Zhang Hao, Liang Chen, Hou Xinxin, Wang Ling, Zhang Dongsheng
Department of Imaging and Nuclear Medicine, Medical School of Southeast University, Nanjing, Jiangsu, People's Republic of China.
Department of Pathology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, People's Republic of China.
Int J Nanomedicine. 2016 Mar 15;11:1039-50. doi: 10.2147/IJN.S98519. eCollection 2016.
Combination therapy for lung cancer has garnered widespread attention. Radiation therapy, gene therapy, and molecular targeted therapy for lung cancer have certain effects, but the disadvantages of these treatment methods are evident. Combining these methods can decrease their side effects and increase their curative effects. In this study, we constructed a pYr-ads-8-5HRE-cfosp-iNOS-IFNG plasmid (a gene circuit that can express IFNγ), which is a gene circuit, and used that plasmid together with C225 (cetuximab) to prepare gene-loaded immunomagnetic albumin nanospheres (IMANS). Moreover, we investigated the therapeutic effects of gene-loaded IMANS in combination with radiation therapy on human lung cancer in vitro and in vivo. The results showed that this gene circuit was successively constructed and confirmed that the expression of INFγ was increased due to the gene circuit. Gene-loaded IMANS combined with radiation therapy demonstrated improved results in vitro and in vivo. In conclusion, gene-loaded IMANS enhanced the efficacy of combination therapy, solved problems related to gene transfer, and specifically targeted lung cancer cells.
肺癌的联合治疗已引起广泛关注。肺癌的放射治疗、基因治疗和分子靶向治疗都有一定疗效,但这些治疗方法的缺点也很明显。将这些方法联合起来可以减少其副作用并提高疗效。在本研究中,我们构建了一种pYr-ads-8-5HRE-cfosp-iNOS-IFNG质粒(一种可表达IFNγ的基因回路),并将该质粒与C225(西妥昔单抗)一起用于制备载基因免疫磁白蛋白纳米球(IMANS)。此外,我们研究了载基因IMANS联合放射治疗对人肺癌的体内外治疗效果。结果表明,该基因回路成功构建,并证实由于该基因回路,INFγ的表达增加。载基因IMANS联合放射治疗在体内外均显示出更好的效果。总之,载基因IMANS增强了联合治疗的疗效,解决了与基因转移相关的问题,并特异性靶向肺癌细胞。