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Peroxisome proliferator-activated receptor γ and colorectal cancer

机译:过氧化物酶体增殖物激活受体γ与大肠癌

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摘要

Peroxisome proliferator-activated receptors (PPARs) are members of the nuclear hormone receptor superfamily and ligand-activated transcription factors. PPARγ plays an important role in adipocyte differentiation, lipid storage and energy dissipation in adipose tissue, and is involved in the control of inflammatory reactions as well as in glucose metabolism through the improvement of insulin sensitivity. Growing evidence has demonstrated that activation of PPARγ has an antineoplastic effect in tumors, including colorectal cancer. High expression of PPARγ is detected in human colon cancer cell lines and adenocarcinoma. This review describes the molecular mechanisms by which PPARγ regulates tumorigenesis in colorectal cancer, and examines current clinical trials evaluating PPARγ agonists as therapeutic agents for colorectal cancer.
机译:过氧化物酶体增殖物激活受体(PPAR)是核激素受体超家族和配体激活的转录因子的成员。 PPARγ在脂肪组织的脂肪细胞分化,脂质存储和能量耗散中起重要作用,并且通过改善胰岛素敏感性参与炎症反应的控制以及葡萄糖代谢。越来越多的证据表明,PPARγ的激活在包括大肠癌在内的肿瘤中具有抗肿瘤作用。在人结肠癌细胞系和腺癌中检测到PPARγ的高表达。这篇综述描述了PPARγ调节大肠癌肿瘤发生的分子机制,并审查了目前评价PPARγ激动剂作为大肠癌治疗剂的临床试验。

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