In vitro and in vivo growth inhibition of drug-resistant ovarian carcinoma cells using a combination of cisplatin and a TRAIL-encoding retrovirus.
In vitro and in vivo growth inhibition of drug-resistant ovarian carcinoma cells using a combination of cisplatin and a TRAIL-encoding retrovirus.
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使用顺铂和编码 TRAIL 的逆转录病毒的组合在体外和体内抑制耐药卵巢癌细胞的生长。
DOI:
10.3892/ol.2012.926
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发表时间:
2012
期刊:
影响因子:
2.9
通讯作者:
X. Wen
中科院分区:
文献类型:
--
作者:
Fang Li;Yi Guo;Ling;Yankang Duan;Fang Fang;S. Niu;Qiujie Ba;Huaishi Zhu;Fanfei Kong;Chao Lin;X. Wen
Retroviruses encoding the TNF-related apoptosis-inducing ligand (TRAIL) gene were generated by transient transfection of the retrovirus packing cell line BOSC 23 using TRAIL-encoding plasmid. The retrovirus was able to transduce drug-resistant A2780/DDP ovarian carcinoma cells in vitro and induce TRAIL expression in the cells, as detected by western blot assay. Furthermore, the TRAIL protein led to the growth inhibition of the cells via a caspase-activated apoptotic mechanism. It was confirmed that exposure of such cells to cisplatin in combination with the TRAIL-encoding retrovirus resulted in higher anticancer activity in vitro and in the xenograft A2780/DDP tumor in a nude mouse model. This study suggests that chemotherapy in combination with TRAIL gene therapy may be an efficient approach to treat drug-resistant ovarian cancer.
DOI:
10.1073/pnas.90.18.8392
发表时间:
1993-09-15
影响因子:
11.1
作者:
PEAR, WS;NOLAN, GP;BALTIMORE, D
通讯作者:
BALTIMORE, D