mirna在结直肠癌病理生物学中的临床作用综述

Q3 Medicine
Nahal Eshghifar, Elham Badrlou, Farkhondeh Pouresmaeili
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引用次数: 2

摘要

mirna (microRNAs)被定义为基因表达的微导演和调控者。由于改变的miRNA表达在多种癌症如结肠直肠癌(crc)的病理生物学中具有重要意义,因此这些分子也被描述为治疗靶点。mirna的操作可能导致化疗和放射耐药crc的进一步治疗。由于microRNAs独特的表达模式与癌症类型和恶性肿瘤相关,其在结直肠癌的预后和诊断中的应用显示出突出的前景。目前,许多研究者正在分析miRNA多态性与癌症风险的相关性。随着结直肠癌(CRC) miRNAs表达数据的持续不兼容性,向“实验室前”分析的内容迈进以加快高效、准确的医学和转化研究是至关重要的。通过对最高表达的miRNAs调控靶基因的通路研究,发现了大量与CRC通路相关的基因,包括PI3K、TGFβ和APC。在这篇综述中,我们旨在收集有关mirna及其在结直肠癌中的潜在作用的富有成效的信息,并对与该疾病相关的最常研究的mirna进行meta分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The roles of miRNAs' clinical efficiencies in the colorectal cancer pathobiology: A review article.

MiRNAs (microRNAs) are defined as micro directors and regulators of gene expression. Since altered miRNA expression is signified in the pathobiology of diverse cancers such as colorectal cancers (CRCs), these molecules are described as therapeutic targets, either. Manipulation of miRNAs could lead to further therapy for chemo and radio-resistant CRCs. The usage of microRNAs has indicated prominent promise in the prognosis and diagnosis of CRC, because of their unique expression pattern associated with cancer types and malignancies. Nowadays, many researchers are analyzing the correlation between miRNA polymorphisms and cancer risk. With continuous incompatibility in colorectal cancer (CRC) miRNAs expression data, it is critical to move toward the content of a "pre-laboratory" analysis to speed up efficient accuracy medicine and translational study. Pathway study for the highest expressed miRNAs- regulated target genes resulted in the identification of a considerable number of genes associated with CRC pathway including PI3K, TGFβ, and APC. In this review, we aimed to collect fruitful information about miRNAs and their potential roles in CRC, and provide a meta-analysis of the most frequently studied miRNAs in association with the disease.

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来源期刊
Human Antibodies
Human Antibodies Medicine-Immunology and Allergy
CiteScore
3.50
自引率
0.00%
发文量
27
期刊介绍: Human Antibodies is an international journal designed to bring together all aspects of human hybridomas and antibody technology under a single, cohesive theme. This includes fundamental research, applied science and clinical applications. Emphasis in the published articles is on antisera, monoclonal antibodies, fusion partners, EBV transformation, transfections, in vitro immunization, defined antigens, tissue reactivity, scale-up production, chimeric antibodies, autoimmunity, natural antibodies/immune response, anti-idiotypes, and hybridomas secreting interesting growth factors. Immunoregulatory molecules, including T cell hybridomas, will also be featured.
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