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.66">doi:10.1038/nrurol.2012.66</a>
</p>
<p>Author: Annette Fenner</p>
<p>Studies investigating the effect of PSA screening on prostate cancer mortality have produced conflicting results and the use of PSA as a screening tool remains controversial. Many clinicians continue to express concern over the effects of overdiagnosing incidental and clinically insignificant cancers, which do not </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/fJVFgtvbIxM" height="1" width="1"/>]]></content:encoded>
<dc:title>Prostate cancer: 11 years follow-up for ERSPC</dc:title>
<dc:creator>Annette Fenner</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.66</dc:identifier>
<dc:source>Nature Reviews Urology 9, 234 (2012)</dc:source>
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                     <title>BPH: Hormone antagonists for two-pronged attack on BPH</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/ZL40Hn9rb7E/nrurol.2012.67</link>
<description>New data published in the Journal of Urology have shown a positive effect of combined therapy with antagonists of growth hormone-releasing hormone (GHRH) and luteinizing hormone-releasing hormone (LHRH) on rat models of BPH.Following on from previous research that identified potential roles for GHRH </description>
<content:encoded><![CDATA[

<p>
<b>BPH: Hormone antagonists for two-pronged attack on BPH</b>
</p>
<p>Nature Reviews Urology 9, 235 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.67">doi:10.1038/nrurol.2012.67</a>
</p>
<p>Author: Melanie Clyne</p>
<p>New data published in the Journal of Urology have shown a positive effect of combined therapy with antagonists of growth hormone-releasing hormone (GHRH) and luteinizing hormone-releasing hormone (LHRH) on rat models of BPH.Following on from previous research that identified potential roles for GHRH </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/ZL40Hn9rb7E" height="1" width="1"/>]]></content:encoded>
<dc:title>BPH: Hormone antagonists for two-pronged attack on BPH</dc:title>
<dc:creator>Melanie Clyne</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.67</dc:identifier>
<dc:source>Nature Reviews Urology 9, 235 (2012)</dc:source>
<dc:date>2012-04-17</dc:date>
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                     <title>Prostate cancer: New light shed on the anticancer effects of zoledronic acid</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/VVg-Ey0THDU/nrurol.2012.70</link>
<description>According to new research published in Prostate Cancer and Prostatic Diseases, zoledronic acid—an osteoclast-targeting bisphosphonate that prevents loss of bone mass—directly inhibits prostate cancer proliferation and motility, without disrupting interactions between the tumor and the vascular wall.Previous preclinical studies have reported anticancer activities </description>
<content:encoded><![CDATA[

<p>
<b>Prostate cancer: New light shed on the anticancer effects of zoledronic acid</b>
</p>
<p>Nature Reviews Urology 9, 235 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.70">doi:10.1038/nrurol.2012.70</a>
</p>
<p>Author: Melanie Clyne</p>
<p>According to new research published in Prostate Cancer and Prostatic Diseases, zoledronic acid&#8212;an osteoclast-targeting bisphosphonate that prevents loss of bone mass&#8212;directly inhibits prostate cancer proliferation and motility, without disrupting interactions between the tumor and the vascular wall.Previous preclinical studies have reported anticancer activities </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/VVg-Ey0THDU" height="1" width="1"/>]]></content:encoded>
<dc:title>Prostate cancer: New light shed on the anticancer effects of zoledronic acid</dc:title>
<dc:creator>Melanie Clyne</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.70</dc:identifier>
<dc:source>Nature Reviews Urology 9, 235 (2012)</dc:source>
<dc:date>2012-04-24</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
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                     <title>Prostate cancer: Circumcision associated with reduced risk</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/eFSRQeqBoOY/nrurol.2012.62</link>
<description>A case-control study has found that men who are circumcised before their first sexual intercourse are 15% less likely to develop prostate cancer than men who are not or who were circumcised after first intercourse (95% CI, 0.73–0.99). The data was collected from 1,754 men </description>
<content:encoded><![CDATA[

<p>
<b>Prostate cancer: Circumcision associated with reduced risk</b>
</p>
<p>Nature Reviews Urology 9, 236 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.62">doi:10.1038/nrurol.2012.62</a>
</p>
<p>A case-control study has found that men who are circumcised before their first sexual intercourse are 15% less likely to develop prostate cancer than men who are not or who were circumcised after first intercourse (95% CI, 0.73&#8211;0.99). The data was collected from 1,754 men </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/eFSRQeqBoOY" height="1" width="1"/>]]></content:encoded>
<dc:title>Prostate cancer: Circumcision associated with reduced risk</dc:title>
<dc:identifier>doi:10.1038/nrurol.2012.62</dc:identifier>
<dc:source>Nature Reviews Urology 9, 236 (2012)</dc:source>
<dc:date>2012-04-03</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-03</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.62</prism:doi>
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<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>236</prism:startingPage>
<prism:endingPage>236</prism:endingPage>
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                     <title>Infection: Delayed-release doxycycline might improve compliance</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/6BmTsIzK5ew/nrurol.2012.63</link>
<description>A multicenter phase III clinical trial of more than 400 patients has found that once-daily 200 mg delayed-release doxycycline (WC2031) is noninferior to twice-daily 100 mg doxycycline (Vibramycin) in treating uncomplicated urogenital chlamydia. Furthermore, WC2031 was better tolerated and demonstrated a similar safety profile to </description>
<content:encoded><![CDATA[

