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Peroxisome proliferator-activated receptor-gamma ligands for the treatment of breast cancer.

机译:过氧化物酶体增殖物激活的受体-γ配体用于治疗乳腺癌。

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Pioglitazone and rosiglitazone are thiazolidinediones used for the treatment of Type 2 diabetes mellitus. They modulate glucose and fat metabolism, mainly by binding to the nuclear hormone receptor peroxisome proliferator-activated receptor (PPAR)-gamma. PPAR-gamma signalling is involved in a number of other disease conditions including cancer. In breast cancer cells, PPAR-gamma ligands inhibit proliferation and induce apoptosis both in vitro and in vivo. PPAR-gamma ligands also inhibit tumour angiogenesis and invasion. The only published clinical trial using a PPAR-gamma ligand in patients with metastatic breast cancer failed to show any clinical benefits. The mechanism of action of the thiazolidinediones in breast cancer cells is not fully understood but involves interactions with other nuclear hormone receptors, transcriptional co-activators and repressors as well as PPAR-gamma-independent effects. A better understanding of these mechanisms will be needed before PPAR-gamma ligands may be useful in the treatment of breast cancer patients.
机译:吡格列酮和罗格列酮是用于治疗2型糖尿病的噻唑烷二酮。它们主要通过结合核激素受体过氧化物酶体增殖物激活受体(PPAR)-γ来调节葡萄糖和脂肪的代谢。 PPAR-γ信号转导还涉及许多其他疾病,包括癌症。在乳腺癌细胞中,PPAR-γ配体在体外和体内均抑制增殖并诱导凋亡。 PPAR-γ配体也抑制肿瘤血管生成和侵袭。在转移性乳腺癌患者中使用PPAR-γ配体的唯一公开临床试验未能显示出任何临床益处。噻唑烷二酮在乳腺癌细胞中的作用机理尚未完全了解,但涉及与其他核激素受体,转录共激活因子和阻遏因子的相互作用以及PPAR-γ无关的作用。在PPAR-γ配体可用于治疗乳腺癌患者之前,需要对这些机制有更好的了解。

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