Objective To investigate the effects of lncRNA MAFG-AS1 and miR-143-3p on proliferation and apoptosis of cervical cancer cells and its potential mechanism. Methods After MAFG-AS1 and miR-143-3p expression vectors were transfected into Hela cells,qRT-PCR was used to detect the expression of miR-143-3p and MAFG-AS1 mRNA in Hela cells; protein expression,cell proli-feration activity and apoptosis were detected by Western blot, MTT assay and flow cytometry, respectively;dual-luciferase reporter gene was used to the interaction between lncRNA MAFG-AS1 and miR-143-3p. Results Compared with adjacent normal tissues,MAFG-AS1 mRNA expression was increased in cervical cancer tissues (0.905±0.115 vs 2.835±0.164,t=43.091,P<0.001),and miR-143-3p expression level was decreased (0.944±0.075 vs 0.382±0.071,t=24.336,P<0.001). Compared with the normal cervical cell line Ect1/E6E7,the expression of MAFG-AS1 mRNA in Hela cells was significantly increased(P<0.001),and the expression of miR-143-3p was significantly decreased(P<0.001). Down-regulation of MAFG-AS1 and miR-143-3p overexpression inhibited the proliferation of Hela cells and promoted apoptosis, inhibited the expression of Bcl-2 and Cyclin D1 proteins,and promoted the expression of Bax,Caspase-3,p21,and p27 proteins. MAFG-AS1 targeted to regulate the expression of miR-143-3p. Inhibition of miR-143-3p expression reversed the effect of MAFG-AS1 on inhibiting proliferation and promoting apoptosis Hela cells. Conclusions lncRNA MAFG-AS1 can inhibit the proliferation of cervical cancer cells and promote their apoptosis. The mechanism may be related to miR-143-3p,which will provide new targets for the prevention and treatment of cervical cancer.