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Please use this identifier to cite or link to this item: http://142.54.178.187:9060/xmlui/handle/123456789/16228
Title: Research on chemotherapy efficacy of twist gene on cervical cancer cells to paclitaxel
Authors: Sun, Zhenchang
Zhang, Dan
Cui, Yingying
Cheng, Liangxing
Cao, Jingyu
Wu, Xiaolong
Keywords: Paclitaxel
cell growth inhibition rates
Caski cells
silent Twist gene
Issue Date: 22-Sep-2014
Publisher: Karachi: Faculty of Pharmacy & Pharmaceutical Sciences University of Karachi
Citation: Sun, Z., Zhang, D., Cui, Y., Cheng, L., Cao, J., & Wu, X. (2014). Research on chemotherapy efficacy of twist gene on cervical cancer cells to paclitaxel. Pakistan Journal of Pharmaceutical Sciences, 27(5).
Abstract: The silent Twist gene may increase the sensitivity of cervical cancer cells chemotherapy to paclitaxel, thus was a new idea to improve the efficacy of cancer chemotherapy. The aim was to explore chemotherapy sensitivity of silent Twist gene increased cervical cancer cells to paclitaxel through study the proliferation and apoptosis of cervical cancer Twist gene after paclitaxel treatment. Cervical carcinoma Caski cells and Hela cells was cultured in vitro, mRNA gene expression was detected by using semi-quantitative, fluorescence quantitative PCR, and transferred to Caski cells transiently, and affected with paclitaxel solution of five kinds of different concentrations of 0.001, 0.01, 0.1, 1, 10 umol/L respectively. Then the results of <0.05). Every 12h after 36h, the expression inhibition rate in two groups of Caski cells that has transfected this study was Twist gene expression in Caski cells was higher than in Hela cells, which was of significant difference (p siRNA1 and siRNA2 were 20.3%, 38.2%, 33%, 24%, 68.6%, 50.8% respectively. After 48h in five different concentrations of paclitaxel effect, the cell growth inhibition rate of group siRNA2 with the best transfection efficiency was obviously higher than that of negative control group and blank control group, and the growth inhibition rates showed concentration dependence (p<0.05). It can be concluded that Twist gene in Caski cell was of high expression and the silent Twist gene could inhibit Caski cell proliferation and promote its apoptosis, thus to improve the chemotherapy sensitivity of Caski cells.
URI: http://142.54.178.187:9060/xmlui/handle/123456789/16228
ISSN: 1011-601X
Appears in Collections:Issue No.5 (Supplementary)

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