Srisathaporn Sawarot, Pientong Chamsai, Heawchaiyaphum Chukkris, Nukpook Thawaree, Aromseree Sirinart, Ekalaksananan Tipaya
Department of Microbiology, Faculty of Medicine, Khon Kaen University, Khon Kaen 40002, Thailand.
HPV & EBV and Carcinogenesis Research Group, Khon Kaen University, Khon Kaen 40002, Thailand.
Int J Mol Sci. 2024 Nov 22;25(23):12565. doi: 10.3390/ijms252312565.
Dysregulated long non-coding RNA (lncRNA) expression is linked to various cancers and may be influenced by oncogenic Epstein-Barr virus (EBV) infection, a known and detectable risk factor in oral squamous cell carcinoma (OSCC) patients. However, research on the oncogenic role of EBV-induced lncRNAs in OSCC is limited. To identify lncRNA-associated EBV infection and OSCC carcinogenesis, the differential expression of RNA-seq datasets from paired normal adjacent and OSCC tissues, and microarray data from EBV-negative and EBV-positive SCC25 cells, were identified and selected, respectively, for interaction, functional analysis, and CCK-8 cell proliferation, wound healing, and invasion Transwell assays. In OSCC tissues, 6731 differentially expressed lncRNAs were identified when compared to normal tissues from RNA-seq datasets, with 295 linked to EBV-induced OSCC carcinogenesis from microarray datasets. The EBV-induced lncRNA showed significant upregulation in EBV-positive SCC25 cells and EBV-infected adjacent and OSCC tissue samples. potentially promotes OSCC via the lncRNA-miRNA-mRNA axis or direct protein interactions, affecting various cellular processes. Studies in OSCC cell lines revealed that elevated levels enhanced cell migration and invasion. This study demonstrates 's contribution to tumor progression and possible interactions with its targets in OSCC, offering insights for future research on functional mechanisms and therapeutic targets in EBV-associated OSCC.
长链非编码RNA(lncRNA)表达失调与多种癌症相关,并且可能受致癌性爱泼斯坦-巴尔病毒(EBV)感染影响,EBV感染是口腔鳞状细胞癌(OSCC)患者已知且可检测到的危险因素。然而,关于EBV诱导的lncRNAs在OSCC中的致癌作用的研究有限。为了确定lncRNA相关的EBV感染和OSCC致癌作用,分别从配对的正常相邻组织和OSCC组织的RNA-seq数据集中筛选差异表达,以及从EBV阴性和EBV阳性的SCC25细胞的微阵列数据中筛选差异表达,用于相互作用、功能分析以及CCK-8细胞增殖、伤口愈合和侵袭Transwell实验。在OSCC组织中,与RNA-seq数据集中的正常组织相比,鉴定出6731个差异表达的lncRNAs,其中295个与微阵列数据集中EBV诱导的OSCC致癌作用相关。EBV诱导的lncRNA在EBV阳性的SCC25细胞以及EBV感染的相邻和OSCC组织样本中显著上调。其可能通过lncRNA- miRNA- mRNA轴或直接的蛋白质相互作用促进OSCC,影响各种细胞过程。在OSCC细胞系中的研究表明,水平升高会增强细胞迁移和侵袭。这项研究证明了其对肿瘤进展的作用以及在OSCC中与其靶标的可能相互作用,为未来关于EBV相关OSCC的功能机制和治疗靶点的研究提供了见解。