<p>
<b>Infection: Delayed-release doxycycline might improve compliance</b>
</p>
<p>Nature Reviews Urology 9, 236 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.63">doi:10.1038/nrurol.2012.63</a>
</p>
<p>A multicenter phase III clinical trial of more than 400 patients has found that once-daily 200 mg delayed-release doxycycline (WC2031) is noninferior to twice-daily 100 mg doxycycline (Vibramycin) in treating uncomplicated urogenital chlamydia. Furthermore, WC2031 was better tolerated and demonstrated a similar safety profile to </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/6BmTsIzK5ew" height="1" width="1"/>]]></content:encoded>
<dc:title>Infection: Delayed-release doxycycline might improve compliance</dc:title>
<dc:identifier>doi:10.1038/nrurol.2012.63</dc:identifier>
<dc:source>Nature Reviews Urology 9, 236 (2012)</dc:source>
<dc:date>2012-04-03</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-03</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.63</prism:doi>
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<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>236</prism:startingPage>
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                     <title>Sexual dysfunction: Mulberry extract improves erectile function in diabetic mice</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/szlqrdNQwKM/nrurol.2012.64</link>
<description>Treatment of diabetic mice with cyanidin-3-O-β-D-glucopyranoside extracted from mulberry fruit improves erectile function compared with diabetic mice that did not receive the treatment. The corporal tissues of the treated mice showed increased expression of nitric oxide synthase (NOS) and </description>
<content:encoded><![CDATA[

<p>
<b>Sexual dysfunction: Mulberry extract improves erectile function in diabetic mice</b>
</p>
<p>Nature Reviews Urology 9, 236 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.64">doi:10.1038/nrurol.2012.64</a>
</p>
<p>Treatment of diabetic mice with cyanidin-3-O-&#946;-D-glucopyranoside extracted from mulberry fruit improves erectile function compared with diabetic mice that did not receive the treatment. The corporal tissues of the treated mice showed increased expression of nitric oxide synthase (NOS) and </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/szlqrdNQwKM" height="1" width="1"/>]]></content:encoded>
<dc:title>Sexual dysfunction: Mulberry extract improves erectile function in diabetic mice</dc:title>
<dc:identifier>doi:10.1038/nrurol.2012.64</dc:identifier>
<dc:source>Nature Reviews Urology 9, 236 (2012)</dc:source>
<dc:date>2012-04-03</dc:date>
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                     <title>Kidney cancer: αB-Crystallin expression is increased in ccRCC</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/TojKCfqnJok/nrurol.2012.65</link>
<description>Clear-cell renal cell carcinomas (ccRCCs) overexpress the heat shock protein αB-crystallin, which might enhance cell growth and migration, according to a new study that analyzed 50 ccRCC tissue samples. αB-Crystallin expression was also correlated with overall survival of patients with ccRCC. Interestingly, overexpression of αB-crystallin </description>
<content:encoded><![CDATA[

<p>
<b>Kidney cancer: &#945;B-Crystallin expression is increased in ccRCC</b>
</p>
<p>Nature Reviews Urology 9, 236 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.65">doi:10.1038/nrurol.2012.65</a>
</p>
<p>Clear-cell renal cell carcinomas (ccRCCs) overexpress the heat shock protein &#945;B-crystallin, which might enhance cell growth and migration, according to a new study that analyzed 50 ccRCC tissue samples. &#945;B-Crystallin expression was also correlated with overall survival of patients with ccRCC. Interestingly, overexpression of &#945;B-crystallin </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/TojKCfqnJok" height="1" width="1"/>]]></content:encoded>
<dc:title>Kidney cancer: αB-Crystallin expression is increased in ccRCC</dc:title>
<dc:identifier>doi:10.1038/nrurol.2012.65</dc:identifier>
<dc:source>Nature Reviews Urology 9, 236 (2012)</dc:source>
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<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-03</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.65</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.65</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>236</prism:startingPage>
<prism:endingPage>236</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.65</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.80">
                     <title>Prostate cancer: One step closer to personalized therapy with cell capturing</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/n4ODecP7Ybc/nrurol.2012.80</link>
<description>A major challenge in treating metastatic prostate cancer is that secondary tumors, and the circulating cells that seed them, are fundamentally different to the primary lesion from which they are thought to originate. In the current era of intense research into personalized therapy, understanding the </description>
<content:encoded><![CDATA[

<p>
<b>Prostate cancer: One step closer to personalized therapy with cell capturing</b>
</p>
<p>Nature Reviews Urology 9, 236 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.80">doi:10.1038/nrurol.2012.80</a>
</p>
<p>Author: Mina Razzak</p>
<p>A major challenge in treating metastatic prostate cancer is that secondary tumors, and the circulating cells that seed them, are fundamentally different to the primary lesion from which they are thought to originate. In the current era of intense research into personalized therapy, understanding the </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/n4ODecP7Ybc" height="1" width="1"/>]]></content:encoded>
<dc:title>Prostate cancer: One step closer to personalized therapy with cell capturing</dc:title>
<dc:creator>Mina Razzak</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.80</dc:identifier>
<dc:source>Nature Reviews Urology 9, 236 (2012)</dc:source>
<dc:date>2012-04-24</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-24</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.80</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.80</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>236</prism:startingPage>
<prism:endingPage>236</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.80</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.71">
                     <title>Prostate cancer: Smoothened inhibition reduces tumor cell proliferation</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/VNnkd9uMafw/nrurol.2012.71</link>
<description>New research published in The Prostate supports the hypothesis that increased Hedgehog ligands produced by epithelial cancer cells activate the Hedgehog pathway in the adjacent stromal microenvironment, which in turn enhances tumor survival and proliferation. Inhibition of the Hedgehog signaling pathway using the small </description>
<content:encoded><![CDATA[

