Pronecroptotic Therapy Using Ceramide Nanoliposomes Is Effective for Triple-Negative Breast Cancer Cells

Author:

Ohya Yuki1,Ogiso Yuri1,Matsuda Masaya1ORCID,Sakae Harumi1,Nishida Kentaro1,Miki Yasuhiro2ORCID,Fox Todd E.3ORCID,Kester Mark3,Sakamoto Wataru4,Nabe Takeshi1,Kitatani Kazuyuki1ORCID

Affiliation:

1. Faculty of Pharmaceutical Sciences, Setsunan University, Hirakata 573-0101, Japan

2. Department of Pathology, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan

3. Department of Pharmacology, University of Virginia, Charlottesville, VA 22908-8735, USA

4. Research Center of Oncology, Ono Pharmaceutical, Co., Ltd., Osaka 618-8585, Japan

Abstract

Regulated necrosis, termed necroptosis, represents a potential therapeutic target for refractory cancer. Ceramide nanoliposomes (CNLs), considered potential chemotherapeutic agents, induce necroptosis by targeting the activating protein mixed lineage kinase domain-like protein (MLKL). In the present study, we examined the potential of pronecroptotic therapy using CNLs for refractory triple-negative breast cancer (TNBC), for which there is a lack of definite and effective therapeutic targets among the various immunohistological subtypes of breast cancer. MLKL mRNA expression in tumor tissues was significantly higher in TNBC patients than in those with non-TNBC subtypes. Similarly, among the 50 breast cancer cell lines examined, MLKL expression was higher in TNBC-classified cell lines. TNBC cell lines were more susceptible to the therapeutic effects of CNLs than the non-TNBC subtypes of breast cancer cell lines. In TNBC-classified MDA-MB-231 cells, the knockdown of MLKL suppressed cell death induced by CNLs or the active substance short-chain C6-ceramide. Accordingly, TNBC cells were prone to CNL-evoked necroptotic cell death. These results will contribute to the development of CNL-based pronecroptotic therapy for TNBC.

Funder

Japan Society for the Promotion of Science

Publisher

MDPI AG

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Bioactive sphingolipids as emerging targets for signal transduction in cancer development;Biochimica et Biophysica Acta (BBA) - Reviews on Cancer;2024-09

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