Microproteins/micropeptides dysregulation contributes to cancer progression and development: A mechanistic review

IF 3.3 3区 生物学 Q3 CELL BIOLOGY
Paul Rodrigues, Harun Bangali, Eyhab Ali, M. K. Sharma, Bekhzod Abdullaev, Adnan Taan Alkhafaji, Maha Medha Deorari, Rahman S. Zabibah, Ali Haslany
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引用次数: 0

Abstract

Microproteins, known as micropeptides, are small protein molecules encoded by short open reading frames. These recently identified molecules have been proven to be an essential part of the human proteome that participates in multiple processes, such as DNA repair, mitochondrial respiration, and regulating different signaling pathways. A growing body of studies has evidenced that microproteins exhibit dysregulated expression levels in various malignancies and contribute to tumor progression. It has been reported that microproteins interact with many proteins, such as enzymes (e.g., adenosine triphosphate synthase) and signal transducers (e.g., c-Jun), and regulate malignant cell metabolism, proliferation, and metastasis. Moreover, microproteins have been found to play a significant role in multidrug resistance in vitro and in vivo by their activity in DNA repair pathways. Considering that, this review intended to summarize the roles of microproteins in different aspects of tumorigenesis with diagnostic and therapeutic perspectives.

微蛋白/微肽失调导致癌症进展和发展:机理综述。
微蛋白,又称微肽,是由短开放阅读框编码的小分子蛋白质。这些新近发现的分子已被证明是人类蛋白质组的重要组成部分,参与了 DNA 修复、线粒体呼吸和调节不同信号通路等多个过程。越来越多的研究证明,微蛋白在各种恶性肿瘤中的表达水平失调,并导致肿瘤进展。据报道,微蛋白与许多蛋白质相互作用,如酶(如三磷酸腺苷合成酶)和信号转导因子(如 c-Jun),并调控恶性细胞的新陈代谢、增殖和转移。此外,研究还发现,微蛋白通过在 DNA 修复途径中的活性,在体外和体内的多药耐药性中发挥着重要作用。有鉴于此,本综述旨在从诊断和治疗的角度总结微量蛋白在肿瘤发生的不同方面的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cell Biology International
Cell Biology International 生物-细胞生物学
CiteScore
7.60
自引率
0.00%
发文量
208
审稿时长
1 months
期刊介绍: Each month, the journal publishes easy-to-assimilate, up-to-the minute reports of experimental findings by researchers using a wide range of the latest techniques. Promoting the aims of cell biologists worldwide, papers reporting on structure and function - especially where they relate to the physiology of the whole cell - are strongly encouraged. Molecular biology is welcome, as long as articles report findings that are seen in the wider context of cell biology. In covering all areas of the cell, the journal is both appealing and accessible to a broad audience. Authors whose papers do not appeal to cell biologists in general because their topic is too specialized (e.g. infectious microbes, protozoology) are recommended to send them to more relevant journals. Papers reporting whole animal studies or work more suited to a medical journal, e.g. histopathological studies or clinical immunology, are unlikely to be accepted, unless they are fully focused on some important cellular aspect. These last remarks extend particularly to papers on cancer. Unless firmly based on some deeper cellular or molecular biological principle, papers that are highly specialized in this field, with limited appeal to cell biologists at large, should be directed towards journals devoted to cancer, there being very many from which to choose.
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