<p>
<b>Prostate cancer: Smoothened inhibition reduces tumor cell proliferation</b>
</p>
<p>Nature Reviews Urology 9, 237 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.71">doi:10.1038/nrurol.2012.71</a>
</p>
<p>Author: Mina Razzak</p>
<p>New research published in The Prostate supports the hypothesis that increased Hedgehog ligands produced by epithelial cancer cells activate the Hedgehog pathway in the adjacent stromal microenvironment, which in turn enhances tumor survival and proliferation. Inhibition of the Hedgehog signaling pathway using the small </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/VNnkd9uMafw" height="1" width="1"/>]]></content:encoded>
<dc:title>Prostate cancer: Smoothened inhibition reduces tumor cell proliferation</dc:title>
<dc:creator>Mina Razzak</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.71</dc:identifier>
<dc:source>Nature Reviews Urology 9, 237 (2012)</dc:source>
<dc:date>2012-04-17</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-17</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.71</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.71</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>237</prism:startingPage>
<prism:endingPage>237</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.71</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.82">
                     <title>Prostate cancer: Hypoxia predicts relapse and recurrence after radiotherapy</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/0TRwLnkf7Q4/nrurol.2012.82</link>
<description>Tumor hypoxia is associated with early biochemical relapse after radiotherapy for prostate cancer and with local recurrence, according to a new study from a team in Toronto, Canada.Studies have suggested that hypoxia modulates tumor behavior and treatment response, promoting both aggressiveness and metastasis. “Many </description>
<content:encoded><![CDATA[

<p>
<b>Prostate cancer: Hypoxia predicts relapse and recurrence after radiotherapy</b>
</p>
<p>Nature Reviews Urology 9, 237 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.82">doi:10.1038/nrurol.2012.82</a>
</p>
<p>Author: Annette Fenner</p>
<p>Tumor hypoxia is associated with early biochemical relapse after radiotherapy for prostate cancer and with local recurrence, according to a new study from a team in Toronto, Canada.Studies have suggested that hypoxia modulates tumor behavior and treatment response, promoting both aggressiveness and metastasis. &#8220;Many </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/0TRwLnkf7Q4" height="1" width="1"/>]]></content:encoded>
<dc:title>Prostate cancer: Hypoxia predicts relapse and recurrence after radiotherapy</dc:title>
<dc:creator>Annette Fenner</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.82</dc:identifier>
<dc:source>Nature Reviews Urology 9, 237 (2012)</dc:source>
<dc:date>2012-04-24</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-24</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.82</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.82</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>237</prism:startingPage>
<prism:endingPage>237</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.82</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.72">
                     <title>Prostate cancer: Does the distribution of proerectile nerves support the use of a high anterior incision?</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/C8pVZLEjstA/nrurol.2012.72</link>
<description>A team of researchers from Germany, led by Roman Ganzer, has examined the topographical distribution of nerves around the prostate in order to clarify which regions are important for erectile function. “Our intention was to use immunohistochemistry to distinguish proerectile parasympathetic nerves from nonerectile sympathetic </description>
<content:encoded><![CDATA[

<p>
<b>Prostate cancer: Does the distribution of proerectile nerves support the use of a high anterior incision?</b>
</p>
<p>Nature Reviews Urology 9, 238 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.72">doi:10.1038/nrurol.2012.72</a>
</p>
<p>Author: Sarah Payton</p>
<p>A team of researchers from Germany, led by Roman Ganzer, has examined the topographical distribution of nerves around the prostate in order to clarify which regions are important for erectile function. &#8220;Our intention was to use immunohistochemistry to distinguish proerectile parasympathetic nerves from nonerectile sympathetic </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/C8pVZLEjstA" height="1" width="1"/>]]></content:encoded>
<dc:title>Prostate cancer: Does the distribution of proerectile nerves support the use of a high anterior incision?</dc:title>
<dc:creator>Sarah Payton</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.72</dc:identifier>
<dc:source>Nature Reviews Urology 9, 238 (2012)</dc:source>
<dc:date>2012-04-24</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-24</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.72</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.72</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>238</prism:startingPage>
<prism:endingPage>238</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.72</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.83">
                     <title>Sexual dysfunction: Psychological inputs to sexual dysfunction</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/Y3QLUMVRoDg/nrurol.2012.83</link>
<description>New data published in the Journal of Sexual Medicine has provided supportive evidence for associations between sexual dysfunction and psychological conditions such as anxiety and depression. In one study, Burri  et al. studied 930 female twins and established a strong association between </description>
<content:encoded><![CDATA[

