Department of Oncology and Radiotherapeutics, Faculty of Medicine and University Hospital in Pilsen, Charles University, Pilsen, Czech Republic
Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Cancer Genomics Proteomics. 2020 Sep-Oct;17(5):605-613. doi: 10.21873/cgp.20217.
BACKGROUND/AIM: MicroRNAs (miRs) play an important role in the regulation of cancer-related processes and are promising candidates for cancer biomarkers. The aim of the study was to evaluate the association of response to anti-EGFR monoclonal antibodies (mAbs) with selected miR expression profiles, including miR-125b, let-7c, miR-99a, miR-17, miR-143 and miR-145 in metastatic colorectal cancer (mCRC) patients.
This retrospective study included 46 patients with mCRC harbouring wild-type RAS gene treated with cetuximab or panitumumab combined with chemotherapy in first- or second-line therapy. The miR expression was assessed using qRT-PCR.
Down-regulation of miR-125b and let-7c and up-regulation of miR-17 were found in the tumour tissue (p=0.0226, p=0.0040, p<0.0001). Objective response rate (ORR) was associated with up-regulation of miR-125b (p=0.0005). Disease control rate (DCR) was associated with up-regulation of miR-125b and let-7c (p=0.0383 and p=0.0255) and down-regulation of miR-17 (p=0.0464). MiR-125b showed correlation with progression-free and overall survival (p=0.055 and p=0.006).
The results show that up-regulation of miR-125b is associated with higher ORR and DCR and longer survival; let-7c up-regulation and miR-17 down-regulation are associated with higher DCR in mCRC patients treated with anti-EGFR mAbs.
背景/目的:微小 RNA(miRs)在调控癌症相关过程中发挥着重要作用,是癌症生物标志物的有前途的候选者。本研究旨在评估抗 EGFR 单克隆抗体(mAbs)治疗转移性结直肠癌(mCRC)患者的疗效与选定 miR 表达谱之间的关联,包括 miR-125b、let-7c、miR-99a、miR-17、miR-143 和 miR-145。
本回顾性研究纳入了 46 例携带野生型 RAS 基因的 mCRC 患者,他们接受了西妥昔单抗或帕尼单抗联合化疗作为一线或二线治疗。使用 qRT-PCR 评估 miR 表达。
在肿瘤组织中发现 miR-125b 和 let-7c 的下调和 miR-17 的上调(p=0.0226,p=0.0040,p<0.0001)。客观缓解率(ORR)与 miR-125b 的上调相关(p=0.0005)。疾病控制率(DCR)与 miR-125b 和 let-7c 的上调(p=0.0383 和 p=0.0255)以及 miR-17 的下调相关(p=0.0464)。miR-125b 与无进展生存期和总生存期相关(p=0.055 和 p=0.006)。
结果表明,miR-125b 的上调与更高的 ORR 和 DCR 以及更长的生存时间相关;let-7c 的上调和 miR-17 的下调与接受抗 EGFR mAbs 治疗的 mCRC 患者的更高 DCR 相关。