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

Toxicologic Pathology
|December 22, 2007
PubMed

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.