<p>
<b>Sexual dysfunction: Psychological inputs to sexual dysfunction</b>
</p>
<p>Nature Reviews Urology 9, 238 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.83">doi:10.1038/nrurol.2012.83</a>
</p>
<p>Author: Melanie Clyne</p>
<p>New data published in the Journal of Sexual Medicine has provided supportive evidence for associations between sexual dysfunction and psychological conditions such as anxiety and depression. In one study, Burri  et al. studied 930 female twins and established a strong association between </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/Y3QLUMVRoDg" height="1" width="1"/>]]></content:encoded>
<dc:title>Sexual dysfunction: Psychological inputs to sexual dysfunction</dc:title>
<dc:creator>Melanie Clyne</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.83</dc:identifier>
<dc:source>Nature Reviews Urology 9, 238 (2012)</dc:source>
<dc:date>2012-04-24</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-24</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.83</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.83</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>238</prism:startingPage>
<prism:endingPage>238</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.83</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.81">
                     <title>Prostatitis: Insights into chronic pelvic pain</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/MJfyKODEZRM/nrurol.2012.81</link>
<description>Two studies in the Scandinavian Journal of Urology and Nephrology have sought to improve our understanding of chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS).CP/CPPS is often associated with a severe reduction in quality of life, with patients reporting persistent and relapsing pain, irritative urinary </description>
<content:encoded><![CDATA[

<p>
<b>Prostatitis: Insights into chronic pelvic pain</b>
</p>
<p>Nature Reviews Urology 9, 239 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.81">doi:10.1038/nrurol.2012.81</a>
</p>
<p>Author: Annette Fenner</p>
<p>Two studies in the Scandinavian Journal of Urology and Nephrology have sought to improve our understanding of chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS).CP/CPPS is often associated with a severe reduction in quality of life, with patients reporting persistent and relapsing pain, irritative urinary </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/MJfyKODEZRM" height="1" width="1"/>]]></content:encoded>
<dc:title>Prostatitis: Insights into chronic pelvic pain</dc:title>
<dc:creator>Annette Fenner</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.81</dc:identifier>
<dc:source>Nature Reviews Urology 9, 239 (2012)</dc:source>
<dc:date>2012-04-24</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-24</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.81</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.81</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>239</prism:startingPage>
<prism:endingPage>239</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.81</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.73">
                     <title>Sexual dysfunction: Ergot alkaloids influence erectile function</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/pHEngGneXvA/nrurol.2012.73</link>
<description>The ergot alkaloids dihydroergotoxine and bromocriptine are erectogenic agents, according to a new preclinical study in rats. By contrast, the alkaloid ergotamine demonstrated detumescent properties in these animals. When injected intrapenially, dihydroergotoxine (at doses of 0.1–1.0 mg/0.1 ml) induced longer erections than a saline solution </description>
<content:encoded><![CDATA[

<p>
<b>Sexual dysfunction: Ergot alkaloids influence erectile function</b>
</p>
<p>Nature Reviews Urology 9, 240 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.73">doi:10.1038/nrurol.2012.73</a>
</p>
<p>The ergot alkaloids dihydroergotoxine and bromocriptine are erectogenic agents, according to a new preclinical study in rats. By contrast, the alkaloid ergotamine demonstrated detumescent properties in these animals. When injected intrapenially, dihydroergotoxine (at doses of 0.1&#8211;1.0 mg/0.1 ml) induced longer erections than a saline solution </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/pHEngGneXvA" height="1" width="1"/>]]></content:encoded>
<dc:title>Sexual dysfunction: Ergot alkaloids influence erectile function</dc:title>
<dc:identifier>doi:10.1038/nrurol.2012.73</dc:identifier>
<dc:source>Nature Reviews Urology 9, 240 (2012)</dc:source>
<dc:date>2012-04-17</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-17</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.73</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.73</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>240</prism:startingPage>
<prism:endingPage>240</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.73</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.74">
                     <title>Sexual dysfunction: Avanafil is a safe and efficacious treatment for ED</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/uns8R4kENMs/nrurol.2012.74</link>
<description>A multicenter phase III trial of avanafil in 200 Korean men with erectile dysfunction has shown a significant improvement in patient erectile function at doses of 100 or 200 mg. During the 12-week trial, sexual function was assessed using patient questionnaires, including the International Index </description>
<content:encoded><![CDATA[

<p>
<b>Sexual dysfunction: Avanafil is a safe and efficacious treatment for ED</b>
</p>
<p>Nature Reviews Urology 9, 240 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.74">doi:10.1038/nrurol.2012.74</a>
</p>
<p>A multicenter phase III trial of avanafil in 200 Korean men with erectile dysfunction has shown a significant improvement in patient erectile function at doses of 100 or 200 mg. During the 12-week trial, sexual function was assessed using patient questionnaires, including the International Index </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/uns8R4kENMs" height="1" width="1"/>]]></content:encoded>
<dc:title>Sexual dysfunction: Avanafil is a safe and efficacious treatment for ED</dc:title>
<dc:identifier>doi:10.1038/nrurol.2012.74</dc:identifier>
<dc:source>Nature Reviews Urology 9, 240 (2012)</dc:source>
<dc:date>2012-04-17</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-17</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.74</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.74</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>240</prism:startingPage>
<prism:endingPage>240</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.74</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.75">
                     <title>Prostate cancer: Bevacizumab does not improve survival in mCRPC</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/fdem-kEV6nQ/nrurol.2012.75</link>
<description>Adding bevacizumab to standard docetaxel and prednisone therapy does not improve overall survival, despite improving progression-free survival and objective response, according to a randomized phase III clinical trial of 1,050 chemotherapy-naive men with metastatic castration-resistant prostate cancer. Importantly, treatment-related deaths were significantly more frequent in </description>
<content:encoded><![CDATA[

