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Aminomethylphosphonic acid and methoxyacetic acid induce apoptosis in prostate cancer cells.
Int J Mol Sci ; 16(5): 11750-65, 2015 May 22.
Article en En | MEDLINE | ID: mdl-26006246
Aminomethylphosphonic acid (AMPA) and its parent compound herbicide glyphosate are analogs to glycine, which have been reported to inhibit proliferation and promote apoptosis of cancer cells, but not normal cells. Methoxyacetic acid (MAA) is the active metabolite of ester phthalates widely used in industry as gelling, viscosity and stabilizer; its exposure is associated with developmental and reproductive toxicities in both rodents and humans. MAA has been reported to suppress prostate cancer cell growth by inducing growth arrest and apoptosis. However, it is unknown whether AMPA and MAA can inhibit cancer cell growth. In this study, we found that AMPA and MAA inhibited cell growth in prostate cancer cell lines (LNCaP, C4-2B, PC-3 and DU-145) through induction of apoptosis and cell cycle arrest at the G1 phase. Importantly, the AMPA-induced apoptosis was potentiated with the addition of MAA, which was due to downregulation of the anti-apoptotic gene baculoviral inhibitor of apoptosis protein repeat containing 2 (BIRC2), leading to activation of caspases 7 and 3. These results demonstrate that the combination of AMPA and MAA can promote the apoptosis of prostate cancer cells, suggesting that they can be used as potential therapeutic drugs in the treatment of prostate cancer.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Próstata / Neoplasias de la Próstata / Protocolos de Quimioterapia Combinada Antineoplásica / Apoptosis / Organofosfonatos / Acetatos / Antineoplásicos Límite: Humans / Male Idioma: En Revista: Int J Mol Sci Año: 2015 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Próstata / Neoplasias de la Próstata / Protocolos de Quimioterapia Combinada Antineoplásica / Apoptosis / Organofosfonatos / Acetatos / Antineoplásicos Límite: Humans / Male Idioma: En Revista: Int J Mol Sci Año: 2015 Tipo del documento: Article