<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(5)</volume><submitter>Chen X</submitter><pubmed_abstract>Serum deprivation-response protein (SDPR), a phosphatidylserine-binding protein, which is known to have a promising role in caveolar biogenesis and morphology. However, its function in hepatocellular carcinoma (HCC) was still largely unknown. In this study, we discussed the characterization and identification of SDPR, and to present it as a novel apoptosis candidate in the incidence of HCC. We identified 81 HCC cases with lower SDPR expression in the tumor tissues with the help of qRT-PCR assay, and lower SDPR expression was potentially associated with poor prognostication. The phenotypic assays revealed that cell proliferation, invasion, and migration were profoundly connected with SDPR, both in vivo and in vitro. The data obtained from the gene set enrichment analysis (GSEA) carried out </pubmed_abstract><journal>Cell death &amp; disease</journal><pagination>425</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8087765</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Serum deprivation-response protein induces apoptosis in hepatocellular carcinoma through ASK1-JNK/p38 MAPK pathways.</pubmed_title><pmcid>PMC8087765</pmcid><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Guo Y</pubmed_authors><pubmed_authors>Wang G</pubmed_authors><pubmed_authors>Zhang Q</pubmed_authors><pubmed_authors>Wang K</pubmed_authors><pubmed_authors>Ma W</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Yao Y</pubmed_authors><pubmed_authors>Jiang X</pubmed_authors><pubmed_authors>Mei C</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Chen X</pubmed_authors><pubmed_authors>Wu X</pubmed_authors><pubmed_authors>Yuan Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Serum deprivation-response protein induces apoptosis in hepatocellular carcinoma through ASK1-JNK/p38 MAPK pathways.</name><description>Serum deprivation-response protein (SDPR), a phosphatidylserine-binding protein, which is known to have a promising role in caveolar biogenesis and morphology. However, its function in hepatocellular carcinoma (HCC) was still largely unknown. In this study, we discussed the characterization and identification of SDPR, and to present it as a novel apoptosis candidate in the incidence of HCC. We identified 81 HCC cases with lower SDPR expression in the tumor tissues with the help of qRT-PCR assay, and lower SDPR expression was potentially associated with poor prognostication. The phenotypic assays revealed that cell proliferation, invasion, and migration were profoundly connected with SDPR, both in vivo and in vitro. The data obtained from the gene set enrichment analysis (GSEA) carried out </description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2025-04-21T18:20:56.196Z</modification><creation>2025-04-05T17:13:28.528Z</creation></dates><accession>S-EPMC8087765</accession><cross_references><pubmed>33931585</pubmed><doi>10.1038/s41419-021-03711-x</doi></cross_references></HashMap>