Wu Jin-bao, Nan Qing-zhen, Ma Gao-feng, Gong Wei, Chen Lin, Lin Ying-zhuo, Wang Ji-de, Zhang Hong-quan, Song Yu-gang
Institute of Digestive Diseases, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2007 Jul;27(7):951-4.
To investigate the effect of short hairpin RNA (shRNA) targeting survivin on adhesion and invasion of human colon carcinoma cell line SW480 in vitro.
According to the sequence of the coding region of survivin gene, two strings of 19 nucleotides of inverted sequence flanking the loop sequence of two complementary 9-base oligonucleotides were designed and synthesized to prepare the hairpin construct as the DNA templates for the target shRNA. The shRNA templates were cloned into shRNA expression vector pRNAT-U6.1/Neo, and the resulted vector pRNAT-U6.1/Neo-survivin was transfected into SW480 cells using Lipofectamine 2000. Western blotting was performed to evaluate survivin gene silencing induced by shRNA transfection at the protein level, and the biological behaviors of the SW480 cells were investigated by cell-matrix adhesion, invasion and gelatin-zymography assays.
Western blotting revealed significantly lowered survivin protein expression in transfected SW480 cells, and survivin gene silencing induced by shRNA significantly suppressed the metastatic potential of SW480 cells in association with suppressed MMPs activity.
Survivin may play an important role in modulating human colorectal carcinoma cell invasion and metastasis, and survivin gene silencing can inhibit human colorectal cancer cell invasion and the production of MMP-2 and MMP-9. Survivin may affect invasion and metastasis of human colorectal carcinoma cells via regulating the production of MMPs.
探讨靶向生存素的短发夹RNA(shRNA)对人结肠癌细胞系SW480体外黏附及侵袭能力的影响。
根据生存素基因编码区序列,设计并合成两段19个核苷酸的反向序列,分别位于两个互补的9碱基寡核苷酸环序列两侧,制备发夹结构作为靶shRNA的DNA模板。将shRNA模板克隆至shRNA表达载体pRNAT-U6.1/Neo中,采用Lipofectamine 2000将构建成功的载体pRNAT-U6.1/Neo-survivin转染至SW480细胞。通过蛋白质印迹法在蛋白质水平评估shRNA转染诱导的生存素基因沉默情况,并采用细胞-基质黏附、侵袭及明胶酶谱分析等方法研究SW480细胞的生物学行为。
蛋白质印迹法显示,转染后的SW480细胞中生存素蛋白表达显著降低,shRNA诱导的生存素基因沉默与基质金属蛋白酶(MMPs)活性受抑制相关,显著抑制了SW480细胞的转移潜能。
生存素可能在调节人结肠癌细胞侵袭和转移中发挥重要作用,生存素基因沉默可抑制人结肠癌细胞侵袭及MMP-2和MMP-9的产生。生存素可能通过调节MMPs的产生影响人结肠癌细胞的侵袭和转移。