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Potential of Peroxisome Proliferator-Activated Receptor Gamma Antagonist Compounds as Therapeutic Agents for a Wide Range of Cancer Types

机译:过氧化物酶体增殖物激活的受体γ拮抗剂化合物作为多种癌症类型的治疗剂的潜力

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摘要

PPARγ is a therapeutic target that has been exploited for treatment of type II diabetes mellitus (T2DM) with agonist drugs. Since PPARγ is expressed by many hematopoietic, mesodermal and epithelial cancers, agonist drugs were tested and shown to have both preclinical and clinical anticancer activities. While preclinical activity has been observed in many cancer types, clinical activity has been observed only in pilot and phase II trials in liposarcoma and prostate cancer. Most studies address agonist compounds, with substantially fewer reports on anticancer effects of PPARγ antagonists. In cancer model systems, some effects of PPARγ agonists were not inhibited by PPARγ antagonists, suggesting noncanonical or PPARγ-independent mechanisms. In addition, PPARγ antagonists, such as T0070907 and GW9662, have exhibited antiproliferative effects on a broad range of hematopoietic and epithelial cell lines, usually with greater potency than agonists. Also, additive antiproliferative effects of combinations of agonist plus antagonist drugs were observed.Finally, there are preclinical in vivo data showing thatantagonist compounds can be administered safely, with favorablemetabolic effects as well as antitumor effects. Since PPARγantagonists represent a new drug class that holds promise as abroadly applicable therapeutic approach for cancer treatment, itis the subject of this review.
机译:PPARγ是已经被开发用于用激动剂药物治疗II型糖尿病(T2DM)的治疗靶标。由于PPARγ在许多造血,中胚层和上皮癌中都有表达,因此对激动剂进行了测试,并显示出具有临床前和临床抗癌活性。尽管在许多癌症类型中均已观察到临床前活性,但仅在脂肪肉瘤和前列腺癌的中试和II期试验中才观察到临床活性。大多数研究都针对激动剂化合物,而有关PPARγ拮抗剂的抗癌作用的报道却很少。在癌症模型系统中,PPARγ激动剂的某些作用并未被PPARγ拮抗剂抑制,这表明非典型或非PPARγ依赖性机制。另外,PPARγ拮抗剂,例如T0070907和GW9662,已对多种造血细胞和上皮细胞系表现出抗增殖作用,通常具有比激动剂更大的效力。另外,观察到激动剂与拮抗剂药物组合的加性抗增殖作用。最后,临床前体内数据表明拮抗剂化合物可以安全地服用代谢作用以及抗肿瘤作用。由于PPARγ拮抗剂代表了一种有希望作为一种新药广泛适用于癌症治疗的治疗方法是此评论的主题。

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