Ursolic Acid Enhances Cytotoxicity of Doxorubicin-Resistant Triple-Negative Breast Cancer Cells via ZEB1-AS1 /miR-186-5p/ ABCC1 Axis

• Published in: Cancer biotherapy & radiopharmaceuticals Vol. 37; no. 8; p. 673
• Main Authors: Lu, Qing, Chen, Weili, Ji, Yajie, Liu, Yu, Xue, Xiaohong
• Format: Journal Article
• Language: English
• Published: United States 01-10-2022
• Subjects: Cell Line, Tumor; Cell Proliferation - genetics; Doxorubicin - pharmacology; Female; Gene Expression Regulation, Neoplastic; Humans; MicroRNAs - metabolism; Paclitaxel - pharmacology; RNA, Long Noncoding - genetics; Triple Negative Breast Neoplasms - drug therapy; Triple Negative Breast Neoplasms - genetics; Triterpenes - pharmacology; Ursolic Acid; Zinc Finger E-box-Binding Homeobox 1 - genetics; Zinc Finger E-box-Binding Homeobox 1 - metabolism; ABCC1; triple-negative breast cancer; ZEB1-AS1; doxorubicin resistance; ursolic acid
• ISSN: 1557-8852
• DOI: 10.1089/cbr.2020.4147

Triple-negative breast cancer (TNBC) is the most serious subtype of breast cancer (BC) and has been a great health threat to females. Although chemotherapeutic agent contributes a lot to TNBC treatment, drug resistance has been a great obstacle for chemotherapies. Ursolic acid (UA), a pentacyclic triterpenoid compound, was reported to reverse paclitaxel resistance in BC. However, whether UA could affect the resistance of TNBC cells to other drugs such as doxorubicin (DOX) remains to be discovered.
MTT assay, EdU assay, colony formation assay, and flow cytometry analysis were implemented to detect the viability, proliferation, and apoptosis of DOX-resistant MDA-MB-468 and MDA-MB-436 cells with or without UA treatment. Mechanism assays including RIP, RNA pull-down, and luciferase reporter assays verified the interaction between RNAs.
UA treatment hindered the growth and mitigated the DOX resistance of DOX-resistant MDA-MB-468 and MDA-MB-436 cells. Mechanistically, multidrug resistance-associated protein 1 (
) expression was downregulated by UA treatment. MiR-186-5p was verified to target
. Further, UA-inhibited
(zinc finger E-box binding homeobox 1 antisense RNA 1) was verified as a competitive endogenous RNA (ceRNA) to upregulate
through sponging miR-186-5p. Importantly, UA treatment impaired the malignant phenotypes of DOX-resistant MDA-MB-468 and MDA-MB-436 cells through
axis.
UA promotes TNBC cell sensitivity to DOX through inactivating
miR-186-5p
signaling.