Abstract：Objective: To investigate enhancement of silencing BRM gene by siRNA on the sensitivity of human pancreatic cancer cell line to gemcitabine. Methods: Panc-1 cells from human pancreatic cancer in vitro were cultured. Negative control NC and BRM siRNA were transfected into Panc-1 cells cultured in vitro. The expression of BRM in Panc-1 cells was detected by RT-PCR and Western Blot, so as to identify the silencing effect of BRM-specific siRNA. Different concentrations of gemcitabine were used to detect the cell proliferation rate, and the half-inhibitory concentration (IC50) was calculated. The apoptosis rate of Panc-1 cells and the protein expression levels of JAK2, STAT3, p-STAT3 and Survivin in Panc-1 cells were detected. Results: The expression of BRM mRNA and protein in Panc-1 cells of BRM siRNA group was significantly lower than that of blank control group and NC control group (P＜0.05). The inhibition rate of gemcitabine on Panc-1 cell proliferation in BRM siRNA group was higher than that in blank control group and NC control group (P＜0.05); The IC50 of the blank control group, the NC control group and the BRM siRNA group were 5.18 ug/mL, 5.05 ug/mL and 3.05 ug/mL, respectively; After gemcitabine treatment with the final concentration of 3.0ug/mL, the apoptotic rate of Panc-1 cells in BRM siRNA group was significantly higher than that in blank control group and NC control group (P＜0.05), STAT3 was not significantly changed (P＞0.05), while the expression of JAK2, p-STAT3 and Survivin protein was significantly decreased (P＜0.05). Conclusion: Silencing BRM expression by siRNA can increase the sensitivity of Panc-1 cells to citrate, which may be related to the activation of JAK2/STAT3 pathway by BRM to promote pancreatic cancer growth and drug resistance.
屈涛, 张弘刚, 汤海舰, 刘伟. siRNA沉默BRM增强胰腺癌细胞对吉西他滨敏感性的作用机制研究[J]. 河北医学, 2019, 25(10): 1620-1623.
QU Tao, ZHANG Honggang, et al. Study on the Mechanism of siRNA Silencing BRM Enhancing the Sensitivity of Pancreatic Cancer Cells to Gemcitabine. HeBei Med, 2019, 25(10): 1620-1623.
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2019, Vol. 25 
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