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Thioridazine combined with carboplatin results in synergistic inhibition of triple negative breast cancer by targeting cancer stem cells

Yi Wang, Leiming Xia, Jing Lin, Gong Li, Xia Yang, Yang Xu, Liu Liu, Jianqiang Bao, Congshu Zhang, Yuqing Chai, Hongxia Li

2022Translational Oncology16 citationsDOIOpen Access PDF

Abstract

Cancer stem cells (CSCs) in triple-negative breast cancer (TNBC) are closely related to tumorigenesis and metastasis. Thioridazine (THZ) is a usual phenothiazine antipsychotic drug that can destroy CSCs. We aimed to explore whether THZ could sensitize metastatic TNBC cells, especially the CSCs, to carboplatin (CBP) treatment. Metastatic TNBC cells, 4T1 cells, and tumor-bearing mice were treated with THZ and CBP as monotherapy or combination therapy. MTT, flow cytometry, electron microscopy, immunohistochemistry and western blotting were applied to assess the cell viability, apoptosis, mitochondrial morphology and the relevant protein levels, respectively. Tumor size and lung metastasis under different treatments as well as tumorigenesis of residual tumor cells from each group were monitored. THZ combined with CBP inhibited 4T1 tumor cell proliferation and induced apoptosis by inhibiting the PI3K-AKT-mTOR pathway and activating estrogen receptor stress. THZ also showed strong activity against breast CSCs, THZ combined with CBP significantly destroyed cancer cells, inhibited lung metastasis and relieved the tumor burden; Our data demonstrated that THZ can sensitize TNBC cells to CBP treatment and this combination therapy may provide a bright strategy for TNBC treatment by targeting both cancer cells and CSCs.

Topics & Concepts

Triple-negative breast cancerCancer researchCarboplatinCarcinogenesisCancer stem cellMetastasisCancerBreast cancerPI3K/AKT/mTOR pathwayMedicineCancer cellApoptosisChemistryInternal medicineChemotherapyCisplatinBiochemistryCancer therapeutics and mechanismsPhenothiazines and Benzothiazines Synthesis and ActivitiesCancer Cells and Metastasis