甲基转移酶样 3 是诊断和治疗肾脏疾病的前瞻性靶点。

IF 3.8 3区 医学 Q2 GENETICS & HEREDITY Human Genomics Pub Date : 2024-11-14 DOI:10.1186/s40246-024-00692-8
Bin Song, Xiaolong Wu, Yan Zeng
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引用次数: 0

摘要

肾脏疾病病理机制复杂,治疗难度大,导致全球发病率和死亡率居高不下。深入了解其中的基本过程有助于确定新的治疗靶点并提高治疗效果。目前的综合数据分析表明,甲基转移酶样 3(METTL3)及其在 RNA N6-甲基腺苷甲基化中的作用参与了各种肾脏病理,包括急性肾损伤、肾脏纤维化和慢性肾病。然而,阐明 METTL3 的功能机制并评估其在提高治疗效果方面的重要性的详尽综述并不多见。本综述旨在系统研究 METTL3 在肾脏疾病中的作用、机制和潜在的临床应用。研究结果表明,METTL3 与肾脏疾病的病因和恶化有关,它通过调节特定的遗传途径影响肾脏疾病的发病、进展、恶性程度以及对化疗药物的反应性。总之,这篇综述强调了 METTL3 与肾脏疾病之间的有害关联,突出了靶向 METTL3 的治疗前景。此外,它还为研究人员提供了有关肾脏疾病诊断、预后和治疗策略的重要见解。
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Methyltransferase-like 3 represents a prospective target for the diagnosis and treatment of kidney diseases.

Kidney disease is marked by complex pathological mechanisms and significant therapeutic hurdles, resulting in high morbidity and mortality rates globally. A deeper understanding of the fundamental processes involved can aid in identifying novel therapeutic targets and improving treatment efficacy. Current comprehensive data analyses indicate the involvement of methyltransferase-like 3 (METTL3) and its role in RNA N6-methyladenosine methylation in various renal pathologies, including acute kidney injury, renal fibrosis, and chronic kidney disease. However, there is a paucity of thorough reviews that clarify the functional mechanisms of METTL3 and evaluate its importance in enhancing therapeutic outcomes. This review seeks to systematically examine the roles, mechanisms, and potential clinical applications of METTL3 in renal diseases. The findings presented suggest that METTL3 is implicated in the etiology and exacerbation of kidney disorders, affecting their onset, progression, malignancy, and responsiveness to chemotherapeutic agents through the regulation of specific genetic pathways. In conclusion, this review underscores a detrimental correlation between METTL3 and kidney diseases, highlighting the therapeutic promise of targeting METTL3. Additionally, it offers critical insights for researchers concerning the diagnosis, prognosis, and treatment strategies for renal conditions.

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来源期刊
Human Genomics
Human Genomics GENETICS & HEREDITY-
CiteScore
6.00
自引率
2.20%
发文量
55
审稿时长
11 weeks
期刊介绍: Human Genomics is a peer-reviewed, open access, online journal that focuses on the application of genomic analysis in all aspects of human health and disease, as well as genomic analysis of drug efficacy and safety, and comparative genomics. Topics covered by the journal include, but are not limited to: pharmacogenomics, genome-wide association studies, genome-wide sequencing, exome sequencing, next-generation deep-sequencing, functional genomics, epigenomics, translational genomics, expression profiling, proteomics, bioinformatics, animal models, statistical genetics, genetic epidemiology, human population genetics and comparative genomics.
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