Department of Pediatric Stomatology, Tianjin Stomatological Hospital, Tianjin, China.
Bioengineered. 2021 Dec;12(1):8724-8737. doi: 10.1080/21655979.2021.1978196.
Increasing evidence demonstrated long non-coding RNAs (lncRNAs) play important roles in the occurrence and development of oral squamous cell carcinoma (OSCC). This study aimed to explore the role and molecular mechanism of lncRNA HOXA-AS3 in the progression of OSCC. Here, we found that he expression of lncRNA HOXA-AS3 was upregulated in OSCC tissues and cell lines compared with the para-cancerous tissues and normal human oral keratinocyte (NHOK), respectively. Inhibition of HOXA-AS3 significantly inhibited the proliferation and colony formation of OSCC cells. Further, the luciferase reporter assay showed that HOXA-AS3 was directly bound to miR-218-5p. Moreover, the expression of miR-218-5p was negatively regulated by HOXA-AS3, and miR-218-5p could inhibit the expression of collagen type I alpha1 (COL1A1) and lysophosphatidylcholine acyltransferase 1 (LPCAT1). In addition, silencing miR-218-5p reversed the inhibitory effect of HOXA-AS3 knockdown on the proliferative potential of OSCC cells. In summary, our study illustrated that HOXA-AS3 promoted cancer cell proliferation in OSCC, possibly by sponging miR-218-5p for the first time, which provides a new target or a potential diagnostic biomarker for OSCC.
越来越多的证据表明,长链非编码 RNA(lncRNA)在口腔鳞状细胞癌(OSCC)的发生和发展中发挥重要作用。本研究旨在探讨 lncRNA HOXA-AS3 在 OSCC 进展中的作用和分子机制。在这里,我们发现与癌旁组织和正常人口腔角质细胞(NHOK)相比,lncRNA HOXA-AS3 在 OSCC 组织和细胞系中的表达上调。HOXA-AS3 的抑制显著抑制了 OSCC 细胞的增殖和集落形成。此外,荧光素酶报告基因检测显示 HOXA-AS3 可直接与 miR-218-5p 结合。此外,HOXA-AS3 负调控 miR-218-5p 的表达,miR-218-5p 可抑制胶原类型 I alpha1(COL1A1)和溶血磷脂酰胆碱酰基转移酶 1(LPCAT1)的表达。此外,沉默 miR-218-5p 逆转了 HOXA-AS3 敲低对 OSCC 细胞增殖潜能的抑制作用。总之,我们的研究首次表明,HOXA-AS3 通过海绵 miR-218-5p 促进 OSCC 中的癌细胞增殖,为 OSCC 提供了新的治疗靶点或潜在的诊断生物标志物。