Ren Yuanyuan, Zhu Huadong, Han Song
Department of Oncology, People's Hospital of Taizhou, Taizhou, Jiangsu Province 225300, China.
Department of Oncology, Hospital 5, affiliated with Nantong University, Taizhou 225300, China.
Cancer Manag Res. 2020 Nov 2;12:11041-11050. doi: 10.2147/CMAR.S270087. eCollection 2020.
Non-small cell lung cancer (NSCLC) accounts for the majority of lung cancer cases, and effective treatment for this disease is still lacking. This study aimed to explore the potential role of LINC00518 and miR216b-5p on cell proliferation and tumor growth in NSCLC.
The expression of LINC00518, miR216b-5p, MMP7, and MMP9 in NSCLC cell lines was determined by RT-qPCR analysis, which was also used to confirm the transfection effects. After transfection, proliferation, clone-formation ability, migration, and invasion of NSCLC cells were detected by CCK8, clone-formation, wound-healing, and transwell assays, respectively. Western blot analysis was used to detect the expression of MMP7, MMP9, Ki67, and PCNA. A xenograft model was constructed by subcutaneous injection of transfected NSCLC cells into nude mice.
The results indicated that LINC00518 expression was increased and miR216b-5p expression decreased in NSCLC cell lines, and A549 cells were chosen for the next experiments. LINC00518 interference inhibited proliferation, invasion, and migration of A549 cells, together with the progression of NSCLC in vivo. In addition, LINC00518 directly targeted miR216b-5p. Downregulation of miR216b-5p weakened the inhibitory effect of LINC00518 interference on proliferation, invasion, and migration of A549 cells, as well as progression of NSCLC in vivo.
In conclusion, LINC00518 interference inhibits NSCLC, which is partially reversed by downregulation of miR216b-5p expression.
非小细胞肺癌(NSCLC)占肺癌病例的大多数,且仍缺乏针对该疾病的有效治疗方法。本研究旨在探讨LINC00518和miR216b - 5p在NSCLC细胞增殖和肿瘤生长中的潜在作用。
通过RT - qPCR分析确定NSCLC细胞系中LINC00518、miR216b - 5p、MMP7和MMP9的表达,该方法也用于确认转染效果。转染后,分别通过CCK8、克隆形成、伤口愈合和Transwell实验检测NSCLC细胞的增殖、克隆形成能力、迁移和侵袭。蛋白质免疫印迹分析用于检测MMP7、MMP9、Ki67和PCNA的表达。通过将转染后的NSCLC细胞皮下注射到裸鼠体内构建异种移植模型。
结果表明,NSCLC细胞系中LINC00518表达增加而miR216b - 5p表达降低,并选择A549细胞进行后续实验。LINC00518干扰抑制了A549细胞的增殖、侵袭和迁移,以及体内NSCLC的进展。此外,LINC00518直接靶向miR216b - 5p。miR216b - 5p下调减弱了LINC00518干扰对A549细胞增殖、侵袭和迁移的抑制作用,以及体内NSCLC的进展。
总之,LINC00518干扰抑制NSCLC,miR216b - 5p表达下调可部分逆转这种抑制作用。