# CMLPS-N1: a novel preclinical cell line model for canine mammary tumor and its application in therapeutic screening

**Authors:** Xiao Wang, Han Zhou, Qian Zhang, Yihan Liu, Lixin He, Wenxuan Li, Bin Ma, Lihong Luo, Lijun Guo, Changwei Qiu

PMC · DOI: 10.1080/01652176.2026.2614697 · The Veterinary Quarterly · 2026-01-10

## TL;DR

A new canine mammary liposarcoma cell line, CMLPS-N1, was developed to study aggressive tumors and test potential therapies in dogs.

## Contribution

The first preclinical cell line derived from a spontaneous canine mammary liposarcoma, enabling therapeutic screening.

## Key findings

- CMLPS-N1 exhibits high proliferative, migratory, and tumorigenic properties consistent with liposarcoma.
- The cell line expresses high-risk markers and lacks epithelial and HER-2 markers, confirming its aggressive mesenchymal phenotype.
- Cytotoxicity testing with chemotherapy agents supports its use as a model for therapeutic screening.

## Abstract

Canine mammary tumor is the most common tumor in intact female dogs and poses a growing health burden due to its high malignancy rate and increasing canine populations. However, research on sarcomatous subtypes has been hindered by a lack of representative cell lines. Here, we successfully established a novel canine mammary liposarcoma cell line, designated CMLPS-N1, which represents the first such model derived from a spontaneous tumor. This cell line has been stably maintained for over 80 passages and exhibits an abnormal karyotype, high proliferative and migratory capacity, and strong tumorigenicity in mouse xenografts. Molecular profiling confirmed a phenotype consistent with liposarcoma (MDM2+) and mesenchymal origin (Vimentin+/N-cadherin+), alongside high-risk markers (p53+/Ki67+/Notch1), and hormone receptor expression (ER/PR), while being negative for epithelial (PCK) and HER-2 markers. We used functional assays, including cell proliferation, colony formation, wound healing, and transwell invasion, to confirm its aggressive phenotype. Furthermore, cytotoxicity testing with four chemotherapy agents further supports its utility as a preclinical model for therapeutic screening and mechanistic research. The establishment of CMLPS-N1 enriches the canine mammary tumor cell line repository and provides a valuable experimental model for studying disease mechanisms, developing therapies, and facilitating translational applications.

## Linked entities

- **Genes:** MDM2 (MDM2 proto-oncogene) [NCBI Gene 4193], PRELID1 (PRELI domain containing 1) [NCBI Gene 737446], CadN (Cadherin-N) [NCBI Gene 35070], TP53 (tumor protein p53) [NCBI Gene 7157], Mki67 (antigen identified by monoclonal antibody Ki 67) [NCBI Gene 17345], NOTCH1 (notch receptor 1) [NCBI Gene 4851], EREG (epiregulin) [NCBI Gene 2069], PGR (progesterone receptor) [NCBI Gene 5241], pck (pickel) [NCBI Gene 31101], ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064]
- **Diseases:** liposarcoma (MONDO:0003585)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** VIM (vimentin) [NCBI Gene 477991], TP53 (tumor protein p53) [NCBI Gene 403869] {aka P53}, MDM2 (MDM2 proto-oncogene) [NCBI Gene 403693], NOTCH1 (notch receptor 1) [NCBI Gene 480676] {aka N1ICD}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 403883] {aka HER-2, c-erbB-2, p185erbB2}
- **Diseases:** malignancy (MESH:D009369), sarcomatous (MESH:D018316), mammary tumor (MESH:D015674), liposarcoma (MESH:D008080), cytotoxicity (MESH:D064420)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Canis lupus familiaris (dog, subspecies) [taxon 9615]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12794710/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12794710/full.md

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Source: https://tomesphere.com/paper/PMC12794710