Liu Quan, Zhao Xin-Yu, Bai Rui-Zhen, Liang Shu-Fang, Nie Chun-Lai, Yuan Zhu, Wang Chun-Ting, Wu Yang, Chen Li-Juan, Wei Yu-Quan
State Key Laboratory of Biotherapy, West China Hospital, West China Medical School, Sichuan University, Chengdu 610041, PR China.
Oncol Rep. 2009 Nov;22(5):1069-75.
Down-regulated in renal cell carcinoma gene (DRR1) is one of the candidate tumor suppressor genes (TSGs) on human 3p21.1. This study was performed to validate the expression status of DRR1 gene in cancer cells and the expression pattern of the protein in clinical specimens of human lung cancer and to examine its potential as a molecular target for treatment of lung cancer in vivo. DRR1 expression was analyzed in 7 human lung cancer cell lines. DRR1 protein expression was also examined in clinical non-small cell lung cancer (NSCLC) specimens. Furthermore, effects of DRR1 re-expression on A549 cells in vitro and A549 xenograft tumors in nude mice were evaluated. Loss of DRR1 mRNA expression was detected in 6 of the 7 human cancer cell lines, the exception was the renal cancer cell line OS-RC-2. DRR1 protein expression was absent in 15 of 20 (75%) human NSCLC specimens by immunostaining. Transfection of DRR1 gene into DRR1-negative-expressing A549 cells resulted in significant cell growth suppression and apoptosis. Plasmids containing DRR1 cDNA complexed with DOTAP:Chol liposomes were administered intravenously via tail vein to nude mice bearing A549 xenograft tumors resulting in tumor growth inhibition and elevation of apoptosis compared with the controls. DRR1 is a potent growth suppressor of NSCLC, acting through apoptosis pathway in vivo and it may be a potential therapeutic gene for human lung cancer.
肾细胞癌下调基因(DRR1)是位于人类3p21.1上的候选肿瘤抑制基因(TSG)之一。本研究旨在验证DRR1基因在癌细胞中的表达状态以及该蛋白在人肺癌临床标本中的表达模式,并检测其作为肺癌体内治疗分子靶点的潜力。分析了7种人肺癌细胞系中的DRR1表达情况。还检测了临床非小细胞肺癌(NSCLC)标本中的DRR1蛋白表达。此外,评估了DRR1重新表达对体外A549细胞和裸鼠体内A549异种移植瘤的影响。在7种人癌细胞系中的6种中检测到DRR1 mRNA表达缺失,例外的是肾癌细胞系OS-RC-2。通过免疫染色,在20例人NSCLC标本中的15例(75%)中未检测到DRR1蛋白表达。将DRR1基因转染到DRR1表达阴性的A549细胞中导致显著的细胞生长抑制和凋亡。将含有DRR1 cDNA并与DOTAP:Chol脂质体复合的质粒经尾静脉静脉注射给携带A549异种移植瘤的裸鼠,与对照组相比,导致肿瘤生长抑制和凋亡增加。DRR1是NSCLC的一种有效的生长抑制因子,在体内通过凋亡途径发挥作用,它可能是人类肺癌的一个潜在治疗基因。