Zhang Zhao-Yang, Xu Ke-Sen, Yang Guang-Yun, Wang Jin-Shen, Gao Ying, Liu Yan-Feng, Shuai Jing, Wang Jia-Yong, Li Shao-Yan, Shou Nan-Hai, Niu Jun
Department of General Surgery, Qilu Hospital of Shandong University, Jinan 250012, China.
Zhonghua Yi Xue Za Zhi. 2007 Oct 9;87(37):2645-8.
To investigate the effect of antisense integrin beta6 gene on the growth of colon cancer cells.
Expressing vector of antisense alphavbeta6 was constructed. Human colon cancer cells of the line HT29 were cultured and divided into 3 groups: Group A, remaining wild type; Group B, transfected with antisense integrin beta6 gene; and Group C, transfected with blank vector. RT-PCR was used to detect the integrin beta6 mRNA expression of in the HT29 cells. The integrinbeta6 protein expression on the surface of the cells was detected by immunohistochemistry and flow cytometry. The binding between the cells and fibronectin was examined. (3)H-labeled thymidine (T) was added into the culture fluid of the cells, and then the radiation amount was detected every 6 days so as to determine the capacity to proliferation of the cells in vitro. Thirty female nude mice were divided into 3 groups to be injected subcutaneously with suspension of HT29 cells of Groups A, B, and C as mentioned above. Six weeks later the size of tumors was measured and part of the tumor nodules were resected 5 weeks after the inoculation to undergo pathological examination.
Compared with Groups A and C, no corresponding band at 141 bp was found in Group B by RT-PCR. Flow cytometry showed that the expression level of beta6 protein had was (0.30 +/- 0.051, 30%), significantly lower than those of Groups A and C [(0.80 +/- 0.038, 80%) and (0.85 +/- 0.045, 85%), both P < 0.01]. The binding between the HT29 cells and fibronectin of Group B was significantly degraded after the further addition of anti-beta1 and anti-alphav in comparison of Groups A and C (both P < 0.01). The accumulation values of (3)H-labeled T of Group B 2, 4, and 6 days after addition were all significantly lower than those of Groups A and C (all P < 0.01). The tumors in 9 of the 10 mice injected with the HT29 cells of Group B disappeared and the tumor in the only one mice in Group B was only less than 1 mm(3), significantly smaller then those in Groups A and C (15 mm(3) on average, all P < 0.01).
Antisense beta6 gene significantly inhibits the mRNA and protein expression of the beta6 gene, and then inhibits the growth and proliferation of colon cancer cells, thus proving that integrin beta6 plays an important role in the regulation of colon cancer cells.
研究反义整合素β6基因对结肠癌细胞生长的影响。
构建反义αvβ6表达载体。培养人结肠癌细胞系HT29并分为3组:A组,保持野生型;B组,转染反义整合素β6基因;C组,转染空白载体。采用RT-PCR检测HT29细胞中整合素β6 mRNA表达。通过免疫组织化学和流式细胞术检测细胞表面整合素β6蛋白表达。检测细胞与纤连蛋白之间的结合情况。向细胞培养液中加入³H标记的胸腺嘧啶核苷(T),然后每6天检测放射量,以确定细胞的体外增殖能力。将30只雌性裸鼠分为3组,分别皮下注射上述A、B、C组的HT29细胞悬液。6周后测量肿瘤大小,接种后5周切除部分肿瘤结节进行病理检查。
RT-PCR结果显示,与A组和C组相比,B组未发现141 bp的相应条带。流式细胞术显示,β6蛋白表达水平为(0.30±0.051,30%),显著低于A组和C组[(0.80±0.038,80%)和(0.85±0.045,85%),均P<0.01]。与A组和C组相比,进一步加入抗β1和抗αv后,B组HT29细胞与纤连蛋白之间的结合明显减弱(均P<0.01)。加入³H标记的T后2、4和6天,B组的累积值均显著低于A组和C组(均P<0.01)。注射B组HT29细胞的10只小鼠中有9只肿瘤消失,B组仅1只小鼠的肿瘤小于1 mm³,明显小于A组和C组(平均15 mm³,均P<0.01)。
反义β6基因显著抑制β6基因的mRNA和蛋白表达,进而抑制结肠癌细胞的生长和增殖,从而证明整合素β6在结肠癌细胞的调控中起重要作用。