Department of Biostatistics, College of Science, City University of Hong Kong, Hong Kong, China.
School of Nursing, Guangzhou Medical University, Guangzhou, Guangdong, China.
Ann Med. 2024 Dec;56(1):2408463. doi: 10.1080/07853890.2024.2408463. Epub 2024 Sep 28.
This study combined the bioinformatics and experiment-related technologies to analyze the impact of steroid 5 alpha-reductase 3 (SRD5A3) on the prognosis and immune microenvironment of Liver Hepatocellular Carcinoma (LIHC).
Gene expression and clinical data were obtained from public databases. The prognosis was evaluated using survival, multifactor Cox, enrichment, and mutation analyses. This was then verified through experiments.
The expression level of in LIHC tissues was significantly higher than that in the adjacent tissues. Kaplan-Meier survival analysis showed that high expression was associated with poor overall survival (OS) and short progression-free survival in patients with LIHC. Multivariate Cox regression analysis revealed that positive expression was an independent risk factor for OS in patients with LIHC. Expression of was negatively correlated with immune cell infiltration of CD4+ T, CD8+ T, and B cells. GO and KEGG enrichment analyses showed that was significantly enriched in signaling- and tumor metastasis-related pathways. Nomogram and calibration curve showed that the predicted performance of the model was consistent with the actual results. results confirmed that knockdown inhibited the migration, invasion, and proliferation of LIHC cells.
is actively expressed in LIHC, and positive expression of is an independent risk factor for different prognoses in patients with LIHC. can promote the proliferation, migration, and invasion of liver cancer cells and is related to short immune infiltration in patients with LIHC.
本研究结合生物信息学和实验相关技术,分析类固醇 5α-还原酶 3(SRD5A3)对肝细胞肝癌(LIHC)预后和免疫微环境的影响。
从公共数据库中获取基因表达和临床数据。使用生存、多因素 Cox、富集和突变分析评估预后。然后通过实验进行验证。
在 LIHC 组织中的表达水平明显高于相邻组织。Kaplan-Meier 生存分析表明,高表达与 LIHC 患者的总生存期(OS)和无进展生存期短相关。多因素 Cox 回归分析显示,阳性表达是 LIHC 患者 OS 的独立危险因素。表达与 CD4+T、CD8+T 和 B 细胞的免疫细胞浸润呈负相关。GO 和 KEGG 富集分析表明,与信号转导和肿瘤转移相关途径显著富集。列线图和校准曲线表明,模型的预测性能与实际结果一致。实验结果证实,下调抑制 LIHC 细胞的迁移、侵袭和增殖。
在 LIHC 中呈高表达,阳性表达是 LIHC 患者不同预后的独立危险因素。可促进肝癌细胞的增殖、迁移和侵袭,并与 LIHC 患者免疫浸润时间短有关。