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The role of peroxisome proliferator-activated receptor gamma in prostate cancer

机译:过氧化物酶体增殖物激活受体γ在前列腺癌中的作用

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摘要

Despite great progress in the detection and treatment of prostate cancer, this disease remains an incredible health and economic burden. Although androgen receptor (AR) signaling plays a key role in the development and progression of prostate cancer, aberrations in other molecular pathways also contribute to the disease, making it essential to identify and develop drugs against novel targets, both for the prevention and treatment of prostate cancer. One promising target is the peroxisome proliferator-activated receptor gamma (PPARγ) protein. PPARγ was originally thought to act as a tumor suppressor in prostate cells because agonist ligands inhibited the growth of prostate cancer cells; however, additional studies found that PPARγ agonists inhibit cell growth independent of PPARγ. Furthermore, PPARγ expression increases with cancer grade/stage, which would suggest that it is not a tumor suppressor but instead that PPARγ activity may play a role in prostate cancer development and/or progression. Indeed, two new studies, taking vastly different, unbiased approaches, have identified PPARγ as a target in prostate cancer and suggest that PPARγ inhibition might be useful in prostate cancer prevention and treatment. These findings could lead to a new therapeutic weapon in the fight against prostate cancer.
机译:尽管在前列腺癌的检测和治疗方面取得了长足的进步,但这种疾病仍然是令人难以置信的健康和经济负担。尽管雄激素受体(AR)信号在前列腺癌的发展和进程中起着关键作用,但其他分子途径中的畸变也有助于该疾病的发展,因此对于预防和治疗新型靶标,鉴定和开发针对新型靶标的药物至关重要。前列腺癌。一个有希望的目标是过氧化物酶体增殖物激活受体γ(PPARγ)蛋白。最初认为PPARγ在前列腺细胞中起抑癌作用,因为激动剂配体会抑制前列腺癌细胞的生长。但是,其他研究发现,PPARγ激动剂可独立于PPARγ抑制细胞生长。此外,PPARγ表达随癌症等级/阶段而增加,这表明它不是肿瘤抑制因子,而是PPARγ活性可能在前列腺癌的发展和/或进展中起作用。确实,两项新的研究采用了截然不同的,无偏见的方法,已将PPARγ鉴定为前列腺癌的靶标,并表明PPARγ抑制作用可能对前列腺癌的预防和治疗有用。这些发现可能会导致对抗前列腺癌的新治疗武器。

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