Graviola inhibits hypoxia-induced NADPH oxidase activity in prostate cancer cells reducing their proliferation and clonogenicity
Prostate cancer (PCa) is the leading malignancy among men. Importantly, this disease is mostly diagnosed at early stages offering a unique chemoprevention opportunity. Therefore, there is an urgent need to identify and target signaling molecules with higher expression/activity in prostate tumors and...
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creator | Deep, Gagan Kumar, Rahul Jain, Anil K. Dhar, Deepanshi Panigrahi, Gati K. Hussain, Anowar Agarwal, Chapla El-Elimat, Tamam Sica, Vincent P. Oberlies, Nicholas H. Agarwal, Rajesh |
description | Prostate cancer (PCa) is the leading malignancy among men. Importantly, this disease is mostly diagnosed at early stages offering a unique chemoprevention opportunity. Therefore, there is an urgent need to identify and target signaling molecules with higher expression/activity in prostate tumors and play critical role in PCa growth and progression. Here we report that NADPH oxidase (NOX) expression is directly associated with PCa progression in TRAMP mice, suggesting NOX as a potential chemoprevention target in controlling PCa. Accordingly, we assessed whether NOX activity in PCa cells could be inhibited by Graviola pulp extract (GPE) that contains unique acetogenins with strong anti-cancer effects. GPE (1–5 μg/ml) treatment strongly inhibited the hypoxia-induced NOX activity in PCa cells (LNCaP, 22Rv1 and PC3) associated with a decrease in the expression of NOX catalytic and regulatory sub-units (NOX1, NOX2 and p47
phox
). Furthermore, GPE-mediated NOX inhibition was associated with a strong decrease in nuclear HIF-1α levels as well as reduction in the proliferative and clonogenic potential of PCa cells. More importantly, GPE treatment neither inhibited NOX activity nor showed any cytotoxicity against non-neoplastic prostate epithelial PWR-1E cells. Overall, these results suggest that GPE could be useful in the prevention of PCa progression via inhibiting NOX activity. |
doi_str_mv | 10.1038/srep23135 |
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phox
). Furthermore, GPE-mediated NOX inhibition was associated with a strong decrease in nuclear HIF-1α levels as well as reduction in the proliferative and clonogenic potential of PCa cells. More importantly, GPE treatment neither inhibited NOX activity nor showed any cytotoxicity against non-neoplastic prostate epithelial PWR-1E cells. Overall, these results suggest that GPE could be useful in the prevention of PCa progression via inhibiting NOX activity.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep23135</identifier><identifier>PMID: 26979487</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13/1 ; 13/95 ; 38/39 ; 631/67/2195 ; 631/67/327 ; 631/67/589/466 ; 692/4028/67/589/466 ; Adenocarcinoma - drug therapy ; Adenocarcinoma - enzymology ; Animals ; Annonaceae - chemistry ; Antineoplastic Agents, Phytogenic - pharmacology ; Cell Hypoxia ; Cell Line, Tumor ; Cell proliferation ; Cell Proliferation - drug effects ; Cell Survival - drug effects ; CYBB protein ; Cytotoxicity ; Humanities and Social Sciences ; Humans ; Hypoxia ; Male ; Malignancy ; Membrane Glycoproteins - metabolism ; Mice, Transgenic ; multidisciplinary ; NAD(P)H oxidase ; NADH, NADPH Oxidoreductases - metabolism ; NADPH Oxidase 1 ; NADPH Oxidase 2 ; NADPH Oxidases - metabolism ; Plant Extracts - pharmacology ; Prostate cancer ; Prostatic Neoplasms - drug therapy ; Prostatic Neoplasms - enzymology ; Science ; Science (multidisciplinary) ; Tumors</subject><ispartof>Scientific reports, 2016-03, Vol.6 (1), p.23135-23135, Article 23135</ispartof><rights>The Author(s) 2016</rights><rights>Copyright Nature Publishing Group Mar 2016</rights><rights>Copyright © 2016, Macmillan Publishers Limited 2016 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-dee4fa7e3c00743e9b054feb68f1a439f8fdc91e5d1ac09bed80fc6fc3b7ee123</citedby><cites>FETCH-LOGICAL-c438t-dee4fa7e3c00743e9b054feb68f1a439f8fdc91e5d1ac09bed80fc6fc3b7ee123</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793251/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793251/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,41120,42189,51576,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26979487$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Deep, Gagan</creatorcontrib><creatorcontrib>Kumar, Rahul</creatorcontrib><creatorcontrib>Jain, Anil K.</creatorcontrib><creatorcontrib>Dhar, Deepanshi</creatorcontrib><creatorcontrib>Panigrahi, Gati K.</creatorcontrib><creatorcontrib>Hussain, Anowar</creatorcontrib><creatorcontrib>Agarwal, Chapla</creatorcontrib><creatorcontrib>El-Elimat, Tamam</creatorcontrib><creatorcontrib>Sica, Vincent P.</creatorcontrib><creatorcontrib>Oberlies, Nicholas H.</creatorcontrib><creatorcontrib>Agarwal, Rajesh</creatorcontrib><title>Graviola inhibits hypoxia-induced NADPH oxidase activity in prostate cancer cells reducing their proliferation and clonogenicity</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><addtitle>Sci Rep</addtitle><description>Prostate cancer (PCa) is the leading malignancy among men. Importantly, this disease is mostly diagnosed at early stages offering a unique chemoprevention opportunity. Therefore, there is an urgent need to identify and target signaling molecules with higher expression/activity in prostate tumors and play critical role in PCa growth and progression. Here we report that NADPH oxidase (NOX) expression is directly associated with PCa progression in TRAMP mice, suggesting NOX as a potential chemoprevention target in controlling PCa. Accordingly, we assessed whether NOX activity in PCa cells could be inhibited by Graviola pulp extract (GPE) that contains unique acetogenins with strong anti-cancer effects. GPE (1–5 μg/ml) treatment strongly inhibited the hypoxia-induced NOX activity in PCa cells (LNCaP, 22Rv1 and PC3) associated with a decrease in the expression of NOX catalytic and regulatory sub-units (NOX1, NOX2 and p47
phox
). Furthermore, GPE-mediated NOX inhibition was associated with a strong decrease in nuclear HIF-1α levels as well as reduction in the proliferative and clonogenic potential of PCa cells. More importantly, GPE treatment neither inhibited NOX activity nor showed any cytotoxicity against non-neoplastic prostate epithelial PWR-1E cells. Overall, these results suggest that GPE could be useful in the prevention of PCa progression via inhibiting NOX activity.</description><subject>13/1</subject><subject>13/95</subject><subject>38/39</subject><subject>631/67/2195</subject><subject>631/67/327</subject><subject>631/67/589/466</subject><subject>692/4028/67/589/466</subject><subject>Adenocarcinoma - drug therapy</subject><subject>Adenocarcinoma - enzymology</subject><subject>Animals</subject><subject>Annonaceae - chemistry</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>Cell Hypoxia</subject><subject>Cell Line, Tumor</subject><subject>Cell proliferation</subject><subject>Cell Proliferation - drug effects</subject><subject>Cell Survival - drug effects</subject><subject>CYBB protein</subject><subject>Cytotoxicity</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Hypoxia</subject><subject>Male</subject><subject>Malignancy</subject><subject>Membrane