Hardisty Jerry F, Elwell Michael R, Ernst Heinrich, Greaves Peter, Kolenda-Roberts Holly, Malarkey David E, Mann Peter C, Tellier Pierre A
Experimental Pathology Laboratories, Inc. (EDL), Research Triangle Park, NC 27709, USA.
Toxicol Pathol. 2007 Dec;35(7):928-41. doi: 10.1080/01926230701748156.
Peroxisome proliferator-activated receptors (PPAR) are involved in the pathogenesis of insulin resistance, diabetes, and related complications. Consequently, the identification of PPAR subtypes and the potential for their activation provides promising therapeutic targets for the management of type 2 diabetes mellitus. Available data from rodent carcinogenicity studies, however, demonstrate that PPAR agonists can be tumorigenic in one or more species of rodents at multiple sites. In 2005, the Health and Environmental Sciences Institute (HESI) PPAR Agonist Project Committee was established by a group of pharmaceutical companies to advance research on and to understand the modes of action and human relevance of this emerging rodent tumor data for PPAR agonists. Since the most commonly observed tumor types reported in rodents are hemangiosarcomas, fibrosarcomas and liposarcomas, the PPAR Agonist Project Committee approved a Pathology Working Group (PWG) to develop consensus of morphologic criteria for tumor diagnoses and consistency of diagnoses across multiple studies for hemangiosarcomas in mice and hamsters and liposarcomas/fibrosarcomas in rats. Therefore, the focus of the PWG review was to establish consistent tumor diagnostic criteria, to assess evidence of potentially preneoplastic changes and to identify distinguishing morphologic differences which may exist between spontaneous changes present in control animals with similar changes from treated animals. Specific diagnostic criteria and nomenclature are recommended for the classification of proliferative vascular lesions which may be present in mice or hamsters and for proliferative mesenchymal changes in rats in studies that are conducted with PPAR agonists.
过氧化物酶体增殖物激活受体(PPAR)参与胰岛素抵抗、糖尿病及相关并发症的发病机制。因此,鉴定PPAR亚型及其激活潜力为2型糖尿病的治疗提供了有前景的治疗靶点。然而,来自啮齿动物致癌性研究的现有数据表明,PPAR激动剂在多种啮齿动物的一个或多个部位可致瘤。2005年,一组制药公司成立了健康与环境科学研究所(HESI)PPAR激动剂项目委员会,以推进对这一新兴的PPAR激动剂啮齿动物肿瘤数据的作用模式和与人类相关性的研究并加深理解。由于啮齿动物中最常观察到的肿瘤类型是血管肉瘤、纤维肉瘤和脂肪肉瘤,PPAR激动剂项目委员会批准了一个病理学工作组(PWG),以就小鼠和仓鼠血管肉瘤以及大鼠脂肪肉瘤/纤维肉瘤的肿瘤诊断形态学标准和多项研究诊断的一致性达成共识。因此,PWG审查的重点是建立一致的肿瘤诊断标准,评估潜在癌前病变的证据,并识别对照动物中存在的自发变化与处理动物中类似变化之间可能存在的形态学差异。对于使用PPAR激动剂进行的研究中可能存在于小鼠或仓鼠的增殖性血管病变以及大鼠的增殖性间充质变化的分类,建议采用特定的诊断标准和命名法。