Department of Clinical Laboratory, Qilu Hospital, Shandong University, Jinan, Shandong Province, China.
Department of Clinical Laboratory, Women & Children's Hospital of Linyi, Linyi, Shandong Province, China.
Mol Cancer Ther. 2017 Apr;16(4):739-751. doi: 10.1158/1535-7163.MCT-16-0591. Epub 2017 Jan 9.
A major reason for oxaliplatin chemoresistance in colorectal cancer is the acquisition of epithelial-mesenchymal transition (EMT) in cancer cells. The long noncoding RNA (lncRNA), MALAT1, is a highly conserved nuclear ncRNA and a key regulator of metastasis development in several cancers. However, its role in oxaliplatin-induced metastasis and chemoresistance is not well known. In this study, we aim to investigate the prognostic and therapeutic role of lncRNA MALAT1 in colorectal cancer patients receiving oxaliplatin-based therapy and further explore the potential transcriptional regulation through interaction with EZH2 based on the established HT29 oxaliplatin-resistant cells. Our results showed that high MALAT1 expression was associated with reduced patient survival and poor response to oxaliplatin-based chemotherapy in advanced colorectal cancer patients. Oxaliplatin-resistant colorectal cancer cells exhibited high MALAT1 expression and EMT. LncRNA MALAT1 knockdown enhances E-cadherin expression and inhibits oxaliplatin-induced EMT in colorectal cancer cells. EZH2 is highly expressed and associated with the 3' end region of lncRNA MALAT1 in colorectal cancer, and this association suppressed the expression of E-cadherin. Furthermore, targeted inhibition of MALAT1 or EZH2 reversed EMT and chemoresistance induced by oxaliplatin. Finally, the interaction between lncRNA MALAT1 and miR-218 was observed, which further indicated its prognostic value in patients who received standard FOLFOX (oxaliplatin combine with 5-fluorouracil and leucovorin) treatment. In conclusion, this study illuminates the prognostic role of lncRNA MALAT1 in colorectal cancer patients receiving oxaliplatin-based treatment and further demonstrates how lncRNA MALAT1 confers a chemoresistant function in colorectal cancer. Thus, lncRNA MALAT1 may serve as a promising prognostic and therapeutic target for colorectal cancer patients. .
在结直肠癌中,奥沙利铂化疗耐药的一个主要原因是癌细胞获得上皮-间充质转化(EMT)。长链非编码 RNA(lncRNA)MALAT1 是一种高度保守的核非编码 RNA,是几种癌症中转移发展的关键调节剂。然而,其在奥沙利铂诱导的转移和化疗耐药中的作用尚不清楚。在这项研究中,我们旨在研究 lncRNA MALAT1 在接受奥沙利铂为基础的治疗的结直肠癌患者中的预后和治疗作用,并进一步通过与 EZH2 的相互作用来探索潜在的转录调节,基于已建立的 HT29 奥沙利铂耐药细胞。我们的结果表明,MALAT1 高表达与晚期结直肠癌患者的生存时间缩短和对奥沙利铂为基础的化疗反应不良有关。奥沙利铂耐药结直肠癌细胞表现出高 MALAT1 表达和 EMT。lncRNA MALAT1 敲低可增强结直肠癌细胞中 E-钙粘蛋白的表达并抑制奥沙利铂诱导的 EMT。EZH2 在结直肠癌中高度表达并与 lncRNA MALAT1 的 3'端区域相关,这种关联抑制了 E-钙粘蛋白的表达。此外,靶向抑制 MALAT1 或 EZH2 逆转了奥沙利铂诱导的 EMT 和耐药性。最后,观察到 lncRNA MALAT1 与 miR-218 之间的相互作用,这进一步表明其在接受标准 FOLFOX(奥沙利铂联合 5-氟尿嘧啶和亚叶酸钙)治疗的患者中的预后价值。总之,本研究阐明了 lncRNA MALAT1 在接受奥沙利铂为基础治疗的结直肠癌患者中的预后作用,并进一步证明了 lncRNA MALAT1 如何在结直肠癌中赋予化疗耐药功能。因此,lncRNA MALAT1 可能成为结直肠癌患者有前途的预后和治疗靶点。