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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Veröffentlicht in:Scientific reports 2016-03, Vol.6 (1), p.23135-23135, Article 23135
Hauptverfasser: 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
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container_issue 1
container_start_page 23135
container_title Scientific reports
container_volume 6
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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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. 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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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