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m6A去甲基化酶FTO与骨质疏松症:潜在的治疗干预措施

m6A demethylase FTO and osteoporosis: potential therapeutic interventions.

作者信息

Huang Mei, Guo Jianmin, Liu Lifei, Jin Haiming, Chen Xi, Zou Jun

机构信息

School of Kinesiology, Shanghai University of Sport, Shanghai, China.

Department of Rehabilitation, The People's Hospital of Liaoning Province, Shenyang, China.

出版信息

Front Cell Dev Biol. 2023 Nov 10;11:1275475. doi: 10.3389/fcell.2023.1275475. eCollection 2023.

Abstract

Osteoporosis is a common bone disease, characterized by a descent in bone mass due to the dysregulation of bone homeostasis. Although different studies have identified an association between osteoporosis and epigenetic alterations in osteogenic genes, the mechanisms of osteoporosis remain unclear. N6-methyladenosine (m6A) modification is a methylated adenosine nucleotide, which regulates the translocation, exporting, translation, and decay of RNA. FTO is the first identified m6A demethylase, which eliminates m6A modifications from RNAs. Variation in disturbs m6A methylation in RNAs to regulate cell proliferation, differentiation, and apoptosis. Besides, FTO as an obesity-associated gene, also affects osteogenesis by regulating adipogenesis. Pharmacological inhibition of FTO markedly altered bone mass, bone mineral density and the distribution of adipose tissue. Small molecules which modulate FTO function are potentially novel remedies to the treatment of osteoporosis by adjusting the m6A levels. This article reviews the roles of m6A demethylase FTO in regulating bone metabolism and osteoporosis.

摘要

骨质疏松症是一种常见的骨骼疾病,其特征是由于骨稳态失调导致骨量下降。尽管不同的研究已经确定骨质疏松症与成骨基因的表观遗传改变之间存在关联,但骨质疏松症的发病机制仍不清楚。N6-甲基腺苷(m6A)修饰是一种甲基化的腺苷核苷酸,它调节RNA的转运、输出、翻译和降解。FTO是第一个被鉴定出的m6A去甲基化酶,它能消除RNA上的m6A修饰。FTO的变异会干扰RNA中的m6A甲基化,从而调节细胞增殖、分化和凋亡。此外,FTO作为一个与肥胖相关的基因,还通过调节脂肪生成来影响成骨作用。对FTO的药理学抑制显著改变了骨量、骨密度和脂肪组织的分布。调节FTO功能的小分子有可能通过调节m6A水平成为治疗骨质疏松症的新型药物。本文综述了m6A去甲基化酶FTO在调节骨代谢和骨质疏松症中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b549/10667916/ff8093d13c6b/fcell-11-1275475-g001.jpg

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