Evidence map›Paper›PMID 41817384›Full record

ArticleCancer control : journal of the Moffitt Cancer Center

Overexpression of S100 Calcium-Binding Protein A2 is Associated With Poor Prognosis in Hepatocellular Carcinoma.

Xiaopeng Chen, Shaoqing Ma, Wenlong Zeng, Chuiguo Huang, Jianyang Guo

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Article in Cancer control : journal of the Moffitt Cancer Center. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Xiaopeng ChenDepartment of Hepatobiliary Surgery, The Second Hospital of Longyan, Longyan, Fujian, PR China.ORCID 0009-0002-0697-3631
Shaoqing MaDepartment of Hepatobiliary Surgery, The Second Hospital of Longyan, Longyan, Fujian, PR China.ORCID 0009-0000-0548-7127
Wenlong ZengDepartment of Hepatobiliary Surgery, The Second Hospital of Longyan, Longyan, Fujian, PR China.ORCID 0000-0002-3338-8799
Chuiguo HuangDepartment of Medicine and Therapeutics, Prince of Wales Hospital, The Chinese University of Hong Kong, Hong Kong, PR China.
Jianyang GuoDepartment of Hepatobiliary Surgery, The Second Hospital of Longyan, Longyan, Fujian, PR China.ORCID 0009-0009-7229-5315

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IntroductionS100 calcium-binding protein A2 (S100A2) is associated with various tumors. However, its expression profile, clinical relevance, and prognostic value in hepatocellular carcinoma (HCC) remain unclear; therefore, this study assessed S100A2 expression levels in HCC and adjacent normal tissues.MethodsTo investigate the role of S100A2 in HCC, RNA sequencing and DNA methylation data were obtained from The Cancer Genome Atlas (TCGA)-Liver Hepatocellular Carcinoma (LIHC) cohort comprising 374 tumor and 50 normal liver tissues. A retrospective cohort of 216 HCC patients was also evaluated for correlations between S100A2 expression and clinicopathological characteristics. In a subset of 62 paired tumor and adjacent normal tissues, S100A2 protein and mRNA levels were assessed by immunohistochemistry (IHC) and quantitative RT-PCR. Finally, the relationship between S100A2 overexpression and clinicopathological variables was examined using the Cox proportional hazards regression model.ResultsAnalysis of the TCGA-LIHC dataset revealed a marked elevation in S100A2 expression in tumor tissues compared to normal liver tissues. Consistently, DNA methylation analysis showed hypomethylation of several S100A2-associated CpG sites in liver hepatocellular carcinoma, suggesting a potential epigenetic mechanism for its upregulation. Correlation analysis demonstrated that increased S100A2 expression was associated with advanced histological grade, lymph node metastasis, serum alpha-fetoprotein level, microvascular invasion, tyrosine kinase inhibitor level, concurrent treatment, and higher Tumor, Node, Metastasis stage. Univariate analysis showed that elevated S100A2 levels were associated with significantly poorer recurrence-free survival (RFS) and overall survival (OS). Moreover, multivariate analysis identified S100A2 as an independent prognostic indicator for both RFS and OS. Kaplan-Meier survival curves also confirmed that patients with high S100A2 protein levels had significantly worse 5-year OS and RFS rates.ConclusionThese findings indicate that S100A2 overexpression is associated with poor prognosis in patients with HCC, highlighting its potential utility as a diagnostic biomarker.

Indexed as

Carcinoma, HepatocellularChemotactic FactorsLiver NeoplasmsS100 ProteinsBiomarkers, TumorDNA MethylationFemaleGene Expression Regulation, NeoplasticHumansMaleMiddle AgedPrognosisRetrospective StudiesBiomarkers, TumorChemotactic FactorsS100A2 protein, humanS100 Proteinshepatocellular carcinomaoverall survivalprognosisrecurrence-free survivalS100 calcium-binding protein A2

Identifiers

PMID41817384
PMCPMC12982858

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.