ALBERT

Description: A schematic model of the role of long noncoding RNA (lncRNA) MALAT1 in controlling the stemness of esophageal squamous cell carcinoma (ESCC). LncRNA MALAT1 directly binds to Yes‐associated protein (YAP), thereby enhancing YAP transcriptional activity, which in turn is responsible for the stemness of ESCC. The tumor promoting roles of long noncoding RNA (lncRNA) MALAT1 have been revealed in various cancers; however, its roles in esophageal squamous cell carcinoma (ESCC) have not previously been disclosed. In this study, we found that MALAT1 expression was remarkably increased in ESCC cells compared to normal human esophageal epithelial cells. In addition, knockdown of MALAT1 attenuated the stemness of ESCC cells, as evidenced by a decrease in spheroid formation capacity, stemness marker expression and aldehyde dehydrogenase 1 activity. Moreover, MALAT1 knockdown decreased the migration ability of ESCC cells. Notably, knockdown of MALAT1 enhanced the radiosensitivity and chemosensitivity of ESCC cells. We also established that MALAT1 binds directly to Yes‐associated protein (YAP), thereby enhancing YAP protein expression and increasing YAP transcriptional activity. Overexpression of YAP partially rescued the effect of MALAT1 knockdown on stemness and radiosensitivity of ESCC cells. Overall, this study has identified that a novel MALAT1–YAP axis promotes the stemness of ESCC cells, and thus could be a potential target for treatment of ESCC.