Suppr超能文献

与过氧化物酶体增殖物激活受体(PPAR)激动剂相关的小鼠血管肉瘤、仓鼠血管肉瘤以及大鼠脂肪肉瘤/纤维肉瘤的组织病理学

Histopathology of hemangiosarcomas in mice and hamsters and liposarcomas/fibrosarcomas in rats associated with PPAR agonists.

作者信息

Hardisty Jerry F, Elwell Michael R, Ernst Heinrich, Greaves Peter, Kolenda-Roberts Holly, Malarkey David E, Mann Peter C, Tellier Pierre A

机构信息

Experimental Pathology Laboratories, Inc. (EDL), Research Triangle Park, NC 27709, USA.

出版信息

Toxicol Pathol. 2007 Dec;35(7):928-41. doi: 10.1080/01926230701748156.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e7b4/2366205/dba3cbfb4887/nihms-44578-f0001.jpg

相似文献

4
Evolution of peroxisome proliferator-activated receptor agonists.过氧化物酶体增殖物激活受体激动剂的演变
Ann Pharmacother. 2007 Jun;41(6):973-83. doi: 10.1345/aph.1K013. Epub 2007 May 22.
7
Effects of the PPARgamma agonist troglitazone on endothelial cells in vivo and in vitro: differences between human and mouse.
Toxicol Appl Pharmacol. 2009 May 15;237(1):83-90. doi: 10.1016/j.taap.2009.02.028. Epub 2009 Mar 11.

引用本文的文献

2
Angiomatous hyperplasia in the heart of a young rat.幼鼠心脏中的血管瘤样增生。
J Toxicol Pathol. 2020 Jan;33(1):29-32. doi: 10.1293/tox.2019-0059. Epub 2019 Dec 5.
5
Metastatic hemangiosarcoma of the liver in a young rat.一只幼鼠肝脏的转移性血管肉瘤
J Toxicol Pathol. 2017 Jan;30(1):75-78. doi: 10.1293/tox.2016-0040. Epub 2016 Oct 31.
7
Proceedings of the 2014 National Toxicology Program Satellite Symposium.2014年国家毒理学计划卫星研讨会会议记录
Toxicol Pathol. 2015 Jan;43(1):10-40. doi: 10.1177/0192623314555526. Epub 2014 Nov 9.

本文引用的文献

1
Thiazolidinediones.噻唑烷二酮类
N Engl J Med. 2004 Sep 9;351(11):1106-18. doi: 10.1056/NEJMra041001.
5
Rodent carcinogenicity with the thiazolidinedione antidiabetic agent troglitazone.
Toxicol Sci. 2002 Jul;68(1):226-36. doi: 10.1093/toxsci/68.1.226.
6
Spontaneous and thiazolidinedione-induced B6C3F1 mouse hemangiosarcomas exhibit low ras oncogene mutation frequencies.
Toxicol Appl Pharmacol. 1999 Oct 15;160(2):133-40. doi: 10.1006/taap.1999.8763.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验