Yang Si-Jia, Weng Jia-Lu, Wei Bin, Du Xue-Kui
Department of Respiratory Medicine, Ningbo No.2 Hospital, No. 41, Northwestern Street, Ningbo, Zhejiang Province, 315099, China.
Department of ophthalmology and otorhinolaryngology, Ningbo No.2 Hospital, No. 41, Northwestern Street, Ningbo, Zhejiang Province, 315099, China.
Open Life Sci. 2019 Dec 31;14:201-207. doi: 10.1515/biol-2019-0022. eCollection 2019 Jan.
To investigate how long non-coding RNAs DUXAP8 (LncRNA DUXAP8) influence the cell proliferation and invasion of non-small-cell lung cancer (NSCLC), we detected the expression levels of LncRNA DUXAP8 in lung cancer (LC) tissues, 4 LC-related cell lines (A549, SPC-A1, SK-MES-1 and NCI-H1299) and normal lung tissues via quantitative real-time PCR (qRT-PCR). Compared with normal lung tissue, LncRNA DUXAP8 was significantly up-regulated in NSCLC, especially in stage III / IV and diameter ≥ 3cm of lung cancer. Among 4 lung cancer cell lines, LncRNA DUXAP8 in A549 cells was the highest (<0.001). Construction of LncRNA DUXAP8 overexpression and LncRNA DUXAP8 knockout in A549 cell lines was further performed and subsequently injected into nude mice to build an in vivo tumor xenograft model. The results indicated that LncRNA DUXAP8 overexpression significantly promoted the A549 cells' proliferation, enhanced invasion and induced tumor growth. Conversely, LncRNA DUXAP8 knockout significantly suppressed A549 cells' proliferation, weakened invasion and inhibited tumor growth. Taken together, our results imply that LncRNA DUXAP8 is a potential regulatory molecular marker in non-small-cell lung cancer.
为了研究长链非编码RNA DUXAP8(LncRNA DUXAP8)对非小细胞肺癌(NSCLC)细胞增殖和侵袭的影响持续多久,我们通过定量实时PCR(qRT-PCR)检测了肺癌(LC)组织、4种与LC相关的细胞系(A549、SPC-A1、SK-MES-1和NCI-H1299)以及正常肺组织中LncRNA DUXAP8的表达水平。与正常肺组织相比,LncRNA DUXAP8在NSCLC中显著上调,尤其是在III/IV期和直径≥3cm的肺癌中。在4种肺癌细胞系中,A549细胞中的LncRNA DUXAP8最高(<0.001)。进一步构建了A549细胞系中LncRNA DUXAP8过表达和LncRNA DUXAP8敲除模型,随后将其注射到裸鼠体内以建立体内肿瘤异种移植模型。结果表明,LncRNA DUXAP8过表达显著促进了A549细胞的增殖,增强了侵袭能力并诱导了肿瘤生长。相反,LncRNA DUXAP8敲除显著抑制了A549细胞的增殖,减弱了侵袭能力并抑制了肿瘤生长。综上所述,我们的结果表明LncRNA DUXAP8是非小细胞肺癌中一种潜在的调控分子标志物。