A comparative endpoint study of lesions induced by MoMuSV-m1, MoMuSV-HT1, MoMuSV-124 and MoMuSV-349

R J Hoffman1, G Stoica

  • 1Department of Veterinary Pathology, Oklahoma State University, College of Veterinary Medicine, Stillwater.

Insights

Different Murine Mammary Tumor Virus strains (MoMuSV) induced distinct neoplastic lesions and thymic atrophy in mice. MoMuSV-124 and MoMuSV-349 caused widespread angioproliferative neoplasms, while other strains induced fibrosarcomas or myeloid leukemias.

Area of Science:

  • Oncology
  • Virology
  • Pathology

Background:

  • Murine Mammary Tumor Virus (MoMuSV) strains are known to induce neoplasms in susceptible hosts.
  • Understanding the specific pathological outcomes of different MoMuSV strains is crucial for cancer research.

Purpose of the Study:

  • To compare the clinical, gross, and histologic similarities and differences of neoplasms induced by various MoMuSV strains.
  • To characterize the distinct pathological lesions and thymic atrophy caused by different MoMuSV isolates in BALB/c mice.

Main Methods:

  • Intraperitoneal inoculation of BALB/c mice with different MoMuSV strains (MoMuSV-124, MoMuSV-349, MoMuSV-HT1, MoMuSV-m1).
  • Histological examination of induced neoplasms and organs (thymus, spleen, bone marrow).
  • Clinical and gross pathological assessment of tumor distribution and severity.

Main Results:

  • MoMuSV-124 and MoMuSV-349 induced indistinguishable, widespread angioproliferative neoplasms and severe thymic atrophy.
  • MoMuSV-HT1 induced fibrosarcomas, while MoMuSV-m1 showed features of both angioproliferative neoplasms and fibrosarcomas with less vascularity.
  • MoMuSV-HT1 and MoMuSV-m1 caused thymic atrophy and splenic infiltrates of primitive myeloid cells; MoMuSV-m1 also showed bone marrow involvement suggestive of leukemia.

Conclusions:

  • Different MoMuSV strains induce distinct, predictable histological lesions in BALB/c mice, with MoMuSV-124 and MoMuSV-349 being an exception due to their similarity.
  • The study highlights the strain-specific oncogenic potential of MoMuSV, leading to varied neoplastic types and degrees of thymic atrophy.

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