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Methylseleninic acid downregulates hypoxia‐inducible factor‐1α in invasive prostate cancer
Author(s) -
Sinha Indu,
Kevin,
Wolter William,
Suckow Mark A.,
King Tonya,
Pinto John T.,
Sinha Raghu
Publication year - 2011
Publication title -
international journal of cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.475
H-Index - 234
eISSN - 1097-0215
pISSN - 0020-7136
DOI - 10.1002/ijc.26141
Subject(s) - du145 , prostate cancer , prostate , medicine , endocrinology , cancer , cancer research , in vivo , hypoxia (environmental) , cancer cell , biology , chemistry , lncap , microbiology and biotechnology , organic chemistry , oxygen
Abstract Alternative strategies are needed to control growth of advanced and hormone refractory prostate cancer. In this regard, we investigated the efficacy of methylseleninic acid (MSeA), a penultimate precursor to the highly reactive selenium metabolite, methylselenol, to inhibit growth of invasive and hormone refractory rat (PAIII) and human (PC‐3 and PC‐3M) prostate cancer cells. Our results demonstrate that MSeA inhibits PAIII cell growth in vitro as well as reduces weights of tumors generated by PAIII cells treated ex vivo . A significant reduction in the number of metastatic lung foci by MSeA treatment was also noted in Lobund‐Wistar rats. The PAIII cells along with PC‐3, DU145 and PC‐3M cells undergo apoptosis after MSeA treatments in both normoxia and hypoxia. Treatment of metastatic rat and human prostate cancer cell lines with MSeA decreased hypoxia‐inducible factor‐1α (HIF‐1α) levels in a dose‐dependent manner. Additionally, HIF‐1α transcription activity both in normoxic and hypoxic conditions is reduced after MSeA treatment of prostate cancer cells. Furthermore, VEGF and GLUT1, downstream targets of HIF‐1α, were also reduced in prostate cancer cells after MSeA treatment. Our study illustrates the efficacy of MSeA in controlling growth of hormone refractory prostate cancer by downregulating HIF‐1α, which is possibly occurring through stabilization or increase in prolyl hydroxylase activity.