Han Xu, Xu Zixiao, Tian Gang, Tang Zhen, Gao JianYong, Wei Yibo, Xu XiaoGang
Department of Stomatology, Changhai Hospital Affiliated to Second Military Medical University, Shanghai, China.
Arch Med Sci. 2019 Jul;15(4):992-1000. doi: 10.5114/aoms.2018.73343. Epub 2018 Mar 2.
Aberrant expression of long non-coding RNAs (lncRNAs) is associated with metastasis and poor prognosis in patients with various cancer types. However, few studies have assessed lncRNAs in oral squamous cell carcinoma (OSCC). This study aimed to investigate the expression and impact of lncRNAs in OSCC.
Real-time PCR analysis was used to examine the expression of four lncRNAs, MALAT-1, UCA1, BC200 and SRA, in 14 OSCC and adjacent normal tissue pairs. The impact of MALAT-1 suppression by siRNA on the proliferation, apoptosis, anchorage-independent growth and migration of the human tongue carcinoma cell line SSC4 was also determined.
MALAT-1 levels were significantly higher in the OSCC tissue than in the normal tissues ( < 0.004); no significant differences in UCA1, BC200 or SRA RNA levels were observed. Knockdown of MALAT-1 by siRNA significantly suppressed proliferation of SSC4 cells ( < 0.004) and enhanced their apoptosis ( < 0.001). In addition, siRNA-mediated suppression of MALAT-1 inhibited SSC4 cell colony formation ( < 0.001) and migration ( < 0.004).
Elevated expression of MALAT-1 in OSCC may play a role in tumorigenesis and/or metastasis. Further studies are necessary to identify the mechanism by which MALAT-1 influences SCC4 growth and migration and validate its increased expression in OSCC patients.
长链非编码RNA(lncRNAs)的异常表达与多种癌症类型患者的转移及不良预后相关。然而,很少有研究评估口腔鳞状细胞癌(OSCC)中的lncRNAs。本研究旨在调查lncRNAs在OSCC中的表达及影响。
采用实时PCR分析检测14对OSCC组织及其相邻正常组织中4种lncRNAs,即MALAT-1、UCA1、BC200和SRA的表达。还确定了siRNA抑制MALAT-1对人舌癌细胞系SSC4增殖、凋亡、非锚定依赖性生长和迁移的影响。
OSCC组织中MALAT-1水平显著高于正常组织(<0.004);未观察到UCA1、BC200或SRA RNA水平有显著差异。siRNA敲低MALAT-1可显著抑制SSC4细胞的增殖(<0.004)并增强其凋亡(<0.001)。此外,siRNA介导的MALAT-1抑制可抑制SSC4细胞集落形成(<0.001)和迁移(<0.004)。
OSCC中MALAT-1表达升高可能在肿瘤发生和/或转移中起作用。有必要进一步研究以确定MALAT-1影响SCC4生长和迁移的机制,并验证其在OSCC患者中表达增加的情况。