Novel organoid-based exploration reveals the role of LMTK3/FADS2 signaling in metastatic breast cancer progression in felines and humans

Cancer research in veterinary medicine is still under development compared to human medicine. Feline breast cancer (FBC) is highly malignant, intractable, and has the potential to become a valuable model for human metastatic BC (HBC). We developed primary FBC organoids and analyzed their morphology, gene expression patterns, and response to anti-cancer drugs. FBC organoids recapitulated the structure and behavior of tumor cells, exhibiting diverse hormone receptor expressions and tumorigenic potential. Moreover, varying sensitivities to chemotherapies and targeted drugs were evident across FBC organoid lines. Furthermore, LMTK3 was significantly upregulated in FBC organoids compared to feline normal mammary organoids (FNM). Further, LMTK3/FADS2 pathway was revealed to be implicated in progression by influencing cell proliferation, invasion, and apoptosis of FBC organoids. Treatment with C28 (an LMTK3 inhibitor) also prevented cell viability of human BC organoids. The survival time of human BC patients with high co-expression of LMTK3 and FADS2 was shorter than that with low co-expression. These findings highlight the importance of LMTK3/FADS2 pathway in BC progression and indicate that FBC organoids might help to do comparative research and identify conserved mechanisms between HBC and FBC.

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Publication Details

Journal
Scientific Reports
Published
2025-11-22
DOI
https://doi.org/10.1038/s41598-025-28751-7
Primary Topic
Veterinary Oncology Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Novel organoid-based exploration reveals the role of LMTK3/FADS2 signaling in metastatic breast cancer progression in felines and humans

Yusuke Ishihara, Hideyuki Yamawaki, Yuko Nagashima, Daigo Azakami et al.
Scientific Reports
Veterinary Oncology Research
article

Novel organoid-based exploration reveals the role of LMTK3/FADS2 signaling in metastatic breast cancer progression in felines and humans

Yusuke Ishihara, Hideyuki Yamawaki, Yuko Nagashima, Daigo Azakami, Ryouichi Tsunedomi, Mohamed Elbadawy, Tsuyoshi Uchide, Toshinori Yoshida, Makoto Shibutani, Yuki Kobayashi, Tatsuya Usui, R Matsui, Suzuka Uomoto, Ting-Wei Yu, Masahiro Kaneda, Amira Abugomaa, Masaki Inoue, Yishan Liu, Ryuji Fukushima, Tetsuya J. Kobayashi, Yomogi Shiota, Yuta Shinohara, Haru Yamamoto, Mio Kobayashi, Kazuaki SASAKI, Noriko Maeda, Midori Higashinaka
article en

Abstract

Cancer research in veterinary medicine is still under development compared to human medicine. Feline breast cancer (FBC) is highly malignant, intractable, and has the potential to become a valuable model for human metastatic BC (HBC). We developed primary FBC organoids and analyzed their morphology, gene expression patterns, and response to anti-cancer drugs. FBC organoids recapitulated the structure and behavior of tumor cells, exhibiting diverse hormone receptor expressions and tumorigenic potential. Moreover, varying sensitivities to chemotherapies and targeted drugs were evident across FBC organoid lines. Furthermore, LMTK3 was significantly upregulated in FBC organoids compared to feline normal mammary organoids (FNM). Further, LMTK3/FADS2 pathway was revealed to be implicated in progression by influencing cell proliferation, invasion, and apoptosis of FBC organoids. Treatment with C28 (an LMTK3 inhibitor) also prevented cell viability of human BC organoids. The survival time of human BC patients with high co-expression of LMTK3 and FADS2 was shorter than that with low co-expression. These findings highlight the importance of LMTK3/FADS2 pathway in BC progression and indicate that FBC organoids might help to do comparative research and identify conserved mechanisms between HBC and FBC.

Scientific ReportsVol. 15(1)
Canon (Japan) (JP), Mansoura University (EG), Yamaguchi University (JP), Benha University (EG), Yamaguchi University Hospital (JP), Japan Small Animal Medical Center (JP), Himeji Medical Center (JP), Ajinomoto (Japan) (JP), Kitasato University (JP), Tokyo University of Agriculture and Technology (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 49%
Veterinary Oncology Research
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