Effect of JIP on the proliferation and apoptosis of nasopharyngeal carcinoma cells

Background Objective: Previous studies showed that JNK signaling pathway activated by LMP1 plays an important role in carcinogenesis of nasopharyngeal carcinoma (NPC). JNK interacting protein (JIP) can inhibit JNK signaling pathway in NPC cell. This study was designed to elucidate the effect of JIP on the proliferation and apoptosis of NPC cells. Methods: After treatment with JIP at different concentrations and time points, the number of proliferating cells were determined by MTT assay; the ability of proliferation of NPC cells was measured by the rate of cloning formation; cell cycle and the apoptotic rate of NPC cells was assayed by flow cytometry. Results: 1MTT assay showed that cell proliferation was significantly inhibited by JIP in a dose and time dependent manner.After treatment with JIP for 24,48,and 72 hours, the rate of survival cells were 77.8%,59.2%, and 61.8%, respectively. 2The number and volume of colonies were decreased after transfection with JIP. 3The number of cells in S phase was decreased from 25.87% to 19.96%, and the number of cells in G0/G1 phase was elevated from 66.24% to 71.89% after treatment with JIP. 4In contrast to the control group,the 24 hours apoptotic rate was elevated from 1.25% to 8.25%(about 6.6 times);the 48 hours apoptotic rate was elevated from 1.04% to 31.45%(about 30 times).Conclusions: The results demonstrated that JIP inhibit the growth of nasopharyngeal carcinoma through arresting the cell cycle at G1/S checkpoint and triggering the apoptosis of cells. Data suggest that JIP is a potent molecular drug for the treatmeat of the patients with nasopharyngeal carcinoma.