%A Huang Ting, Liao Hehe, Liu Xiaodong, Wang Ruoyu %T Study of signal transduction mechanisms of Xray induced multidrug resistance in nasopharyngeal squamous cell carcinoma CNE1 cells %0 Journal Article %D 2017 %J Journal of International Oncology %R 10.3760/cma.j.issn.1673-422X.2017.06.001 %P 401- %V 44 %N 6 %U {https://gjzlx.sdfmu.edu.cn/CN/abstract/article_10215.shtml} %8 2017-06-08 %X ObjectiveTo investigate the relationship between multidrug resistance of Xray irradiated human nasopharyngeal squamous carcinoma cell line CNE1 and platelet endothelial cell adhesion molecule1 (PECMA1)/phosphatidylinositol 3kinase (PI3K)/protein kinase B (AKT)/Bcl2 signaling pathway. Methods①The CNE1 cells were cultured in incubator. Exponentially growing CNE1 cells were exposed to 50 Gy ionizing radiation administered in 25 fractions, 2 Gy per fraction, once every two days, and the CNE1/R cells were collected. ②CNE1/R cells were cultured for 24 h, and divided into three groups: the control group, experimental group one (CNE1/R cells were processed through 1∶600 PECAM1 antibody for 24 h) and experimental group two (CNE1/R cells were processed through 10 μmol/L PI3K inhibitor LY294002 for 24 h). ③The half maximal inhibitory concentration (IC50) values of the control group and two experimental groups of CNE1/R cells were detected by methyl thiazolyl tetrazolium (MTT). ④The mRNA expressions of PI3K and Bcl2 in the control group and experimental group one were measured by semiquantitative reverse transcriptionpolymerase chain reaction (RTPCR). ⑤The mRNA expressions of AKT and Bcl2 in the control group and experimental group two were measured by semiquantitative RTPCR. Results①The IC50 of the control group, experimental group one and two were (2.99±0.02)μg/ml, (1.50±0.03)μg/ml and (1.60±0.05)μg/ml, and the difference among the three groups was statiatically signficant (F=4 381.263, P=0.000). The IC50 of the two experimental groups were obviously lower than that of the control group (t=116.885, P=0.000; t=73.006, P=0.000). ②The semiquantitative values of PI3K in the control group and experimental group one were 1.66±0.01 and 0.90±0.05 (t=50.394, P=0.000), and the semiquantitative values of Bcl2 were 1.66±0.02 and 0.71±0.05 (t=183.165, P=0.000), and the differences were statistically significant. ③The semiquantitative values of AKT of control group and experimental group two were 1.53±0.01 and 0.72±0.01 (t=135.281, P=0.000), and the semiquantitative values of Bcl2 were 1.66±0.02 and 0.63±0.02 (t=128.814, P=0.000), and the differences were statistically significant. ConclusionPECAM1 induced multidrug resistance of human nasopharyngeal squamous cell carcinoma CNE1 cells may be related to the activity of Bcl2 through the signal pathway of PI3K/AKT.