Related Experiment Video
Updated: Nov 2, 2025

08:12
The Use of Mouse Mammary Tumor Cells in an In Vitro Invasion Assay as a Measure of Oncogenic Cell Behavior
Published on: June 12, 2019
5.3K
A Novel Canine Mammary Cancer Cell Line: Preliminary Identification and Utilization for Drug Screening Studies
Rifei Li1, Haoxian Wu1, Yue Sun1
1College of Veterinary Medicine, China Agricultural University, Beijing, China.
Frontiers in Veterinary Science
|June 14, 2021
Summary
A new canine mammary cancer cell line, B-CMT, was developed for studying fatal neoplastic diseases in dogs. This model showed promise for screening therapeutic drugs, with rapamycin and imatinib inhibiting cancer cell proliferation.
Area of Science:
- Veterinary Oncology
- Cancer Cell Line Development
- Comparative Pathology
Background:
- Canine malignant mammary tumors are aggressive and have a poor prognosis.
- There is a need for reliable cell models to study canine mammary cancer and test potential therapies.
Purpose of the Study:
- To establish and characterize a novel canine mammary cancer cell line (B-CMT).
- To utilize B-CMT as an in vitro model for screening therapeutic drugs against canine mammary tumors.
Main Methods:
- Establishment and long-term culture of the B-CMT cell line.
- Characterization using qRT-PCR, immunofluorescence, western blot, and immunohistochemistry.
- In vivo studies in mice to confirm tumor formation from B-CMT cells.
- In vitro drug cytotoxicity assays.
Main Results:
- B-CMT cells exhibited rapid proliferation with a population doubling time of 33.6 hours.
- The cell line lacked expression of HER-2, ER, and PR, but showed decreased CDH1 and increased GATA3.
- Positive expression of hypoxia-inducible factor-1α (HIF-1α) was observed.
- Rapamycin and imatinib demonstrated significant in vitro cytotoxicity and induced cell cycle arrest.
Conclusions:
- The B-CMT cell line is a viable model for canine mammary cancer research.
- This cell line can be used for in vitro drug screening and studying tumor microenvironment and drug resistance.

