Our study aimed to explore the effects of
long noncoding RNA (
lncRNA)-ANCR on the invasion and migration of
colorectal cancer (CRC) cells by regulating
enhancer of zeste homolog 2 (EZH2) expression. CRC tissues and adjacent normal tissues were collected and CRC SW620 cells line and normal human intestinal epithelial cells (HIECs) were incubated. CRC SW620 cells line was transfected with ANCR-
siRNA. The expressions of ANCR and EZH2
mRNA were measured by real-time quantitative polymerase chain reaction (RT-qPCR). EZH2 and trimethylation of H3K27 (H3K27me3)
protein expressions were detected using Western blotting. The relationship between ANCR and EZH2 was determined through
RNA pull-down and co-immunoprecipitation (co-IP) assays. Cell invasion and migration were determined by Trans-well and cell scratch assays. ANCR, EZH2 and H3K27me3 expressions were up-regulated in CRC tissues and SW620 cells (all P < 0.05). After transfected with ANCR-
siRNA, SW620 cells showed decreased ANCR expression and EZH2
mRNA and
protein expressions (all P < 0.05). According to the results of
RNA pull-down and co-IP assays, ANCR could specifically bind to EZH2. The results of Trans-well and cell scratch tests showed that when ANCR expression was decreased, the invasion and migration abilities of SW620 cells significantly declined (both P < 0.05). In conclusion, these results suggest that
lncRNA-ANCR could influence the invasion and migration of CRC cells by specifically binding to EZH2.