Fig. 1

CTBP1-AS2 is aberrantly up-regulated in CC cells. a qRT-PCR assay was used to examine CTBP1-AS2 expression in CC cell lines and normal cell line. b The transfection efficiency of sh-CTBP1-AS2#1/2 plasmid was guaranteed by qRT-PCR. c, d CCK-8 and EdU were performed to detect cell proliferation. e TUNEL was used to examine apoptosis. f, g Transwell assays were conducted to measure cell migration and invasion ability respectively. h Western blot was performed to examine the expression of apoptosis-related proteins. ^*P < 0.05, ^**P < 0.01