<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9</volume><submitter>Liu J</submitter><pubmed_abstract>&lt;b>Background:&lt;/b> The spliceosome plays an important role in mRNA alternative splicing and is aberrantly expressed in several tumors. However, the potential roles of spliceosome-related genes in the progression of hepatocellular carcinoma (HCC) remain poorly understood. &lt;b>Materials and Methods:&lt;/b> Patient data were acquired from public databases. Expression differences and survival analyses were used to assess the importance of spliceosome-related genes in HCC prognosis. To explore the potential regulatory mechanisms of these genes, a protein-protein interaction network was constructed and screened using univariate and multivariate Cox regression and random forest analyses. This was used to create a five-gene prognostic model. The prognostic value and predictive power of the five-gene signature were assessed using the Kaplan-Meier and time-dependent receiver operating characteristic analyses in the training set. These results were further validated in an independent external set. To facilitate clinical application, a nomogram was prepared to predict the overall survival of HCC patients. The relative expression of five genes was detected using real-time quantitative polymerase chain reaction. &lt;b>Results:&lt;/b> The analysis revealed that &lt;i>LSM1-7, SNRPB, SNRPD1-3, SNRPE, SNRPF, SNRPG,&lt;/i> and &lt;i>SNRPN&lt;/i> could be used as prognostic biomarkers in HCC patients. Moreover, the five-gene risk model could clearly distinguish between the high-and low-risk groups. Furthermore, the risk model was associated with the tumor mutation burden, immune cell infiltration of CD8&lt;sup>+&lt;/sup> T cells, natural killer T cells, M2 macrophages, and immune checkpoint inhibitors, which also demonstrated the predictive efficacy of this risk model in HCC immunotherapy. &lt;b>Conclusion:&lt;/b> Spliceosome-related genes and the five-gene signature could serve as novel prognostic biomarkers for HCC patients, aiding clinical patient monitoring and follow-up.</pubmed_abstract><journal>Frontiers in molecular biosciences</journal><pagination>759792</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8907852</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Determining the Prognostic Value of Spliceosome-Related Genes in Hepatocellular Carcinoma Patients.</pubmed_title><pmcid>PMC8907852</pmcid><pubmed_authors>Li W</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Zhang D</pubmed_authors><pubmed_authors>Gu L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Determining the Prognostic Value of Spliceosome-Related Genes in Hepatocellular Carcinoma Patients.</name><description>&lt;b>Background:&lt;/b> The spliceosome plays an important role in mRNA alternative splicing and is aberrantly expressed in several tumors. However, the potential roles of spliceosome-related genes in the progression of hepatocellular carcinoma (HCC) remain poorly understood. &lt;b>Materials and Methods:&lt;/b> Patient data were acquired from public databases. Expression differences and survival analyses were used to assess the importance of spliceosome-related genes in HCC prognosis. To explore the potential regulatory mechanisms of these genes, a protein-protein interaction network was constructed and screened using univariate and multivariate Cox regression and random forest analyses. This was used to create a five-gene prognostic model. The prognostic value and predictive power of the five-gene signature were assessed using the Kaplan-Meier and time-dependent receiver operating characteristic analyses in the training set. These results were further validated in an independent external set. To facilitate clinical application, a nomogram was prepared to predict the overall survival of HCC patients. The relative expression of five genes was detected using real-time quantitative polymerase chain reaction. &lt;b>Results:&lt;/b> The analysis revealed that &lt;i>LSM1-7, SNRPB, SNRPD1-3, SNRPE, SNRPF, SNRPG,&lt;/i> and &lt;i>SNRPN&lt;/i> could be used as prognostic biomarkers in HCC patients. Moreover, the five-gene risk model could clearly distinguish between the high-and low-risk groups. Furthermore, the risk model was associated with the tumor mutation burden, immune cell infiltration of CD8&lt;sup>+&lt;/sup> T cells, natural killer T cells, M2 macrophages, and immune checkpoint inhibitors, which also demonstrated the predictive efficacy of this risk model in HCC immunotherapy. &lt;b>Conclusion:&lt;/b> Spliceosome-related genes and the five-gene signature could serve as novel prognostic biomarkers for HCC patients, aiding clinical patient monitoring and follow-up.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-19T03:11:19.739Z</modification><creation>2025-04-04T07:56:04.865Z</creation></dates><accession>S-EPMC8907852</accession><cross_references><pubmed>35281269</pubmed><doi>10.3389/fmolb.2022.759792</doi></cross_references></HashMap>