The crucial roles of m6A RNA modifications in cutaneous cancers: Implications in pathogenesis, metastasis, drug resistance, and targeted therapies

被引:5
作者
Huang, Cong [1 ]
Zhang, Kaoyuan [2 ]
Guo, Yang [1 ]
Shen, Changbing [2 ]
Liu, Xiaoming [2 ]
Huang, Haiyan [2 ]
Dou, Xia [2 ]
Yu, Bo [1 ]
机构
[1] Hong Kong Univ Sci & Technol, Peking Univ Shenzhen Hosp, Shenzhen Peking Univ, Dept Dermatol,Skin Res Inst,Med Ctr, Shenzhen 518036, Guangdong, Peoples R China
[2] Peking Univ Shenzhen Hosp, Skin Res Inst, Dept Dermatol, Shenzhen 518036, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Cutaneous squamous cell carcinoma; Cutaneous melanoma; m6A modification; m6A-related drugs; Target Therapy; SQUAMOUS-CELL CARCINOMA; MECLOFENAMIC ACID; DEMETHYLASE FTO; N-6-METHYLADENOSINE M(6)A; CRYSTAL-STRUCTURES; IMPROVED SURVIVAL; BINDING-PROTEIN; MEK INHIBITION; SELF-RENEWAL; RISK-FACTORS;
D O I
10.1016/j.gendis.2022.03.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
N6-methyladenosine (m6A) is the most abundant internal modification on RNA. It is a dynamical and reversible process, which is regulated by m6A methyltransferase and m6A demethylase. The m6A modified RNA can be specifically recognized by the m6A reader, leading to RNA splicing, maturation, degradation or translation. The abnormality of m6A RNA modification is closely related to a variety of biological processes, especially the occurrence and development of tumors. Recent studies have shown that m6A RNA modification is involved in the pathogenesis of skin cancers. However, the precise molecular mechanisms of m6A-mediated cutaneous tumorigenesis have not been fully elucidated. Therefore, this review will summarize the biological characteristics of m6A modification, its regulatory role and mechanism in skin cancers, and the recent research progress of m6A-related molecular drugs, aiming to provide new ideas for clinical diagnosis and targeted therapy of cutaneous cancers.& COPY; 2022 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons. org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:2320 / 2330
页数:11
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