更昔洛韦
遗传增强
肺癌
自杀基因
癌症研究
单纯疱疹病毒
生物
胸苷激酶
腺癌
癌症
基因传递
肺腺癌
免疫学
医学
病理
人巨细胞病毒
病毒
基因
生物化学
遗传学
作者
Ann‐Marie Määttä,Anni Tenhunen,Tiina Pasanen,Outi Meriläinen,Riikka Pellinen,Kimmo Mäkinen,Esko Alhava,Jarmo Wahlfors
出处
期刊:International Journal of Oncology
[Spandidos Publications]
日期:2004-04-01
卷期号:24 (4): 943-9
被引量:34
摘要
Lung cancer is a group of diseases that are difficult to cure and new treatment modalities, like gene therapy are actively tested to find alternatives for currently used strategies. Herpes simplex virus thymidine kinase/ganciclovir (HSV-TK/GCV) method is one of the most frequently utilized forms of gene therapy and it has been tested on lung cancer, but no systematic study with comparison of different lung cancer types has been published. In this study, we examined in vitro and in vivo how good targets non-small cell lung cancer (NSCLC) cell lines representing adenocarcinoma, squamous cell lung cancer and large cell lung cancer are for adenovirus-mediated HSV-TK/GCV gene therapy. By using an adenovirus vector carrying a fusion gene of HSV-TK and green fluorescent protein (GFP), we found that: a) adenoviruses were efficient gene transfer vehicles for all types of NSCLCs; b) all adenocarcinoma and large cell lung cancer cells were good targets for HSV-TK/GCV therapy, whereas one of the squamous cell carcinoma cell lines was not responsive to the treatment; c) bystander effect played a major role in the success of this gene therapy form; d) subcutaneous tumors representing all three NSCLC types were efficiently treated with adenovirus-mediated HSV-TK/GCV gene therapy. In summary, this form of gene therapy appeared to be efficient treatment for human NSCLC and these results warrant further studies with primary lung cancer cells and orthotopic lung tumor models.
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