Tian Qing-Shui, Li De-Chun
Department of General Surgery, First Affiliated Hospital of Soochow University, Suzhou, Jiangsu Province, China.
Saudi Med J. 2010 Jul;31(7):752-8.
To investigate the biological functions of reversion-inducing cysteine-rich protein with Kazal motifs (RECK) over-expression in pancreatic cancer cell line Panc-1.
This study was carried out in the Department of General Surgery, First Affiliated Hospital of Soochow University, Suzhou, Jiangsu, China from January to September 2009. The design of the study was to construct a recombinant lentivirus carrying the RECK gene (LV-RECK) to be used to infect Panc-1 cells, and investigate the biological functions of RECK in pancreatic cancer in vitro. The RECK expression was measured by real-time polymerase chain reaction (PCR) and Western blotting. Cell proliferation and apoptosis were examined by 3-(4,5-dimethylthiazole-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and flow cytometry. The ability of invasion was detected using Transwell chambers. The expression and activity of matrix metalloproteinase (MMP)-2 and matrix metalloproteinase-9 (MMP-9) was measured by real-time PCR, Western blotting, and gelatin zymography.
We successfully constructed LV-RECK and proved it can over-express the RECK gene in Panc-1 cells. The RECK over-expression potently suppressed the invasion ability of Panc-1 cells in vitro without affecting cell proliferation and apoptosis. The RECK over-expression potently inhibited the secretion and activity of MMP-2, and the secretion of MMP-9 without affecting the messenger ribonucleic acid, and protein expression of MMP-2 and MMP-9.
The RECK gene exerts repressive effects on the invasion ability of the pancreatic cancer cell line Panc-1, and it may be a novel therapeutic target for pancreatic cancer.
研究富含Kazal基序的逆转录诱导型富含半胱氨酸蛋白(RECK)在胰腺癌细胞系Panc-1中过表达的生物学功能。
本研究于2009年1月至9月在江苏省苏州市苏州大学附属第一医院普通外科进行。研究设计为构建携带RECK基因的重组慢病毒(LV-RECK)用于感染Panc-1细胞,并在体外研究RECK在胰腺癌中的生物学功能。通过实时聚合酶链反应(PCR)和蛋白质印迹法检测RECK表达。采用3-(4,5-二甲基噻唑-2)-2,5-二苯基四氮唑溴盐(MTT)法和流式细胞术检测细胞增殖和凋亡。使用Transwell小室检测侵袭能力。通过实时PCR、蛋白质印迹法和明胶酶谱法检测基质金属蛋白酶(MMP)-2和基质金属蛋白酶-9(MMP-9)的表达和活性。
我们成功构建了LV-RECK,并证明其可在Panc-1细胞中过表达RECK基因。RECK过表达在体外显著抑制Panc-1细胞的侵袭能力,而不影响细胞增殖和凋亡。RECK过表达显著抑制MMP-2的分泌和活性以及MMP-9的分泌,但不影响MMP-2和MMP-9的信使核糖核酸及蛋白表达。
RECK基因对胰腺癌细胞系Panc-1的侵袭能力具有抑制作用,可能是胰腺癌的一个新的治疗靶点。