Glycoproteins - metabolism</subject><subject>Mice, Transgenic</subject><subject>multidisciplinary</subject><subject>NAD(P)H oxidase</subject><subject>NADH, NADPH Oxidoreductases - metabolism</subject><subject>NADPH Oxidase 1</subject><subject>NADPH Oxidase 2</subject><subject>NADPH Oxidases - metabolism</subject><subject>Plant Extracts - pharmacology</subject><subject>Prostate cancer</subject><subject>Prostatic Neoplasms - drug therapy</subject><subject>Prostatic Neoplasms - enzymology</subject><subject>Science</subject><subject>Science (multidisciplinary)</subject><subject>Tumors</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNplkU9vFCEYxifGxjZtD34BQ-LFNhmFgRngYtLU2po06kHPhGFedmlmYQRm49760ctm62ZVLhDe3_u8f56qek3we4Kp-JAiTA0ltH1RnTSYtXVDm-blwfu4Ok_pAZfTNpIR-ao6bjrJJRP8pHq8jXrtwqiR80vXu5zQcjOF307Xzg-zgQF9vfr0_Q6Vr0EnQNpkt3Z5U3g0xZCyzoCM9gYiMjCOCUUoec4vUF6Ci1todBaizi54pP2AzBh8WIB3puicVUdWjwnOn-_T6ufnmx_Xd_X9t9sv11f3tWFU5HoAYFZzoAZjzijIHrfMQt8JSzSj0go7GEmgHYg2WPYwCGxNZw3tOQBp6Gn1cac7zf0KBgM-Rz2qKbqVjhsVtFN_R7xbqkVYK8YlbVpSBN49C8Twa4aU1cql7cTaQ5iTIpwz0uG2bQv69h_0IczRl_EUEVJ0omNcFOpiR5myxuKi3TdDsNpaq_bWFvbNYfd78o-RBbjcAamE_ALiQcn_1J4AXDSyDA</recordid><startdate>20160316</startdate><enddate>20160316</enddate><creator>Deep, Gagan</creator><creator>Kumar, Rahul</creator><creator>Jain, Anil K.</creator><creator>Dhar, Deepanshi</creator><creator>Panigrahi, Gati K.</creator><creator>Hussain, Anowar</creator><creator>Agarwal, Chapla</creator><creator>El-Elimat, Tamam</creator><creator>Sica, Vincent P.</creator><creator>Oberlies, Nicholas H.</creator><creator>Agarwal, Rajesh</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160316</creationdate><title>Graviola inhibits hypoxia-induced NADPH oxidase activity in prostate cancer cells reducing their proliferation and clonogenicity</title><author>Deep, Gagan ; Kumar, Rahul ; Jain, Anil K. ; Dhar, Deepanshi ; Panigrahi, Gati K. ; Hussain, Anowar ; Agarwal, Chapla ; El-Elimat, Tamam ; Sica, Vincent P. ; Oberlies, Nicholas H. ; Agarwal, Rajesh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-dee4fa7e3c00743e9b054feb68f1a439f8fdc91e5d1ac09bed80fc6fc3b7ee123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>13/1</topic><topic>13/95</topic><topic>38/39</topic><topic>631/67/2195</topic><topic>631/67/327</topic><topic>631/67/589/466</topic><topic>692/4028/67/589/466</topic><topic>Adenocarcinoma - drug therapy</topic><topic>Adenocarcinoma - enzymology</topic><topic>Animals</topic><topic>Annonaceae - chemistry</topic><topic>Antineoplastic Agents, Phytogenic - pharmacology</topic><topic>Cell Hypoxia</topic><topic>Cell Line, Tumor</topic><topic>Cell proliferation</topic><topic>Cell Proliferation - drug effects</topic><topic>Cell Survival - drug effects</topic><topic>CYBB protein</topic><topic>Cytotoxicity</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Hypoxia</topic><topic>Male</topic><topic>Malignancy</topic><topic>Membrane Glycoproteins - metabolism</topic><topic>Mice, Transgenic</topic><topic>multidisciplinary</topic><topic>NAD(P)H oxidase</topic><topic>NADH, NADPH Oxidoreductases - metabolism</topic><topic>NADPH Oxidase 1</topic><topic>NADPH Oxidase 2</topic><topic>NADPH Oxidases - metabolism</topic><topic>Plant Extracts - pharmacology</topic><topic>Prostate cancer</topic><topic>Prostatic Neoplasms - drug therapy</topic><topic>Prostatic Neoplasms - enzymology</topic><topic>Science</topic><topic>Science (multidisciplinary)</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Deep, Gagan</creatorcontrib><creatorcontrib>Kumar, Rahul</creatorcontrib><creatorcontrib>Jain, Anil K.</creatorcontrib><creatorcontrib>Dhar, Deepanshi</creatorcontrib><creatorcontrib>Panigrahi, Gati K.