1.1)Institute of Immunology and Molecular Medicine, Jining Medical University, Jining 272067, China;2.2)State Key Laboratory of Medicinal Chemical Biology, Department of Biochemistry, College of Life Sciences, Nankai University, Tianjin 300071, China;3.3)School of Life Sciences, Liaoning University, Shenyang 110036, China
This work was supported by grants from The National Natural Science Foundation of China(81802856, 31800688), The Projects of Shandong Province Higher Education Science and Technology (J17KA230), The Shandong Province Undergraduate Training Program for Innovation and Entrepreneurship (201910443011) and The National Level of Local Universities Undergraduate Training Program for Innovation and Entrepreneurship (201610443043).
Breast cancer is the most common cancer and the leading cause of cancer death in women worldwide. Although huge progress has been made in managing early-stage breast cancer, no effective strategy can prevent or treat breast cancer metastasis which has high recurrence rate and high mortality rate. Thus, identification of new molecular markers for the diagnosis and prognostic prediction of metastatic breast cancer and development of innovative therapeutic measures are urgently needed. Recently, epigenetic regulation of the expression and function of oncogenes by aberrant N6-methyladenosine (m6A) modification of mRNA in aggressive breast cancer is investigated widely. In this review, we retrieve and analyze the most recent studies on m6A modification, and summarize the expression and the function of m6A regulatory proteins, including the writers, erasers and readers, in the tumorigenesis and progression of breast cancer, and point out the defects in the recent field of m6A-related researches, so as to provide scientific basis for diagnosis, therapies and prognosis in breast cancer.
FANG Run-Ping, XU Fei-Fei, ZHAO Lu-Ping, YU Lu, CAI Xiao-Li, YANG Zhe, ZHANG Wei-Ying, YE Li-Hong, SHI Hui. The Roles of m6A Modification in Breast Cancer[J]. Progress in Biochemistry and Biophysics,2021,48(5):550-559
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