Che Hongze, Che Yanhai, Zhang Zhimin, Lu Qing
Department of Endodontics, Hospital of Stomatology, Jilin University, Changchun, China.
Department of Science and Education, Hospital of Stomatology, Jilin University, Changchun, China.
Front Oncol. 2021 Apr 21;11:657876. doi: 10.3389/fonc.2021.657876. eCollection 2021.
Recently, additional long noncoding RNAs (lncRNAs) have been identified and their possible roles were investigated in a variety of human tumors. One of these lncRNAs, LINC01929, promoted the progression of some cancers, whereas its expression and biological function in human oral squamous cell carcinoma (OSCC) remains still mostly uncertain. The LINC01929 expression in OSCC tissues or cell lines was identified quantitative real-time polymerase chain reaction. The cell counting kit-8, transwell migration, wound-healing, and flow cytometry assays were utilized to characterize the functions of LINC01929 in OSCC cells. The interactive relationships between LINC01929 and miR-137-3p, miR-137-3p and Forkhead box C1 (FOXC1) were investigated by the dual-luciferase activity assay. Our findings demonstrated that LINC01929 was highly expressed in OSCC tissue samples and cell lines, whereas miR-137-3p expression was downregulated. LINC01929 acted as a carcinogenic lncRNA with accelerated OSCC cell proliferation, migration and invasion, and suppression of apoptosis. We further indicated that LINC01929 facilitated tumor growth in xenograft mouse models. Mechanistically, LINC01929 acted as a sponge for miR-137-3p to elevate FOXC1 expression, which is the target of miR-137-3p. In addition, downregulated miR-137-3p expression rescued the suppressive behaviors of LINC01929 knockdown on the biological behaviors of OSCC cells. Taken together, LINC01929 functioned as a tumor-promoting lncRNA the miR-137-3p/FOXC1 axis in OSCC, suggesting novel targets for OSCC therapy.
最近,人们发现了更多的长链非编码RNA(lncRNA),并对其在多种人类肿瘤中的潜在作用进行了研究。这些lncRNA之一,即LINC01929,促进了某些癌症的进展,而其在人类口腔鳞状细胞癌(OSCC)中的表达和生物学功能仍大多未知。通过定量实时聚合酶链反应确定了OSCC组织或细胞系中LINC01929的表达。利用细胞计数试剂盒-8、Transwell迁移、伤口愈合和流式细胞术检测来表征LINC01929在OSCC细胞中的功能。通过双荧光素酶活性检测研究了LINC01929与miR-137-3p、miR-137-3p与叉头框C1(FOXC1)之间的相互作用关系。我们的研究结果表明,LINC01929在OSCC组织样本和细胞系中高表达,而miR-137-3p的表达下调。LINC01929作为一种致癌lncRNA,可加速OSCC细胞的增殖、迁移和侵袭,并抑制细胞凋亡。我们进一步表明,LINC01929促进了异种移植小鼠模型中的肿瘤生长。从机制上讲,LINC01929作为miR-137-3p的海绵,提高了miR-137-3p的靶标FOXC1的表达。此外,miR-137-3p表达下调挽救了LINC01929敲低对OSCC细胞生物学行为的抑制作用。综上所述,LINC01929在OSCC中作为一种促进肿瘤的lncRNA,通过miR-137-3p/FOXC1轴发挥作用,为OSCC治疗提供了新的靶点。