Department of General Surgery, The First Affiliated Hospital of Hebei North University, Zhangjiakou, China.
Department of Ultrasound, The First Affiliated Hospital of Hebei North University, Zhangjiakou, China.
Kaohsiung J Med Sci. 2019 Apr;35(4):209-213. doi: 10.1002/kjm2.12037. Epub 2019 Mar 19.
This study aims to explore the effect of an inhibitor of DNA binding-1 (Id-1) on the proliferation and migration of human colon carcinoma cell line SW480 and HT-29. SW480 and HT-29 cells transfected with Id-1-interference sequence were assigned to the experimental groups (inhibition groups 1 and 2), and SW480 and HT-29 cells with blank interference sequence (blank groups) and blank load transfection (blank load groups) were assigned as the control groups. The expression of Id-1 in six groups was detected by reverse transcription-polymerase chain reaction (RT-PCR) and Western blot. Cell proliferation in vitro was assessed by MTT assay. RT-PCR and Western blot results demonstrated that the mRNA and protein expressions of Id-1 in the inhibition group 1 were lower than those in the blank group 1 and blank load group 1. RT-PCR and Western blot results revealed that the mRNA and protein expressions of Id-1 were lower in the inhibition group 2 than in the blank group 2 and blank load group 2. The results of the growth curve revealed that proliferation ability was significantly weaker from the third day in the inhibition groups 1 and 2 than in the blank group and blank load group. Transwell chamber experiment and Matrigel invasion assay revealed that the number of Transwell cells significantly decreased in the inhibition groups 1 and 2 than in the blank groups and blank load groups (P < 0.01). Id-1 significantly promotes the proliferation and migration of human colon carcinoma cell lines SW480 and HT-29.
本研究旨在探讨 DNA 结合抑制因子-1(Id-1)对人结肠癌细胞系 SW480 和 HT-29 增殖和迁移的影响。转染 Id-1 干扰序列的 SW480 和 HT-29 细胞被分配到实验组(抑制组 1 和 2),而带有空白干扰序列的 SW480 和 HT-29 细胞(空白组)和空白负载转染(空白负载组)被分配为对照组。通过逆转录聚合酶链反应(RT-PCR)和 Western blot 检测六组中 Id-1 的表达。通过 MTT assay 评估体外细胞增殖。RT-PCR 和 Western blot 结果表明,抑制组 1 中的 Id-1mRNA 和蛋白表达低于空白组 1 和空白负载组 1。RT-PCR 和 Western blot 结果表明,抑制组 2 中的 Id-1mRNA 和蛋白表达低于空白组 2 和空白负载组 2。生长曲线结果表明,从第 3 天开始,抑制组 1 和 2 的增殖能力明显弱于空白组和空白负载组。Transwell 室实验和 Matrigel 侵袭实验表明,抑制组 1 和 2 的 Transwell 细胞数量明显少于空白组和空白负载组(P<0.01)。Id-1 显著促进人结肠癌细胞系 SW480 和 HT-29 的增殖和迁移。