首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Expression profile analysis identifies the long non-coding RNA landscape and the potential carcinogenic functions of LINC00668 in laryngeal squamous cell carcinoma
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Expression profile analysis identifies the long non-coding RNA landscape and the potential carcinogenic functions of LINC00668 in laryngeal squamous cell carcinoma

机译:表达谱分析鉴定了LINC00668在喉鳞状细胞癌中长的非编码RNA景观和潜在的致癌功能

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In order to explore the differentially expressed long non-coding RNAs (lncRNAs) in laryngeal squamous cell carcinoma (LSCC), the GSE84957 lncRNA expression profile was included in the present study through data mining in the National Center for Biotechnology Information/Gene Expression Omnibus (NCBI/GEO). Then, the differentially expressed genes (DEGs) of LSCC (1646 lncRNAs and 2713 mRNAs, fold change = 2, P = 0.05) were identified from the GSE84957 dataset using bioinformatics analysis. Of the 10 selected differentially expressed lncRNAs, the expression of 7 IncRNAs were verified by qRT-PCR method. Then, LINC00668, a potential carcinogenic IncRNA, was screened out by narrowing down the screening criteria (fold change = 4, P = 0.01). Furthermore, correlation analysis demonstrated that expression levels of LINC00668 were associated with age, pathological differentiation degree, T stage, clinical stage and cervical lymph node metastasis. Moreover, a series of bioinformatics tools and in vitro experiments proved that knockdown of LINC00668 inhibited the proliferation, migration and invasion ability of LSCC cells. The present study identified the lncRNAs landscape of LSCC through data mining and bioinformatics analysis, and verified oncogenic LINC00668, which may play important roles in promoting LSCC cells proliferation, migration and invasion.
机译:为了探讨喉鳞状细胞癌(LSCC)中的差异表达的长期非编码RNA(LNCRNA),GSE84957 LNCRNA表达谱通过在国家生物技术信息/基因表达综合症中心中的数据挖掘中包括在本研究中( ncbi / geo)。然后,使用生物信息学分析,从GSE84957数据集中鉴定LSCC(1646LNCRNA和2713mRNA,折叠变化& = 2,P = 0.05)的差异表达基因在所选的差异表达的LNCRNA中,通过QRT-PCR方法验证了7个IncrNA的表达。然后,通过缩小筛选标准(折叠变化= 4,p = 0.01),筛选出筛选潜在的致癌IncRNA。此外,相关性分析表明,LINC00668的表达水平与年龄,病理分化度,T阶段,临床阶段和宫颈淋巴结转移相关。此外,一系列生物信息学工具和体外实验证明了LINC00668的敲低抑制LSCC细胞的增殖,迁移和侵袭能力。本研究通过数据挖掘和生物信息学分析鉴定了LSCC的LNCRNA景观,并验证了致癌物质00668,这可能在促进LSCC细胞增殖,迁移和侵袭方面发挥重要作用。

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