LncRNA HOXC-AS3 increases non-small cell lung cancer cell migration and invasion by sponging premature miR-96

被引:9
|
作者
Wan, Li [1 ]
Cheng, Zaixing [1 ]
Sun, Quanchao [1 ]
Jiang, Ke [1 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Thorac Surg, Wuhan 43000, Hubei, Peoples R China
关键词
Non-small cell lung cancer; HOXC-AS3; miR-96; maturation; cell cycle; NONCODING RNAS; TARGETED THERAPY; STAGE IV; PROGNOSIS;
D O I
10.1080/17476348.2022.2030223
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background Long noncoding RNA (lncRNA) HOXC cluster antisense RNA 3 (HOXC-AS3) has been involved in breast cancer and gastric cancer, while its role in non-small cell lung cancer (NSCLC) is unknown. Methods The expression of HOXC-AS3 and miR-96 (both mature and premature) were detected using RT-qPCR. Nuclear fractionation assay and RNA pull-down assay were performed to detect the subcellular location of HOXC-AS3 and potential interaction with premature miR-96, respectively. Overexpression assays were performed to determine the role of HOXC-AS3 in the maturation of miR-96. Transwell assays were performed to explore the role of HOXC-AS3 and miR-96 in NSCLC cell invasion and migration. Results NSCLC tissues exhibited significantly increased expression levels of HOXC-AS3 and premature miR-96. HOXC-AS3 was localized to both nucleus and cytoplasm, and a direct interaction between HOXC-AS3 and premature miR-96 was observed. In NSCLC cells, HOXC-AS3 upregulated the expression of premature miR-96 but downregulated the expression of mature miR-96. Moreover, HOXC-AS3 suppressed the role of miR-96 in inhibiting NSCLC cell invasion and migration. Conclusion HOXC-AS3 may increase NSCLC cell growth and invasion by sponging premature miR-96 to suppress its maturation.
引用
收藏
页码:587 / 593
页数:7
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