Evidence map›Paper›PMID 40476267›Full record

ArticleFrontiers in genetics2025

Whole exome sequencing and bioinformatics reveal PMAIP1 and PDGFRL as immune-related gene markers in follicular thyroid carcinoma.

Haobo Wang, Fangjian Shang, Xia Jiang, Zhongxin Li, Dongyun Li, Chuanmin Zhou, Bo Pang, Longfei Kang, Bo Liu, Zengren Zhao

Abstract read
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Article in Frontiers in genetics, 2025. 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

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Haobo Wang *Department of General Surgery, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Fangjian Shang *Department of General Surgery, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Xia JiangDepartment of General Surgery, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Zhongxin LiDepartment of General Surgery, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Dongyun LiDepartment of General Surgery, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Chuanmin ZhouDepartment of General Surgery, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Bo PangDepartment of General Surgery, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Longfei KangDepartment of General Surgery, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Bo LiuDepartment of General Surgery, The First Hospital of Hebei Medical University, Shijiazhuang, China.
Zengren ZhaoDepartment of General Surgery, The First Hospital of Hebei Medical University, Shijiazhuang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The primary clinical challenge associated with follicular thyroid carcinoma (FTC) lies in accurately diagnosing the condition, particularly in distinguishing it with follicular thyroid adenoma (FTA) due to their overlapping cytomorphological features and sonographic characteristics. Methods: Whole exome sequencing (WES) techniques and Gene Expression Omnibus (GEO) database were utilized to analyze genomic difference between FTC and FTA, with a specific focus on immune-related genes. The hub genes were subjected to enrichment analysis, immune infiltration analysis, protein-protein interaction (PPI) analysis, and receiver operating characteristic (ROC) curve analysis. Then utilized quantitative real-time polymerase chain reaction (qRT-PCR) and immunohistochemistry (IHC) to validate the expression levels of PMAIP1 and PDGFRL at the cellular and tissue levels. Results: The findings of WES and bioinformatics analysis indicated that PMAIP1 and PDGFRL were potential mutated immune-related genes in FTC, in comparison to FTA, the expression of PMAIP1 is up-regulated in FTC while PDGFRL is down-regulated, demonstrating promising diagnostic efficacy. Enrichment analysis and immune infiltration analysis suggested that PMAIP1 and PDGFRL may serve as potential therapeutic targets for FTC. The results of the validation at both cellular and tissue levels indicated an up-regulation of PMAIP1 and a down-regulation of PDGFRL in FTC, consistent with the results from bioinformatics analysis. Discussion: In conclusion, it is the first research to revealed PMAIP1 and PDGFRL as potential novel immunodiagnostic markers for FTC, shedding light on their potential biological significance in this context, and offering potential valuable clinical applications.

Indexed as

bioinformaticsfollicular thyroid adenomafollicular thyroid carcinomaPMAIP1; PDGFRLwhole exome sequencing

Identifiers

PMID40476267
PMCPMC12137315

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