<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10</volume><submitter>Huang S</submitter><pubmed_abstract>&lt;b>Background:&lt;/b> Actin-related protein 2/3 complex subunit 2 (ARPC2) plays a fundamental role in actin filament nucleation and is critical for tumor cell migration and invasion. However, its abnormal expression, clinical significance, and biological function in human pan-cancer have been poorly explored. Thus, we focused on ARPC2 as an entry point for identifying novel pan-cancer prognostic biomarkers. &lt;b>Methods:&lt;/b> The Cancer Genome Atlas (TCGA) and the Genotype-Tissue Expression (GTEx) databases were used to assess the differential expression of ARPC2 in pan-cancer. The Human Protein Atlas was used for the tissue/cell-specific expression analysis of ARPC2. The genetic alteration information of ARPC2 was obtained from the cBioPortal database and the GSCALite platform. The prognostic v</pubmed_abstract><journal>Frontiers in cell and developmental biology</journal><pagination>896080</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9207441</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>ARPC2: A Pan-Cancer Prognostic and Immunological Biomarker That Promotes Hepatocellular Carcinoma Cell Proliferation and Invasion.</pubmed_title><pmcid>PMC9207441</pmcid><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Huang S</pubmed_authors><pubmed_authors>Li D</pubmed_authors><pubmed_authors>Dong C</pubmed_authors><pubmed_authors>Xu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>ARPC2: A Pan-Cancer Prognostic and Immunological Biomarker That Promotes Hepatocellular Carcinoma Cell Proliferation and Invasion.</name><description>&lt;b>Background:&lt;/b> Actin-related protein 2/3 complex subunit 2 (ARPC2) plays a fundamental role in actin filament nucleation and is critical for tumor cell migration and invasion. However, its abnormal expression, clinical significance, and biological function in human pan-cancer have been poorly explored. Thus, we focused on ARPC2 as an entry point for identifying novel pan-cancer prognostic biomarkers. &lt;b>Methods:&lt;/b> The Cancer Genome Atlas (TCGA) and the Genotype-Tissue Expression (GTEx) databases were used to assess the differential expression of ARPC2 in pan-cancer. The Human Protein Atlas was used for the tissue/cell-specific expression analysis of ARPC2. The genetic alteration information of ARPC2 was obtained from the cBioPortal database and the GSCALite platform. The prognostic v</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-05T13:28:59.546Z</modification><creation>2024-11-05T20:36:45.869Z</creation></dates><accession>S-EPMC9207441</accession><cross_references><pubmed>35733852</pubmed><doi>10.3389/fcell.2022.896080</doi></cross_references></HashMap>