<p>
<b>Prostate cancer: Bevacizumab does not improve survival in mCRPC</b>
</p>
<p>Nature Reviews Urology 9, 240 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.75">doi:10.1038/nrurol.2012.75</a>
</p>
<p>Adding bevacizumab to standard docetaxel and prednisone therapy does not improve overall survival, despite improving progression-free survival and objective response, according to a randomized phase III clinical trial of 1,050 chemotherapy-naive men with metastatic castration-resistant prostate cancer. Importantly, treatment-related deaths were significantly more frequent in </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/fdem-kEV6nQ" height="1" width="1"/>]]></content:encoded>
<dc:title>Prostate cancer: Bevacizumab does not improve survival in mCRPC</dc:title>
<dc:identifier>doi:10.1038/nrurol.2012.75</dc:identifier>
<dc:source>Nature Reviews Urology 9, 240 (2012)</dc:source>
<dc:date>2012-04-17</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-17</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.75</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.75</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>240</prism:startingPage>
<prism:endingPage>240</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.75</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.76">
                     <title>BPH: New mouse model available for study</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/Dn2f_pXn5fg/nrurol.2012.76</link>
<description>New research has found that spontaneously hypertensive rats treated with testosterone simultaneously display erectile dysfunction, enlarged prostates and lower urinary tract symptoms—three common problems in ageing men. The discovery should help scientists study the adverse sexual effects of treatments for BPH and lower urinary tract </description>
<content:encoded><![CDATA[

<p>
<b>BPH: New mouse model available for study</b>
</p>
<p>Nature Reviews Urology 9, 240 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.76">doi:10.1038/nrurol.2012.76</a>
</p>
<p>New research has found that spontaneously hypertensive rats treated with testosterone simultaneously display erectile dysfunction, enlarged prostates and lower urinary tract symptoms&#8212;three common problems in ageing men. The discovery should help scientists study the adverse sexual effects of treatments for BPH and lower urinary tract </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/Dn2f_pXn5fg" height="1" width="1"/>]]></content:encoded>
<dc:title>BPH: New mouse model available for study</dc:title>
<dc:identifier>doi:10.1038/nrurol.2012.76</dc:identifier>
<dc:source>Nature Reviews Urology 9, 240 (2012)</dc:source>
<dc:date>2012-04-17</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-17</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.76</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.76</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>240</prism:startingPage>
<prism:endingPage>240</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.76</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.84">
                     <title>Bladder cancer: LASP-1—a promising urine marker for detection of bladder cancer</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/ZrRw6fzPYuc/nrurol.2012.84</link>
<description>LASP-1 (LIM and SH3 domain protein 1) is a focal adhesion protein that has previously been linked to cancers of the colon, ovary and breast. Now, in a study published in Urologic Oncology, a research team led by Peter Ardelt at the University of </description>
<content:encoded><![CDATA[

<p>
<b>Bladder cancer: LASP-1&#8212;a promising urine marker for detection of bladder cancer</b>
</p>
<p>Nature Reviews Urology 9, 240 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.84">doi:10.1038/nrurol.2012.84</a>
</p>
<p>Author: Sarah Payton</p>
<p>LASP-1 (LIM and SH3 domain protein 1) is a focal adhesion protein that has previously been linked to cancers of the colon, ovary and breast. Now, in a study published in Urologic Oncology, a research team led by Peter Ardelt at the University of </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/ZrRw6fzPYuc" height="1" width="1"/>]]></content:encoded>
<dc:title>Bladder cancer: LASP-1—a promising urine marker for detection of bladder cancer</dc:title>
<dc:creator>Sarah Payton</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.84</dc:identifier>
<dc:source>Nature Reviews Urology 9, 240 (2012)</dc:source>
<dc:date>2012-04-24</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-24</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.84</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.84</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Research Highlight</prism:section>
<prism:startingPage>240</prism:startingPage>
<prism:endingPage>240</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.84</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.78">
                     <title>Testicular cancer: Underestimating radiotherapy toxicity for stage I seminoma</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/9H0rwHnzr08/nrurol.2012.78</link>
<description>A recent survey of radiation oncologists has evaluated barriers to surveillance rather than adjuvant therapy for postorchiectomy management of stage I seminoma. The findings suggest that providers are underestimating the late toxicity of radiation therapy in these patients.</description>
<content:encoded><![CDATA[

