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Article

Chidamide suppresses the glycolysis of triple negative breast cancer cells partially by targeting the miR‑33a‑5p‑LDHA axis

  • Authors:
    • Xiangdong Bai
    • Hongchuan Jiang
    • Guohui Han
    • Qiang He
  • View Affiliations / Copyright

    Affiliations: Department of Breast Surgery, Shanxi Provincial Cancer Hospital, Shanxi Medical University, Taiyuan, Shanxi 030013, P.R. China, Department of Breast Surgery, Beijing Chaoyang Hospital, The Affiliated Hospital of Capital Medical University, Beijing 100020, P.R. China, Department of Hepatobiliary Surgery, Beijing Chaoyang Hospital, The Affiliated Hospital of Capital Medical University, Beijing 100020, P.R. China
  • Pages: 1857-1865
    |
    Published online on: June 25, 2019
       https://doi.org/10.3892/mmr.2019.10425
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Abstract

Triple negative breast cancer (TNBC) is one of the most aggressive types of breast cancer and has a poor prognosis. Therefore, the development of novel drugs and understanding the molecular mechanisms that may contribute to the initiation and development of TNBC are urgently required. Chidamide, a histone deacetylase inhibitor, has been reported as possessing anti‑cancer properties in several cancers, however, the function of chidamide in TNBC remains to be elucidated. The present study revealed that chidamide inhibited the proliferation, colony formation and migration of TNBC cells. Experiments investigating the underlying mechanism revealed that chidamide upregulated the expression of microRNA (miR)‑33a‑5p in TNBC cells via RT‑qPCR. Luciferase reporter assay demonstrated that miR‑33a‑5p was bound to the 3'‑untranslated region of lactate dehydrogenase A (LDHA) and decreased the expression of LDHA in TNBC cells. In addition, chidamide suppressed the expression of LDHA and significantly decreased the glycolysis of TNBC cells. Collectively, the results of the present study demonstrated that chidamide reprogramed glucose metabolism, partially by targeting the miR‑33a‑5p/LDHA pathway, in TNBC. These findings indicate that chidamide may be a promising novel drug in the treatment of patients with TNBC.
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Copy and paste a formatted citation
Spandidos Publications style
Bai X, Jiang H, Han G and He Q: Chidamide suppresses the glycolysis of triple negative breast cancer cells partially by targeting the miR‑33a‑5p‑LDHA axis. Mol Med Rep 20: 1857-1865, 2019.
APA
Bai, X., Jiang, H., Han, G., & He, Q. (2019). Chidamide suppresses the glycolysis of triple negative breast cancer cells partially by targeting the miR‑33a‑5p‑LDHA axis. Molecular Medicine Reports, 20, 1857-1865. https://doi.org/10.3892/mmr.2019.10425
MLA
Bai, X., Jiang, H., Han, G., He, Q."Chidamide suppresses the glycolysis of triple negative breast cancer cells partially by targeting the miR‑33a‑5p‑LDHA axis". Molecular Medicine Reports 20.2 (2019): 1857-1865.
Chicago
Bai, X., Jiang, H., Han, G., He, Q."Chidamide suppresses the glycolysis of triple negative breast cancer cells partially by targeting the miR‑33a‑5p‑LDHA axis". Molecular Medicine Reports 20, no. 2 (2019): 1857-1865. https://doi.org/10.3892/mmr.2019.10425
Copy and paste a formatted citation
x
Spandidos Publications style
Bai X, Jiang H, Han G and He Q: Chidamide suppresses the glycolysis of triple negative breast cancer cells partially by targeting the miR‑33a‑5p‑LDHA axis. Mol Med Rep 20: 1857-1865, 2019.
APA
Bai, X., Jiang, H., Han, G., & He, Q. (2019). Chidamide suppresses the glycolysis of triple negative breast cancer cells partially by targeting the miR‑33a‑5p‑LDHA axis. Molecular Medicine Reports, 20, 1857-1865. https://doi.org/10.3892/mmr.2019.10425
MLA
Bai, X., Jiang, H., Han, G., He, Q."Chidamide suppresses the glycolysis of triple negative breast cancer cells partially by targeting the miR‑33a‑5p‑LDHA axis". Molecular Medicine Reports 20.2 (2019): 1857-1865.
Chicago
Bai, X., Jiang, H., Han, G., He, Q."Chidamide suppresses the glycolysis of triple negative breast cancer cells partially by targeting the miR‑33a‑5p‑LDHA axis". Molecular Medicine Reports 20, no. 2 (2019): 1857-1865. https://doi.org/10.3892/mmr.2019.10425
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