Chen Jie, Zhang Fan, Wang Junjun, Hu Lijuan, Chen Jian, Xu Gang, Wang Yumin
Department of Intensive Care Unit, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Department of Laboratory Medicine, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
J Cell Biochem. 2017 Oct;118(10):3102-3110. doi: 10.1002/jcb.26178. Epub 2017 Jun 22.
Previously, a significantly upregulated lncRNA, LINC01512, in lung adenocarcinoma (LAD) was obtained, while its biological function and molecular mechanisms were unclear. The expression level of LINC01512 was estimated by qPCR from 100 pairs of LAD and NT samples. The correlation of LINC01512 to clinical data of LAD patients was analyzed. LINC01512 was knocked down and overexpressed in SPCA-1 and A549 cell lines by lentivirus-mediated technology, and the oncological behavioral changes of SPCA-1 and A549 cells were observed, as well as, tumorigenicity in experimental nude mice. Compared to the adjacent tissues, LINC01512 was obviously upregulated in LAD. The expression level of LINC01512 was closely related to lymph node metastasis and tumor node metastasis (TNM) stage. Survival analysis showed that the survival time of high expression LINC01512 group was significantly shorter than the low-expression group in LAD. Knockdown or overexpression test unanimously confirmed that LINC01512 can increase the ability of cell migration, invasion, proliferation, colony formation, adhesion, and S phase and G2/M phase cells, whereas decrease the apoptosis and G0/G1 phase cells. Nude mice experiments confirmed that LINC01512 significantly enhanced the speed and weight of tumorigenicity. LINC01512 is an oncogenic lncRNA gene that promotes the progression and distinctly enhances the oncogenic ability in lung adenocarcinoma. J. Cell. Biochem. 118: 3102-3110, 2017. © 2017 The Authors. Journal of Cellular Biochemistry Published by Wiley Periodicals Inc.
此前,在肺腺癌(LAD)中获得了一种显著上调的长链非编码RNA(lncRNA)LINC01512,但其生物学功能和分子机制尚不清楚。通过qPCR从100对LAD和正常组织(NT)样本中评估LINC01512的表达水平。分析了LINC01512与LAD患者临床数据的相关性。通过慢病毒介导的技术在SPCA-1和A549细胞系中敲低和过表达LINC01512,观察SPCA-1和A549细胞的肿瘤行为变化以及在实验裸鼠中的致瘤性。与相邻组织相比,LINC01512在LAD中明显上调。LINC01512的表达水平与淋巴结转移和肿瘤-淋巴结-转移(TNM)分期密切相关。生存分析表明,LAD中LINC01512高表达组的生存时间明显短于低表达组。敲低或过表达试验一致证实,LINC01512可提高细胞迁移、侵袭、增殖、集落形成、黏附能力以及S期和G2/M期细胞比例,而降低细胞凋亡率和G0/G1期细胞比例。裸鼠实验证实,LINC01512显著增强了致瘤速度和肿瘤重量。LINC01512是一个致癌lncRNA基因,可促进肺腺癌进展并显著增强其致癌能力。《细胞生物化学杂志》118: 3102 - 3110, 2017。© 2017作者。《细胞生物化学杂志》由威利期刊公司出版