微 RNA 作为乳腺癌药物敏感性生物标志物的潜在作用综述

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摘要

MiR-202是let-7家族的一部分,在细胞分裂和肿瘤发生中发挥作用,尤其是在女性乳腺癌(BC)中。我们对新的生物标志物进行了详细综述,以加强乳腺癌筛查并实现早期诊断,尤其是对年轻女性而言。早期检测和监测药物反应对乳腺癌的最佳治疗至关重要,因此需要新的生物标志物来诊断和预后。本综述将讨论在检测、分析和治疗乳腺癌(miRNA-BC)方面的最新研究成果。尽管乳腺癌患者通常以放疗开始治疗,但放疗效果可能会随着放射耐药性的出现而下降。本综述研究比较了多西他赛耐药乳腺癌(DRBC)和多西他赛敏感细胞系,探讨了非编码RNA,特别是环状RNA(circRNA)在DRBC发展中的作用,并确定了含紫杉类药物疗法的预测性生物标志物。微RNA测序和生物信息学可预测乳腺癌细胞类型之间在微RNA表达、基因和通路方面的差异。目前的证据表明,miR-202 的失调与信号通路有关,会影响其抗肿瘤或促肿瘤作用,从而显示出其作为诊断生物标志物的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Review of Potential Roles for Micro RNAs as Drugs Sensitivity Biomarkers in Breast Cancer
MiR-202, part of the let-7 family, plays a role in cell division and tumor development, especially in breast cancer (BC) among females. We have conducted a detailed review on new biomarkers to enhance BC screening and enable early diagnosis, particularly in younger women. Early detection and monitoring drug responses are crucial for optimal BC therapy, prompting the need for new biomarkers in diagnosis and prognosis. This review discusses recent findings on microRNAs in detecting, analyzing, and treating breast cancer (miRNA-BC). Although breast cancer patients often start treatment with radiotherapy, its effectiveness may decline with radiation resistance. This review study compares docetaxel-resistant breast cancer (DRBC) and docetaxel-sensitive cell lines, exploring the role of non-coding RNAs, especially circular RNAs (circRNAs), in DRBC development and identifying predictive biomarkers for taxane-containing therapies. MicroRNA sequencing and bioinformatics predict differences in microRNA expression, genes, and pathways between breast cancer cell types. Current evidence suggests that miR-202 dysregulation is linked to signaling pathways, influencing its anti- or pro-tumorigenic effects, showcasing its potential as a diagnostic biomarker.
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