</creatorcontrib><creatorcontrib>Hussain, Anowar</creatorcontrib><creatorcontrib>Agarwal, Chapla</creatorcontrib><creatorcontrib>El-Elimat, Tamam</creatorcontrib><creatorcontrib>Sica, Vincent P.</creatorcontrib><creatorcontrib>Oberlies, Nicholas H.</creatorcontrib><creatorcontrib>Agarwal, Rajesh</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Scientific reports</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Deep, Gagan</au><au>Kumar, Rahul</au><au>Jain, Anil K.</au><au>Dhar, Deepanshi</au><au>Panigrahi, Gati K.</au><au>Hussain, Anowar</au><au>Agarwal, Chapla</au><au>El-Elimat, Tamam</au><au>Sica, Vincent P.</au><au>Oberlies, Nicholas H.</au><au>Agarwal, Rajesh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Graviola inhibits hypoxia-induced NADPH oxidase activity in prostate cancer cells reducing their proliferation and clonogenicity</atitle><jtitle>Scientific reports</jtitle><stitle>Sci Rep</stitle><addtitle>Sci Rep</addtitle><date>2016-03-16</date><risdate>2016</risdate><volume>6</volume><issue>1</issue><spage>23135</spage><epage>23135</epage><pages>23135-23135</pages><artnum>23135</artnum><issn>2045-2322</issn><eissn>2045-2322</eissn><abstract>Prostate cancer (PCa) is the leading malignancy among men. Importantly, this disease is mostly diagnosed at early stages offering a unique chemoprevention opportunity. Therefore, there is an urgent need to identify and target signaling molecules with higher expression/activity in prostate tumors and play critical role in PCa growth and progression. Here we report that NADPH oxidase (NOX) expression is directly associated with PCa progression in TRAMP mice, suggesting NOX as a potential chemoprevention target in controlling PCa. Accordingly, we assessed whether NOX activity in PCa cells could be inhibited by Graviola pulp extract (GPE) that contains unique acetogenins with strong anti-cancer effects. GPE (1–5 μg/ml) treatment strongly inhibited the hypoxia-induced NOX activity in PCa cells (LNCaP, 22Rv1 and PC3) associated with a decrease in the expression of NOX catalytic and regulatory sub-units (NOX1, NOX2 and p47
phox
). Furthermore, GPE-mediated NOX inhibition was associated with a strong decrease in nuclear HIF-1α levels as well as reduction in the proliferative and clonogenic potential of PCa cells. More importantly, GPE treatment neither inhibited NOX activity nor showed any cytotoxicity against non-neoplastic prostate epithelial PWR-1E cells. Overall, these results suggest that GPE could be useful in the prevention of PCa progression via inhibiting NOX activity.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>26979487</pmid><doi>10.1038/srep23135</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 13/1 13/95 38/39 631/67/2195 631/67/327 631/67/589/466 692/4028/67/589/466 Adenocarcinoma - drug therapy Adenocarcinoma - enzymology Animals Annonaceae - chemistry Antineoplastic Agents, Phytogenic - pharmacology Cell Hypoxia Cell Line, Tumor Cell proliferation Cell Proliferation - drug effects Cell Survival - drug effects CYBB protein Cytotoxicity Humanities and Social Sciences Humans Hypoxia Male Malignancy Membrane Glycoproteins - metabolism Mice, Transgenic multidisciplinary NAD(P)H oxidase NADH, NADPH Oxidoreductases - metabolism NADPH Oxidase 1 NADPH Oxidase 2 NADPH Oxidases - metabolism Plant Extracts - pharmacology Prostate cancer Prostatic Neoplasms - drug therapy Prostatic Neoplasms - enzymology Science Science (multidisciplinary) Tumors |
title | Graviola inhibits hypoxia-induced NADPH oxidase activity in prostate cancer cells reducing their proliferation and clonogenicity |
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