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TUG1 mediates methotrexate resistance in colorectal cancer via miR-186/CPEB2 axis.TUG1通过miR-186/CPEB2轴介导结直肠癌对甲氨蝶呤的耐药性。
Biochem Biophys Res Commun. 2017 Sep 16;491(2):552-557. doi: 10.1016/j.bbrc.2017.03.042. Epub 2017 Mar 14.
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Direct binding of microRNA-21 pre-element with Regorafenib: An alternative mechanism for anti-colorectal cancer chemotherapy?微小RNA-21前体元件与瑞戈非尼的直接结合:抗结直肠癌化疗的一种替代机制?
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microRNA-577 suppresses tumor growth and enhances chemosensitivity in colorectal cancer.微小RNA-577抑制结直肠癌的肿瘤生长并增强其化疗敏感性。
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First-line therapy for mCRC - the influence of primary tumour location on the therapeutic algorithm.转移性结直肠癌的一线治疗——原发肿瘤部位对治疗方案的影响
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MALAT1 Is Associated with Poor Response to Oxaliplatin-Based Chemotherapy in Colorectal Cancer Patients and Promotes Chemoresistance through EZH2.MALAT1 与结直肠癌患者对奥沙利铂为基础的化疗反应不良相关,并通过 EZH2 促进化疗耐药性。
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Prognostic and predictive significance of long interspersed nucleotide element-1 methylation in advanced-stage colorectal cancer.长散在核元件-1甲基化在晚期结直肠癌中的预后及预测意义
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From tumour heterogeneity to advances in precision treatment of colorectal cancer.从肿瘤异质性到结直肠癌精准治疗的进展。
Nat Rev Clin Oncol. 2017 Apr;14(4):235-246. doi: 10.1038/nrclinonc.2016.171. Epub 2016 Dec 6.
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Prognostic and Predictive Relevance of Primary Tumor Location in Patients With RAS Wild-Type Metastatic Colorectal Cancer: Retrospective Analyses of the CRYSTAL and FIRE-3 Trials.RAS野生型转移性结直肠癌患者中原发肿瘤部位的预后和预测相关性:CRYSTAL和FIRE-3试验的回顾性分析
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The Clinical Significance of MiR-429 as a Predictive Biomarker in Colorectal Cancer Patients Receiving 5-Fluorouracil Treatment.MiR-429作为接受5-氟尿嘧啶治疗的结直肠癌患者预测生物标志物的临床意义
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Circulating Non-coding RNA as Biomarkers in Colorectal Cancer.循环非编码RNA作为结直肠癌的生物标志物
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非编码RNA作为转移性结直肠癌当前治疗的预测生物标志物

Non-Coding RNAs as Predictive Biomarkers to Current Treatment in Metastatic Colorectal Cancer.

作者信息

Garajová Ingrid, Ferracin Manuela, Porcellini Elisa, Palloni Andrea, Abbati Francesca, Biasco Guido, Brandi Giovanni

机构信息

Department of Experimental, Diagnostic and Specialty Medicine (DIMES), Sant'Orsola-Malpighi Hospital, University of Bologna, 40138 Bologna, Italy.

Interdepartmental Centre of Cancer Research "Giorgio Prodi", University of Bologna, 40138 Bologna, Italy.

出版信息

Int J Mol Sci. 2017 Jul 17;18(7):1547. doi: 10.3390/ijms18071547.

DOI:10.3390/ijms18071547
PMID:28714940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5536035/
Abstract

The onset and selection of resistant clones during cancer treatment with chemotherapy or targeted therapy is a major issue in the clinical management of metastatic colorectal cancer patients. It is possible that a more personalized treatment selection, using reliable response-to-therapy predictive biomarkers, could lead to an improvement in the success rate of the proposed therapies. Although the process of biomarker selection and validation could be a long one, requiring solid statistics, large cohorts and multicentric validations, non-coding RNAs (ncRNAs) and in particular microRNAs, proved to be extremely promising in this field. Here we summarize some of the main studies correlating specific ncRNAs with sensitivity/resistance to chemotherapy, anti-VEGF therapy, anti-EGFR therapy and immunotherapy in colorectal cancer (CRC).

摘要

在转移性结直肠癌患者的临床管理中,化疗或靶向治疗期间耐药克隆的出现和选择是一个主要问题。使用可靠的治疗反应预测生物标志物进行更个性化的治疗选择,有可能提高所提议治疗的成功率。尽管生物标志物的选择和验证过程可能很长,需要坚实的统计学、大型队列和多中心验证,但非编码RNA(ncRNAs),尤其是微小RNA,在该领域已被证明极具前景。在此,我们总结了一些将特定ncRNAs与结直肠癌(CRC)对化疗、抗血管内皮生长因子(VEGF)治疗、抗表皮生长因子受体(EGFR)治疗和免疫治疗的敏感性/耐药性相关联的主要研究。