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探讨 microRNA-409-3p 在肿瘤进展中的分子机制:迈向靶向治疗(综述)。

Investigating the molecular mechanisms of microRNA‑409‑3p in tumor progression: Towards targeted therapeutics (Review).

机构信息

Department of Clinical Laboratory, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266000, P.R. China.

Department of Cardiology, Tianjin Medical University General Hospital, Tianjin 300052, P.R. China.

出版信息

Int J Oncol. 2024 Jul;65(1). doi: 10.3892/ijo.2024.5655. Epub 2024 May 17.

Abstract

MicroRNAs (miRNAs) are a group of non‑coding RNAs that exert master regulatory functions in post‑-transcriptional gene expression. Accumulating evidence shows that miRNAs can either promote or suppress tumorigenesis by regulating different target genes or pathways and may be involved in the occurrence of carcinoma. miR‑409‑3p is dysregulated in a variety of malignant cancers. It plays a fundamental role in numerous cellular biological processes, such as cell proliferation, apoptosis, migration, invasion, autophagy, angiogenesis and glycolysis. In addition, studies have shown that miR‑409‑3p is expected to become a non‑invasive biomarker. Identifying the molecular mechanisms underlying miR‑409‑3p‑mediated tumor progression will help investigate miR‑409‑3p‑based targeted therapy for human cancers. The present review comprehensively summarized the recently published literature on miR‑409‑3p, with a focus on the regulation and function of miR‑409‑3p in various types of cancer, and discussed the clinical implications of miR‑409‑3p, providing new insight for the diagnosis and treatment of cancers.

摘要

微小 RNA(miRNA)是一组非编码 RNA,在后转录基因表达中发挥主要的调控功能。越来越多的证据表明,miRNA 可以通过调节不同的靶基因或途径促进或抑制肿瘤发生,并且可能参与癌的发生。miR-409-3p 在多种恶性肿瘤中失调。它在许多细胞生物学过程中发挥着基本作用,如细胞增殖、凋亡、迁移、侵袭、自噬、血管生成和糖酵解。此外,研究表明,miR-409-3p 有望成为一种非侵入性的生物标志物。鉴定 miR-409-3p 介导的肿瘤进展的分子机制将有助于研究基于 miR-409-3p 的针对人类癌症的靶向治疗。本综述全面总结了最近发表的关于 miR-409-3p 的文献,重点介绍了 miR-409-3p 在各种类型癌症中的调节和功能,并讨论了 miR-409-3p 的临床意义,为癌症的诊断和治疗提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/426e/11155714/4aa2e4e8ee1e/ijo-65-01-05655-g00.jpg

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