<p>
<b>Testicular cancer: Underestimating radiotherapy toxicity for stage I seminoma</b>
</p>
<p>Nature Reviews Urology 9, 241 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.78">doi:10.1038/nrurol.2012.78</a>
</p>
<p>Authors: Nicklas Pfanzelter &amp; Justin E. Bekelman</p>
<p>A recent survey of radiation oncologists has evaluated barriers to surveillance rather than adjuvant therapy for postorchiectomy management of stage I seminoma. The findings suggest that providers are underestimating the late toxicity of radiation therapy in these patients.</p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/9H0rwHnzr08" height="1" width="1"/>]]></content:encoded>
<dc:title>Testicular cancer: Underestimating radiotherapy toxicity for stage I seminoma</dc:title>
<dc:creator>Nicklas Pfanzelter</dc:creator>
<dc:creator>Justin E. Bekelman</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.78</dc:identifier>
<dc:source>Nature Reviews Urology 9, 241 (2012)</dc:source>
<dc:date>2012-04-17</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-17</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.78</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.78</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>News and Views</prism:section>
<prism:startingPage>241</prism:startingPage>
<prism:endingPage>242</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.78</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.58">
                     <title>Urothelial carcinoma: Endoscopy to predict outcomes in upper tract urothelial cancer</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/gZz4fZChhD4/nrurol.2012.58</link>
<description>Cross-sectional imaging, endoscopic evaluation and biopsy are the mainstay of preoperative evaluation and staging of patients with upper tract urothelial carcinoma (UTUC), despite their limitations in accurate prediction of grade, stage and oncologic outcome. Multivariable models incorporating numerous clinical factors, including novel tumor markers will improve our ability to deliver personalized treatment.</description>
<content:encoded><![CDATA[

<p>
<b>Urothelial carcinoma: Endoscopy to predict outcomes in upper tract urothelial cancer</b>
</p>
<p>Nature Reviews Urology 9, 242 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.58">doi:10.1038/nrurol.2012.58</a>
</p>
<p>Authors: Ramy F. Youssef &amp; Vitaly Margulis</p>
<p>Cross-sectional imaging, endoscopic evaluation and biopsy are the mainstay of preoperative evaluation and staging of patients with upper tract urothelial carcinoma (UTUC), despite their limitations in accurate prediction of grade, stage and oncologic outcome. Multivariable models incorporating numerous clinical factors, including novel tumor markers will improve our ability to deliver personalized treatment.</p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/gZz4fZChhD4" height="1" width="1"/>]]></content:encoded>
<dc:title>Urothelial carcinoma: Endoscopy to predict outcomes in upper tract urothelial cancer</dc:title>
<dc:creator>Ramy F. Youssef</dc:creator>
<dc:creator>Vitaly Margulis</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.58</dc:identifier>
<dc:source>Nature Reviews Urology 9, 242 (2012)</dc:source>
<dc:date>2012-04-03</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-03</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.58</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.58</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>News and Views</prism:section>
<prism:startingPage>242</prism:startingPage>
<prism:endingPage>243</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.58</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.59">
                     <title>Urologic oncology: Poor trial accrual hinders germ cell tumor therapy advances</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/SH89IRp0lu4/nrurol.2012.59</link>
<description>In the last 3 years, three major trials involving patients with advanced germ cell testicular tumors have investigated dose-intense alternatives to standard BEP (bleomycin, etoposide, and cisplatin) therapy. All three trials failed to reach their accrual targets and none was able to demonstrate improved results.</description>
<content:encoded><![CDATA[

<p>
<b>Urologic oncology: Poor trial accrual hinders germ cell tumor therapy advances</b>
</p>
<p>Nature Reviews Urology 9, 243 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.59">doi:10.1038/nrurol.2012.59</a>
</p>
<p>Authors: Michael V. Williams &amp; Danish Mazhar</p>
<p>In the last 3 years, three major trials involving patients with advanced germ cell testicular tumors have investigated dose-intense alternatives to standard BEP (bleomycin, etoposide, and cisplatin) therapy. All three trials failed to reach their accrual targets and none was able to demonstrate improved results.</p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/SH89IRp0lu4" height="1" width="1"/>]]></content:encoded>
<dc:title>Urologic oncology: Poor trial accrual hinders germ cell tumor therapy advances</dc:title>
<dc:creator>Michael V. Williams</dc:creator>
<dc:creator>Danish Mazhar</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.59</dc:identifier>
<dc:source>Nature Reviews Urology 9, 243 (2012)</dc:source>
<dc:date>2012-04-03</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-03</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.59</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.59</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>News and Views</prism:section>
<prism:startingPage>243</prism:startingPage>
<prism:endingPage>245</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.59</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.79">
                     <title>Prostate cancer: Bone Scan Index made easy, at last</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/hmGFaznQ2-c/nrurol.2012.79</link>
<description>The Bone Scan Index (BSI) is a methodology used to quantify bone metastases and monitor changes under treatment. However, BSI is manually calculated and is, therefore, tedious and time-consuming to use, so it is not routinely implemented. A new automated platform to calculate BSI should help to increase its use.</description>
<content:encoded><![CDATA[

