Deng Min, Jing Da-Dao, Meng Xiang-Jun
Department of Gastroenterology, Shanghai First People's Hospital, Shanghai Jiao Tong University, Shanghai, China.
Asian Pac J Cancer Prev. 2013;14(1):127-31. doi: 10.7314/apjcp.2013.14.1.127.
Trastuzumab is the first molecular targeting drug to increase the overall survival rate in advanced gastric cancer. However, it has also been found that a high intrinsic or primary trastuzumab resistance exists in some proportion of gastric cancer patients. In order to explore the mechanism of resistance to trastuzumab, firstly we investigated the expression of MUC1 (membrane-type mucin 1) in gastric cancer cells and its relationship with drug-resistance. Then using gene-silencing, we transfected a siRNA of MUC1 into drug-resistant cells. The results showed the MKN45 gastric cell line to be resistant to trastuzumab, mRNA and protein expression of MUC1 being significantly upregulated. After transfection of MUC1 siRNA, protein expression of MUC1 in MKN45cells was significantly reduced. Compared with the junk transfection and blank control groups, the sensitivity to trastuzumab under MUC1 siRNA conditions was significantly increased. These results imply that HER2-positive gastric cancer cell MKN45 is resistant to trastuzumab and this resistance can be cancelled by silencing expression of the MUC1 gene.
曲妥珠单抗是首个提高晚期胃癌总体生存率的分子靶向药物。然而,也发现部分胃癌患者存在较高比例的内在性或原发性曲妥珠单抗耐药。为探究曲妥珠单抗耐药机制,我们首先研究了MUC1(膜型黏蛋白1)在胃癌细胞中的表达及其与耐药性的关系。然后通过基因沉默,将MUC1的小干扰RNA转染至耐药细胞。结果显示MKN45胃癌细胞系对曲妥珠单抗耐药,MUC1的mRNA和蛋白表达显著上调。转染MUC1小干扰RNA后,MKN45细胞中MUC1的蛋白表达显著降低。与空载体转染组和空白对照组相比,MUC1小干扰RNA条件下对曲妥珠单抗的敏感性显著增加。这些结果表明HER2阳性胃癌细胞MKN45对曲妥珠单抗耐药,且这种耐药可通过沉默MUC1基因表达来消除。