Alternative mouse models for carcinogenicity assessment: industry use and issues with pathology interpretation

Gerald G Long1, Daniel Morton, Terry Peters

  • 1Lilly Research Laboratories, Indianapolis, Indiana 46225, USA. Long_gerald_g@lilly.com

Toxicologic Pathology
|November 17, 2009
PubMed

Insights

The Carcinogenicity Alternative Mouse Models (CAMM) survey shows these models are increasingly accepted by regulatory agencies to replace traditional long-term mouse bioassays. Key challenges include data interpretation and study conduct, with recommendations for standardization.

Area of Science:

  • Toxicologic Pathology
  • Genetically Modified Mouse Models
  • Carcinogenicity Testing

Background:

  • Industry practices and opinions on alternative mouse models for carcinogenicity testing were surveyed.
  • The Carcinogenicity Alternative Mouse Models (CAMM) Working Group of the Society of Toxicologic Pathology (STP) conducted the survey.

Purpose of the Study:

  • To define current industry practices and opinions on using alternative mouse models for carcinogenicity testing.
  • To identify challenges and develop recommendations for the implementation and interpretation of these models.

Main Methods:

  • A survey was distributed to members of the Society of Toxicologic Pathology.
  • Results were analyzed to identify common practices, regulatory acceptance, and challenges associated with CAMM.

Main Results:

  • CAMM are primarily used to meet regulatory requirements, replacing the two-year mouse bioassay and gaining regulatory acceptance.
  • The p53+/- and rasH2 models are most common, with rasH2 being widely accepted for general carcinogenicity testing.
  • Challenges include lack of historical data, unexpected tumor findings, pathology evaluation, animal numbers, survival, and study duration.

Conclusions:

  • CAMM are a viable alternative to traditional carcinogenicity testing, with growing regulatory acceptance.
  • Recommendations focus on standardizing positive control testing, histopathologic examination, diagnostic criteria, and historical data utilization.
  • Further development and use of genetically modified mice in carcinogenicity testing are encouraged.

Related Concept Videos

Mouse Models of Cancer Study02:43

Mouse Models of Cancer Study

Mice have long served as models for studying human biology and pathology because of their phylogenetic and physiological similarity with humans. They are also easy to maintain and breed in the laboratory, and hence, many inbred strains are now available for research. Studies on mice have contributed immeasurably to our understanding of cancer biology.
The development of transgenic, knockout, and knock-in mice has led to an exponential increase in their use as model organisms in research,...
Mouse Models of Cancer Study02:43

Mouse Models of Cancer Study

Mice have long served as models for studying human biology and pathology because of their phylogenetic and physiological similarity with humans. They are also easy to maintain and breed in the laboratory, and hence, many inbred strains are now available for research. Studies on mice have contributed immeasurably to our understanding of cancer biology.
The development of transgenic, knockout, and knock-in mice has led to an exponential increase in their use as model organisms in research,...
Mutagenicity and Carcinogenicity01:25

Mutagenicity and Carcinogenicity

Mutagenicity and carcinogenicity refer to the ability of drugs to cause genetic defects and induce cancer, respectively. The International Agency for Research on Cancer (IARC) classifies agents into four groups based on their carcinogenic potential. Group 1 agents are known human carcinogens; group 2A agents are probably carcinogenic to humans; group 3 agents lack data to support their role in carcinogenesis; and group 4 includes agents for which data support that they are not likely to be...