<p>
<b>Prostate cancer: Bone Scan Index made easy, at last</b>
</p>
<p>Nature Reviews Urology 9, 245 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.79">doi:10.1038/nrurol.2012.79</a>
</p>
<p>Author: Bertrand Tombal</p>
<p>The Bone Scan Index (BSI) is a methodology used to quantify bone metastases and monitor changes under treatment. However, BSI is manually calculated and is, therefore, tedious and time-consuming to use, so it is not routinely implemented. A new automated platform to calculate BSI should help to increase its use.</p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/hmGFaznQ2-c" height="1" width="1"/>]]></content:encoded>
<dc:title>Prostate cancer: Bone Scan Index made easy, at last</dc:title>
<dc:creator>Bertrand Tombal</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.79</dc:identifier>
<dc:source>Nature Reviews Urology 9, 245 (2012)</dc:source>
<dc:date>2012-04-24</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-24</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.79</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.79</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>News and Views</prism:section>
<prism:startingPage>245</prism:startingPage>
<prism:endingPage>246</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.79</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.41">
                     <title>The hemodynamic approach to evaluating adolescent varicocele</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/E2k0Mrez80Y/nrurol.2012.41</link>
<description>During adolescence, the risk of developing a varicocele increases. Prevalence is less than 1% in boys aged younger than 10 years, but approaches that of the general adult population (about 15%) during puberty. For adolescent males with varicoceles, surgical risk factors have not yet been </description>
<content:encoded><![CDATA[

<p>
<b>The hemodynamic approach to evaluating adolescent varicocele</b>
</p>
<p>Nature Reviews Urology 9, 247 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.41">doi:10.1038/nrurol.2012.41</a>
</p>
<p>Authors: Marcello Cimador, Marco Castagnetti, Ignazio Gattuccio, Marco Pensabene, Maria Sergio &amp; Enrico De Grazia</p>
<p>During adolescence, the risk of developing a varicocele increases. Prevalence is less than 1% in boys aged younger than 10 years, but approaches that of the general adult population (about 15%) during puberty. For adolescent males with varicoceles, surgical risk factors have not yet been </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/E2k0Mrez80Y" height="1" width="1"/>]]></content:encoded>
<dc:title>The hemodynamic approach to evaluating adolescent varicocele</dc:title>
<dc:creator>Marcello Cimador</dc:creator>
<dc:creator>Marco Castagnetti</dc:creator>
<dc:creator>Ignazio Gattuccio</dc:creator>
<dc:creator>Marco Pensabene</dc:creator>
<dc:creator>Maria Sergio</dc:creator>
<dc:creator>Enrico De Grazia</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.41</dc:identifier>
<dc:source>Nature Reviews Urology 9, 247 (2012)</dc:source>
<dc:date>2012-03-27</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-03-27</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.41</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.41</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>247</prism:startingPage>
<prism:endingPage>257</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.41</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.56">
                     <title>The effect of ethnicity and sexual preference on prostate-cancer-related quality of life</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/PjAuKocuHmY/nrurol.2012.56</link>
<description>In general, patients with prostate cancer are able to maintain a relatively high quality of life (QOL), commonly reporting improvements in physical, emotional, and social functioning within 1 year of treatment. However, certain subpopulations of patients are susceptible to significant reductions in QOL during the </description>
<content:encoded><![CDATA[

<p>
<b>The effect of ethnicity and sexual preference on prostate-cancer-related quality of life</b>
</p>
<p>Nature Reviews Urology 9, 258 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.56">doi:10.1038/nrurol.2012.56</a>
</p>
<p>Authors: Nir Kleinmann, Nicholas G. Zaorsky, Timothy N. Showalter, Leonard G. Gomella, Costas D. Lallas &amp; Edouard J. Trabulsi</p>
<p>In general, patients with prostate cancer are able to maintain a relatively high quality of life (QOL), commonly reporting improvements in physical, emotional, and social functioning within 1 year of treatment. However, certain subpopulations of patients are susceptible to significant reductions in QOL during the </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/PjAuKocuHmY" height="1" width="1"/>]]></content:encoded>
<dc:title>The effect of ethnicity and sexual preference on prostate-cancer-related quality of life</dc:title>
<dc:creator>Nir Kleinmann</dc:creator>
<dc:creator>Nicholas G. Zaorsky</dc:creator>
<dc:creator>Timothy N. Showalter</dc:creator>
<dc:creator>Leonard G. Gomella</dc:creator>
<dc:creator>Costas D. Lallas</dc:creator>
<dc:creator>Edouard J. Trabulsi</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.56</dc:identifier>
<dc:source>Nature Reviews Urology 9, 258 (2012)</dc:source>
<dc:date>2012-04-10</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-10</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.56</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.56</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>258</prism:startingPage>
<prism:endingPage>265</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.56</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.57">
                     <title>Perioperative chemotherapy for upper tract urothelial cancer</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/pfuHhMDkLCk/nrurol.2012.57</link>
<description>Upper tract urothelial cancer (UTUC) is an aggressive disease associated with significant morbidity and mortality. Radical nephroureterectomy (RNU) with bladder cuff removal is considered the standard of care for most invasive UTUCs but distant relapses after surgery for locally advanced, high-grade disease are common. Although </description>
<content:encoded><![CDATA[

