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    					| Expression and Significance of miR-125b in Ovarian Cancer Cells | 
  					 
  					  										
						| GU Cai-ru, LIU Wei, LIN Meng-yuan | 
					 
															
						| Department of Gynecology, Guangzhou Red Cross Hospital, Jinan University, Guangzhou, Guangdong 510220, China | 
					 
										
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													     		                            						                            																	    Abstract  【Objective】  To investigate the effect and mechanism of miR-125b on energy metabolism and proliferation in ovarian cancer cells. 【Methods】  Real-time PCR was used to detect the expression level of miR-125b in human ovarian epithelial cells and ovarian cancer cells. The proliferation of ovarian cancer cells was recorded by CCK-8. Glucose uptake and lactic acid production in ovarian cancer cells were measured by 3H labeled 2-deoxyglucose (3H-2DG) method and lactic acid quantitative kit. Western blot was performed for the expression of hexokinase 2 (HK2) in ovarian cancer cells after miR-125b-mimics overexpression. 【Results】  The real time PCR results showed that the expression level of miR-125b in ovarian cancer cells was significantly lower than that in normal ovarian epithelial cells (P<0.05). The CCK-8 results demonstrated  that the proliferation capacity of ovarian cancer cells was significantly reduced after transfected with miR-125b-mimics for 48h and 72h compared with the control group (P<0.05). The quantitative results of 3H-2DG and lactic acid showed that glucose intake and lactic acid production were significantly reduced after overexpression of miR-125b in ovarian cancer cells (P<0.05); and aerobic glycolysis was significantly inhibited. Western blot results showed that the expression level of HK2 protein decreased after overexpression of miR-125b in ovarian cancer cells (P<0.05). 【Conclusion】  The low expression of miR-125b  in ovarian cancer cells  inhibits the energy metabolism and proliferation of ovarian cancer cells by down-regulating the expression of HK2.
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															    																	Received: 15 June 2020
																	    
															    															    															   	
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