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Recombinant adenovirus-p53 (Gendicine) sensitizes a pancreatic carcinoma cell line to radiation

  
@article{CJCR3076,
	author = {Jinluan Li and Jianji Pan and Xianggao Zhu and Ying Su and Lingling Bao and Sufang Qiu and Changyan Zou and Yong Cai and Junxin Wu and Ivan W.K. Tham},
	title = {Recombinant adenovirus-p53 (Gendicine) sensitizes a pancreatic carcinoma cell line to radiation},
	journal = {Chinese Journal of Cancer Research},
	volume = {25},
	number = {6},
	year = {2013},
	keywords = {},
	abstract = {Objective: In this study, we examine the effects of recombinant adenovirus-p53 (rAd-p53) on the pancreatic carcinoma cell line SW1990. Specifically, we determine if expression of rAd-p53 sensitizes these cells to radiation. 
Methods: Following transfection of SW1990 cells with rAd-p53, we measured expression of P53, P21 and Bax by immunocytochemistry. Both transfected and control cell lines were irradiated with a range of doses, and the survival fractions (SF) were calculated. Dose survival curves were constructed and modeled for comparison. 
Results: Transfection of SW1990 cells with rAd-p53 resulted in increased expression of P53, P21 and Bax in a time-dependent manner. At 96 h after transfection, 89.92% of cells expressed P53, 56.8% expressed P21, and 76.50% expressed Bax. The SF following radiation was lower in the rAd-p53 transfected cells compared to the control cells, suggesting that rAd-p53 sensitizes SW1990 cells to radiation (D0 for the experimental and control groups was 2.199 and 2.462, respectively). 
Conclusions: Use of the adenoviral vector is an effective means of transfecting SW1990 cells with wild-type P53, and this sensitizes the cell line to irradiation. This work suggests that combining rAd-p53 with radiation therapy in pancreatic cancer may be therapeutically beneficial.},
	issn = {1993-0631},	url = {https://cjcr.amegroups.org/article/view/3076}
}