Li Jing, Mo Rubing, Zheng Linmei
Department of Emergency Surgery, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, 570311, Hainan Province, China.
Department of Pneumology, Hainan General Hospital, Hainan Affiliated Hospital of Hainan Medical University, Haikou, 570311, Hainan Province, China.
World J Surg Oncol. 2021 Apr 13;19(1):117. doi: 10.1186/s12957-021-02226-1.
Colorectal cancer is one of the most common malignancy in the world. The oncogenesis of colorectal cancer is still not fully elucidated. It was reported that microRNA-490-3p (miR-490-3p) was closely related to the regulation of cancers. However, if miR-490-3p could also affect colorectal cancer and the specific mechanism remains unclear.
qRT-PCR was conducted to examine the expression of miR-490-3p. DIANA, miRDB, and TargetScan databases were used to identify target genes. LOVO and SW480 cells were transfected by miR-490-3p mimics and inhibitors. Transwell assay was used to measure cell invasion and migration. Cisplatin and fluorouracil were administered to investigate chemotherapy resistance. Western blot was used to measure TNKS2 protein expression. Binding sites were verified using the double luciferase assay.
miR-490-3p expression was low in the colorectal cancer cells. The level of miR-490-3p was negatively correlated with cell migration and invasion of cancer cells. miR-490-3p could bind to TNKS2 mRNA 3'UTR directly. miR-490-3p can suppress cell viability and resistance to chemotherapy in colorectal cancer cells through targeting TNKS2.
miR-490-3p could affect colorectal cancer by targeting TNKS2. This study may provide a potential therapeutic target for colorectal cancer.
结直肠癌是世界上最常见的恶性肿瘤之一。结直肠癌的肿瘤发生机制仍未完全阐明。据报道,微小RNA-490-3p(miR-490-3p)与癌症的调控密切相关。然而,miR-490-3p是否也能影响结直肠癌及其具体机制尚不清楚。
采用qRT-PCR检测miR-490-3p的表达。利用DIANA、miRDB和TargetScan数据库鉴定靶基因。用miR-490-3p模拟物和抑制剂转染LOVO和SW480细胞。采用Transwell实验检测细胞侵袭和迁移能力。给予顺铂和氟尿嘧啶以研究化疗耐药性。采用蛋白质免疫印迹法检测TNKS2蛋白表达。使用双荧光素酶报告基因检测法验证结合位点。
miR-490-3p在结直肠癌细胞中表达较低。miR-490-3p水平与癌细胞的迁移和侵袭呈负相关。miR-490-3p可直接与TNKS2 mRNA的3'UTR结合。miR-490-3p可通过靶向TNKS2抑制结直肠癌细胞的活力和化疗耐药性。
miR-490-3p可通过靶向TNKS2影响结直肠癌。本研究可能为结直肠癌提供一个潜在的治疗靶点。