溶瘤病毒
端粒酶逆转录酶
端粒酶
溶癌病毒
癌症研究
端粒
癌变
生物
溶瘤腺病毒
病毒载体
癌细胞
癌症
基因
肿瘤细胞
重组DNA
遗传学
作者
Toshiyoshi Fujiwara,Shunsuke Kagawa,Hiroshi Tazawa
标识
DOI:10.2174/138920112800958887
摘要
Replication-selective tumor-specific viruses present a novel approach for treatment of neoplastic disease. These vectors are designed to induce virus-mediated lysis of tumor cells after selective viral propagation within the tumor. Telomerase activation is considered to be a critical step in carcinogenesis through the maintenance of telomeres, and its activity correlates closely with human telomerase reverse transcriptase (hTERT) expression. We constructed an attenuated adenovirus 5 vector, in which the hTERT promoter element drives expression of E1 genes, OBP-301 (Telomelysin). Since only tumor cells that express telomerase activity would activate this promoter, the hTERT proximal promoter allows for preferential expression of viral genes in tumor cells, leading to selective viral replication and oncolytic cell death. OBP-301 alone exhibited substantial antitumor effects both in animal models and in clinical trials; data regarding combination therapy with OBP-301 and chemotherapeutic agents are preliminary but encouraging. This article reviews synergistic interaction of virotherapy and chemotherapy, and illustrates the potential application for the treatment of human cancer.
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