Evidence map›Paper›PMID 41462113›Full record

ArticleBMC gastroenterology2025

PAX5 expression and its diagnostic utility in gastroenteropancreatic neuroendocrine neoplasm.

Kun Wang, Xiaoying Liu, Jie Zhao, Zhihong Chen

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Article in BMC gastroenterology, 2025. 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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1 · What the graph read from it

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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

4 authors.

Kun WangDepartment of Pathology, Hunan Provincial People's Hospital and The first-affiliated hospital of Hunan normal university, Changsha, 410005, China.
Xiaoying LiuDepartment of Pathology, Hunan Provincial People's Hospital and The first-affiliated hospital of Hunan normal university, Changsha, 410005, China.
Jie ZhaoDepartment of Pathology, Hunan Provincial People's Hospital and The first-affiliated hospital of Hunan normal university, Changsha, 410005, China.
Zhihong ChenDepartment of Pathology, Hunan Provincial People's Hospital and The first-affiliated hospital of Hunan normal university, Changsha, 410005, China. zhchen1997@hunnu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) are common tumors of the digestive system. Although their histological diagnosis is usually straightforward, the differential diagnosis between neuroendocrine tumors G3 (NET G3) and neuroendocrine carcinomas (NECs) may be challenging at times due to a similar immunophenotype and morphology in a small number of cases. AIMS AND

methodsThe objective of this study was to assess the expression and diagnostic value of PAX5 in GEP-NENs. Immunohistochemical (IHC) analysis for PAX5 was carried out in a large cohort of GEP-NENs, including 39 GEP-NECs and 62 GEP-NETs.

resultsUsing a semi-quantitative scoring method, PAX5 was shown to be expressed in 30 of 39 GEP-NECs (77%), with 27 of 39 cases (69%) having positivity ≥ 10% in the cells. In particular, GEP-NECs with a high proliferative index had more PAX5-positive cells. None of the cases of GEP-NET G1 and G2 expressed PAX5, while only 2/12 cases of GEP-NET G3 (17%) were positive for PAX5, with PAX5 positivity observed in 1–10% and 10–50% of cells, respectively. The difference in PAX5 expression between GEP-NETs and GEP-NECs was statistically significant (3% vs. 77%, P < 0.001).

conclusionsPAX5 can be used as a complementary diagnostic IHC marker for GEP-NECs. In addition, PAX5 can be considered in cases when it is difficult to distinguish between GEP-NECs and GEP-NET G3.

Indexed as

Biomarkers, TumorCarcinoma, NeuroendocrineIntestinal NeoplasmsNeuroendocrine TumorsPancreatic NeoplasmsPAX5 Transcription FactorStomach NeoplasmsAdultAgedDiagnosis, DifferentialFemaleHumansImmunohistochemistryMaleMiddle AgedBiomarkers, TumorPAX5 protein, humanPAX5 Transcription FactorGastroenteropancreaticImmunohistochemistryNeuroendocrine neoplasmPathologic diagnosisPAX5

Identifiers

PMID41462113
PMCPMC12751932

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