<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Xu YJ</submitter><funding>Key Technologies Research and Development Program</funding><funding>National Major Science and Technology Projects of China</funding><funding>National Natural Science Foundation of China</funding><funding>Guangdong Key Laboratory of Innovation Method and Decision Management System</funding><pagination>610</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8600893</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>The accumulation of single nucleotide variants (SNVs) and the emergence of neoantigens can affect tumour proliferation and the immune microenvironment. However, the SNV-related immune microenvironment characteristics and key genes involved in hepatocellular carcinoma (HCC) are still unclear. We aimed to evaluate differences in the SNV-related immune microenvironment, construct a prognostic model and validate the key genes in vitro.&lt;h4>Methods&lt;/h4>The categories of samples were defined by the expression of SNV score-related genes to evaluate the differences in mutational features, immune environment and prognosis. The survival model was constructed with survival-associated genes and verified in two independent test datasets. RCAN2, the key gene screened out for biofunctio</pubmed_abstract><journal>Cancer cell international</journal><pubmed_title>Construction of a single nucleotide variant score-related gene-based prognostic model in hepatocellular carcinoma: analysis of multi-independent databases and validation in vitro.</pubmed_title><pmcid>PMC8600893</pmcid><funding_grant_id>2019B110233002</funding_grant_id><funding_grant_id>No. 81625017</funding_grant_id><funding_grant_id>2017YFA0505803</funding_grant_id><funding_grant_id>No. 82072610</funding_grant_id><funding_grant_id>2018ZX10302205</funding_grant_id><pubmed_authors>Shi M</pubmed_authors><pubmed_authors>He MK</pubmed_authors><pubmed_authors>Kan A</pubmed_authors><pubmed_authors>Xu YJ</pubmed_authors><pubmed_authors>Bu XY</pubmed_authors><pubmed_authors>Liu S</pubmed_authors><pubmed_authors>Huang LC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Construction of a single nucleotide variant score-related gene-based prognostic model in hepatocellular carcinoma: analysis of multi-independent databases and validation in vitro.</name><description>&lt;h4>Background&lt;/h4>The accumulation of single nucleotide variants (SNVs) and the emergence of neoantigens can affect tumour proliferation and the immune microenvironment. However, the SNV-related immune microenvironment characteristics and key genes involved in hepatocellular carcinoma (HCC) are still unclear. We aimed to evaluate differences in the SNV-related immune microenvironment, construct a prognostic model and validate the key genes in vitro.&lt;h4>Methods&lt;/h4>The categories of samples were defined by the expression of SNV score-related genes to evaluate the differences in mutational features, immune environment and prognosis. The survival model was constructed with survival-associated genes and verified in two independent test datasets. RCAN2, the key gene screened out for biofunctio</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Nov</publication><modification>2026-05-08T12:07:18.938Z</modification><creation>2022-02-11T13:03:45.208Z</creation></dates><accession>S-EPMC8600893</accession><cross_references><pubmed>34794449</pubmed><doi>10.1186/s12935-021-02321-z</doi></cross_references></HashMap>