<p>
<b>Perioperative chemotherapy for upper tract urothelial cancer</b>
</p>
<p>Nature Reviews Urology 9, 266 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.57">doi:10.1038/nrurol.2012.57</a>
</p>
<p>Authors: Ajjai S. Alva, Surena F. Matin, Seth P. Lerner &amp; Arlene O. Siefker-Radtke</p>
<p>Upper tract urothelial cancer (UTUC) is an aggressive disease associated with significant morbidity and mortality. Radical nephroureterectomy (RNU) with bladder cuff removal is considered the standard of care for most invasive UTUCs but distant relapses after surgery for locally advanced, high-grade disease are common. Although </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/pfuHhMDkLCk" height="1" width="1"/>]]></content:encoded>
<dc:title>Perioperative chemotherapy for upper tract urothelial cancer</dc:title>
<dc:creator>Ajjai S. Alva</dc:creator>
<dc:creator>Surena F. Matin</dc:creator>
<dc:creator>Seth P. Lerner</dc:creator>
<dc:creator>Arlene O. Siefker-Radtke</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.57</dc:identifier>
<dc:source>Nature Reviews Urology 9, 266 (2012)</dc:source>
<dc:date>2012-04-10</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-04-10</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.57</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.57</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>266</prism:startingPage>
<prism:endingPage>273</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.57</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.14">
                     <title>The role of connexins in prostate cancer promotion and progression</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/j8UQP9p8W40/nrurol.2012.14</link>
<description>Prostate cancer is a prevalent disease that is characterized by a presumably long latency period and a moderate propensity to metastasize. Although a range of mechanisms have been implicated in prostate carcinogenesis, the factors determining the initiation of metastasis remain obscure. The synchronized function of </description>
<content:encoded><![CDATA[

<p>
<b>The role of connexins in prostate cancer promotion and progression</b>
</p>
<p>Nature Reviews Urology 9, 274 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.14">doi:10.1038/nrurol.2012.14</a>
</p>
<p>Authors: Jaros&#322;aw Czy&#380;, Katarzyna Szpak &amp; Zbigniew Madeja</p>
<p>Prostate cancer is a prevalent disease that is characterized by a presumably long latency period and a moderate propensity to metastasize. Although a range of mechanisms have been implicated in prostate carcinogenesis, the factors determining the initiation of metastasis remain obscure. The synchronized function of </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/j8UQP9p8W40" height="1" width="1"/>]]></content:encoded>
<dc:title>The role of connexins in prostate cancer promotion and progression</dc:title>
<dc:creator>Jarosław Czyż</dc:creator>
<dc:creator>Katarzyna Szpak</dc:creator>
<dc:creator>Zbigniew Madeja</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.14</dc:identifier>
<dc:source>Nature Reviews Urology 9, 274 (2012)</dc:source>
<dc:date>2012-02-21</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-02-21</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.14</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.14</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Review</prism:section>
<prism:startingPage>274</prism:startingPage>
<prism:endingPage>282</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.14</feedburner:origLink></item>
<item rdf:about="http://dx.doi.org/10.1038/nrurol.2012.33">
                     <title>The role of prostanoids in urinary bladder physiology</title>
<link>http://feeds.nature.com/~r/nrurol/rss/current/~3/XFXV1GToX64/nrurol.2012.33</link>
<description>Five primary prostanoids are synthesized by the cyclooxygenase enzymes, COX-1 and COX-2: the prostaglandins PGE2, PGF2α, PGI2, PGD2 and thromboxane A2. High levels of these signaling molecules have been implicated—in both animal models and human studies—in decreased </description>
<content:encoded><![CDATA[

<p>
<b>The role of prostanoids in urinary bladder physiology</b>
</p>
<p>Nature Reviews Urology 9, 283 (2012).  
            <a href="http://dx.doi.org/10.1038/nrurol.2012.33">doi:10.1038/nrurol.2012.33</a>
</p>
<p>Authors: Mohammad S. Rahnama'i, Philip E. V. van Kerrebroeck, Stefan G. de Wachter &amp; Gommert A. van Koeveringe</p>
<p>Five primary prostanoids are synthesized by the cyclooxygenase enzymes, COX-1 and COX-2: the prostaglandins PGE2, PGF2&#945;, PGI2, PGD2 and thromboxane A2. High levels of these signaling molecules have been implicated&#8212;in both animal models and human studies&#8212;in decreased </p>
<img src="http://feeds.feedburner.com/~r/nrurol/rss/current/~4/XFXV1GToX64" height="1" width="1"/>]]></content:encoded>
<dc:title>The role of prostanoids in urinary bladder physiology</dc:title>
<dc:creator>Mohammad S. Rahnama'i</dc:creator>
<dc:creator>Philip E. V. van Kerrebroeck</dc:creator>
<dc:creator>Stefan G. de Wachter</dc:creator>
<dc:creator>Gommert A. van Koeveringe</dc:creator>
<dc:identifier>doi:10.1038/nrurol.2012.33</dc:identifier>
<dc:source>Nature Reviews Urology 9, 283 (2012)</dc:source>
<dc:date>2012-03-13</dc:date>
<prism:publicationName>Nature Reviews Urology</prism:publicationName>
<prism:publicationDate>2012-03-13</prism:publicationDate>
<prism:doi>10.1038/nrurol.2012.33</prism:doi>
<prism:url>http://dx.doi.org/10.1038/nrurol.2012.33</prism:url>
<prism:volume>9</prism:volume>
<prism:number>5</prism:number>
<prism:section>Perspectives</prism:section>
<prism:startingPage>283</prism:startingPage>
<prism:endingPage>290</prism:endingPage>
<feedburner:origLink>http://dx.doi.org/10.1038/nrurol.2012.33</feedburner:origLink></item>
</rdf:RDF>

