Lu Jing, Cao Wanyue, He Zeping, Wang Haoyu, Hao Jialing, Xu Junming
Department of General Surgery, Shanghai General Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai 200080, China.
J Oncol. 2022 Aug 29;2022:3090523. doi: 10.1155/2022/3090523. eCollection 2022.
Long noncoding RNAs (lncRNAs) are found to be novel biomarkers for hepatocellular carcinoma (HCC) and play an important role in tumor progression. We established a genomic instability-related long noncoding RNA signature (GIlncSig) as an independent prognosis factor and also investigated its impact on prognosis significance.
Somatic mutation profiles, clinical characteristics, and RNA sequencing data were obtained from The Cancer Genome Atlas (TCGA) database. Lasso regression was used to construct GIlncSig. KEGG was used to identify the possible biological pathways. ESTIMATE and CIBERSORT algorithms were used to calculate the immune microenvironment scores and proportion of immune cells in HCC patients. The expression of LINC00501 was conducted by qRT-PCR. Cell proliferation was measured by EdU, CCK-8, and colony formation assay, and cell migration and invasion ability were measured by wound healing and transwell assay.
135 genomic instability-related lncRNAs were identified, and GIlncSig was constructed using 13 independent lncRNAs with significant prognosis values. Based on the GIlncSig, high-risk group had worse clinical outcomes than low-risk group, while high-risk group also had higher UBQLN4, KRAS, ARID1A, and PIK3CA expression. Moreover, the efficiency of GIlncSig combining single-gene mutation was higher than single-gene mutation alone such as TP53. The results of CIBERSORT and ESTIMATE showed that GS group and GU group had significantly different immune infiltration. In addition, LINC00501 was identified as a potential biomarker in HCC with strong relationship with clinical characteristics. In vitro assays validated that LINC00501 promoted proliferation and migration of HCC cell lines.
Our results showed that GIlncSig serves as a potential independent prognosis factor to predict HCC patients' prognosis for exploring potential mechanism and therapy strategy. Besides, LINC00501 plays an important role in the progression of HCC, which may be a potential therapy target.
长链非编码RNA(lncRNAs)被发现是肝细胞癌(HCC)的新型生物标志物,并在肿瘤进展中发挥重要作用。我们建立了一种与基因组不稳定性相关的长链非编码RNA特征(GIlncSig)作为独立的预后因素,并研究了其对预后意义的影响。
从癌症基因组图谱(TCGA)数据库中获取体细胞突变谱、临床特征和RNA测序数据。使用套索回归构建GIlncSig。使用KEGG鉴定可能的生物学途径。使用ESTIMATE和CIBERSORT算法计算HCC患者的免疫微环境评分和免疫细胞比例。通过qRT-PCR检测LINC00501的表达。通过EdU、CCK-8和集落形成试验测量细胞增殖,通过伤口愈合和Transwell试验测量细胞迁移和侵袭能力。
鉴定出135个与基因组不稳定性相关的lncRNAs,并使用13个具有显著预后价值的独立lncRNAs构建了GIlncSig。基于GIlncSig,高危组的临床结局比低危组差,而高危组的UBQLN4、KRAS、ARID1A和PIK3CA表达也更高。此外,GIlncSig结合单基因突变的效率高于单独的单基因突变,如TP53。CIBERSORT和ESTIMATE的结果表明,GS组和GU组的免疫浸润存在显著差异。此外,LINC00501被鉴定为HCC中的潜在生物标志物,与临床特征密切相关。体外试验验证了LINC00501促进HCC细胞系的增殖和迁移。
我们的结果表明,GIlncSig作为一种潜在的独立预后因素,可用于预测HCC患者的预后,以探索潜在机制和治疗策略。此外,LINC00501在HCC进展中起重要作用,可能是一个潜在的治疗靶点。