Evidence map›Paper›PMID 41885285›Full record

ArticleCancer biomarkers : section A of Disease markers

Integrative bioinformatics analysis identifies HCCS as a prognostic and therapeutic biomarker in lung cancer.

Sm Faysal Bellah, Md Alim Hossen, S M Saker Billah

Abstract read
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Article in Cancer biomarkers : section A of Disease markers. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Sm Faysal BellahDepartment of Pharmacy, Pabna University of Science and Technology, Pabna, Bangladesh.ORCID 0000-0002-8626-8547
Md Alim HossenDepartment of Physical Sciences, Independent University, Bangladesh, Dhaka, Bangladesh.ORCID 0000-0002-3598-0729
S M Saker BillahDepartment of Chemistry, National University, Gazipur, Bangladesh.ORCID 0000-0002-4945-9002

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BackgroundLung cancer remains one of the leading causes of cancer-related mortality worldwide. Holocytochrome c synthase (HCCS), a mitochondrial enzyme involved in apoptosis and energy metabolism, has been implicated in tumorigenesis; however, its role in lung cancer is not well defined.AimThis study aimed to elucidate the prognostic and therapeutic potential of HCCS in lung cancer through integrative bioinformatics analyses.MethodsTranscriptomic, methylation, and clinical data from TCGA were analyzed using TNMplot, UALCAN, and TIMER2.0 to evaluate HCCS expression, promoter methylation, immune infiltration, and prognostic relevance in lung adenocarcinoma (LUAD) and lung squamous cell carcinoma (LUSC). Meta-analysis of 18 independent cohorts from LUNG CANCER EXPLORER and four GEO datasets validated expression patterns, while Kaplan-Meier analysis assessed survival outcomes.ResultsHCCS was significantly upregulated in LUAD and LUSC and showed promoter hypermethylation in LUAD. Meta-analysis and external validation confirmed its overexpression. Patients with low HCCS expression exhibited poorer overall survival, suggesting a potential tumor-suppressive effect. HCCS expression positively correlated with immune cell infiltration and co-expressed genes enriched in mitochondrial and apoptotic pathways.ConclusionHCCS may serve as a prognostic and therapeutic biomarker in lung cancer, linking mitochondrial regulation, epigenetic modification, and immune interactions.

Indexed as

Biomarkers, TumorComputational BiologyLung NeoplasmsDNA MethylationGene Expression ProfilingGene Expression Regulation, NeoplasticHumansPrognosisPromoter Regions, GeneticBiomarkers, TumorbiomarkerHCCSimmune infiltrationlung adenocarcinomameta-analysismethylation

Identifiers

PMID41885285
PMCPMC13068008

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