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Histopathology of hemangiosarcomas in mice and hamsters and liposarcomas/fibrosarcomas in rats associated with PPAR
Jerry F Hardisty1, Michael R Elwell, Heinrich Ernst
1Experimental Pathology Laboratories, Inc. (EDL), Research Triangle Park, NC 27709, USA. jhardisty@epl-inc.com
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.
Insights
Peroxisome proliferator-activated receptors (PPAR) agonists show therapeutic potential for diabetes but can cause rodent tumors. A working group established diagnostic criteria to differentiate these tumors from natural changes.
Area of Science:
- Pharmacology and Toxicology
- Endocrinology
- Oncology
Background:
- Peroxisome proliferator-activated receptors (PPAR) are implicated in insulin resistance and type 2 diabetes.
- PPAR agonists are potential therapeutic targets for diabetes management.
- Rodent studies indicate PPAR agonists may possess tumorigenic potential.
Purpose of the Study:
- To address concerns regarding rodent tumor data associated with PPAR agonists.
- To establish consensus on diagnostic criteria for PPAR agonist-induced tumors in rodents.
- To ensure consistency in tumor diagnosis across multiple studies.
Main Methods:
- Formation of the Health and Environmental Sciences Institute (HESI) PPAR Agonist Project Committee and its Pathology Working Group (PWG).
- Review of rodent carcinogenicity studies focusing on hemangiosarcomas, fibrosarcomas, and liposarcomas.
- Development of standardized morphologic criteria for tumor diagnosis and assessment of preneoplastic changes.
Main Results:
- Consensus on diagnostic criteria for hemangiosarcomas (mice, hamsters) and liposarcomas/fibrosarcomas (rats) was developed.
- Focus on distinguishing treatment-related changes from spontaneous lesions in control animals.
- Recommended specific diagnostic criteria and nomenclature for proliferative vascular and mesenchymal lesions.
Conclusions:
- Standardized diagnostic criteria are crucial for accurately interpreting rodent tumor data from PPAR agonist studies.
- This work aims to improve the understanding of PPAR agonist-induced tumorigenesis and its human relevance.
- Consistent pathological assessment is vital for evaluating the safety and efficacy of PPAR-targeting drugs.

