# Murine cell lines with defined mutations model different histological subtypes of epithelial ovarian cancer

**Authors:** Lixin Zhang, Yusi Fang, Ibrahim Uygun, Danyang Li, Mary Strange, Syed K. Zaidi, Wenjia Wang, Julia Knight, Mackenzy Radolec, Esther Elishaev, Joan F. Brozick, Allison Edwards, George Tseng, Sandra Cascio, Ronald Buckanovich, Robert P. Edwards, Anda M. Vlad

PMC · DOI: 10.1242/dmm.052177 · Disease Models & Mechanisms · 2025-07-28

## TL;DR

Researchers developed mouse cell lines with specific mutations that mimic different types of ovarian cancer, enabling better preclinical studies.

## Contribution

The study introduces a versatile collection of murine cell lines with defined mutations that model various histological subtypes of epithelial ovarian cancer.

## Key findings

- Trp53 null cell lines recapitulate high-grade serous ovarian cancer histology in mice.
- Pten deletion models high-grade endometrioid tumors, while KrasG12D/Pten−/− models carcinosarcoma.
- RNA-sequencing reveals distinct gene expression profiles across different histological models.

## Abstract

Preclinical modeling of epithelial ovarian cancer in immune-competent mice progressing to orthotopic, spontaneous tumors is challenging, requiring multiple genetic modifications in the host. Transplantable models using cell lines are easier to implement than spontaneous animal models, given that they reproduce the key disease characteristics. To create new in vivo ovarian tumor models, we generated 28 murine ovarian cancer cell lines with distinct genetic traits, such as deletion of Trp53, activation of KrasG12D, or deletion of Pten or KrasG12D/Pten−/− combination. Two distinct Trp53 null cell lines recapitulate high-grade serous histology when orthotopically injected into immune-competent, syngeneic hosts. Cells with Pten deletion trigger high-grade endometrioid tumors, and cells with dual KrasG12D activation and Pten deletion model carcinosarcoma. The cells express different tumor antigens, secrete varying levels of cytokines and chemokines, and trigger tumors with diverse inflammation profiles and various intratumoral T- and B-lymphocyte infiltration patterns. RNA-sequencing data from 16 cell lines reveal the gene expression profile across distinct models with different histotypes. This versatile collection of murine cell lines supports translationally relevant studies in ovarian cancer.

Summary: This study provides genotypic and phenotypic analyses of novel murine cell lines that express different antigens and recapitulate in vivo ovarian cancer with different histology and inflammatory profiles.

## Linked entities

- **Genes:** TP53 (tumor protein p53) [NCBI Gene 7157], PTEN (phosphatase and tensin homolog) [NCBI Gene 5728]
- **Diseases:** ovarian cancer (MONDO:0005140), carcinosarcoma (MONDO:0002928)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Pten (phosphatase and tensin homolog) [NCBI Gene 19211] {aka 2310035O07Rik, A130070J02Rik, B430203M17Rik, MMAC1, PTENbeta, TEP1}, Trp53 (transformation related protein 53) [NCBI Gene 22059] {aka Tp53, bbl, bfy, bhy, p44, p53}
- **Diseases:** epithelial ovarian cancer (MESH:D000077216), carcinosarcoma (MESH:D002296), ovarian cancer (MESH:D010051), inflammation (MESH:D007249), tumor (MESH:D009369), endometrioid tumors (MESH:D018269)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12352289/full.md

## References

96 references — full list in the complete paper: https://tomesphere.com/paper/PMC12352289/full.md

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Source: https://tomesphere.com/paper/PMC12352289