Thiazolidinediones as anti-cancer agents.

Cancer therapy Pub Date : 2008-01-01
Carmelo Blanquicett, Jesse Roman, C Michael Hart
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引用次数: 0

Abstract

The PPAR-gamma (PPAR-γ) activating thiazolidinedione (TZD) medications are a class of drugs used to improve lipid and glucose metabolism in type-2 diabetes. In addition to their known insulin sensitization action, these drugs have been shown to suppress tumor development in several in vitro and in vivo models. Among the proposed mechanisms for the anti-tumor effects of TZDs, apoptosis induction, cell cycle arrest, and differentiation have been extensively reported. Interestingly, some of the observed anti-tumor effects are independent of PPAR-γ activation. The following review will discuss studies employing TZDs as anti-cancer therapies for the most common types of cancers including, lung, breast, and colon and will explore the principal PPAR-γ-dependent and -independent mechanisms by which TZDs exert their anti-tumor effects.

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噻唑烷二酮类抗癌药物。
PPAR-γ (PPAR-γ)激活噻唑烷二酮(TZD)药物是一类用于改善2型糖尿病患者脂质和葡萄糖代谢的药物。除了已知的胰岛素增敏作用外,这些药物还在一些体外和体内模型中显示出抑制肿瘤发展的作用。在被提出的TZDs抗肿瘤作用机制中,诱导凋亡、细胞周期阻滞和分化已被广泛报道。有趣的是,一些观察到的抗肿瘤作用与PPAR-γ激活无关。下面的综述将讨论利用TZDs作为最常见类型癌症(包括肺癌、乳腺癌和结肠癌)的抗癌疗法的研究,并将探讨TZDs发挥其抗肿瘤作用的主要依赖和不依赖PPAR-γ的机制。
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