Evidence map›Paper›PMID 41891942›Full record

ArticleThe journal of pathology. Clinical research2026

ATM immunohistochemistry as an effective screening method for POLE variants among endometrial carcinomas lacking mismatch repair deficiency and p53 abnormalities.

Xinyi Huang, Yingmei Wang, Wenjing Ni, Luyang Zhong, Yang Qin, Shujun Zeng, Hong Xu, Yuling Qu, Peizhen Hu, Jing Zhang

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Article in The journal of pathology. Clinical research, 2026. 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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5 · Who and what money

Authors and funding

10 authors.

Xinyi Huang *Department of Pathology, Xijing Hospital, The Fourth Military Medical University, Xi'an, PR China.
Yingmei Wang *Department of Pathology, Xijing Hospital, The Fourth Military Medical University, Xi'an, PR China.
Wenjing Ni *Department of Pathology, Xijing Hospital, The Fourth Military Medical University, Xi'an, PR China.
Luyang ZhongDepartment of Psychology and Brain Science, College of Letters and Science, University of California, Santa Barbara, CA, USA.
Yang QinDepartment of Pathology, Xijing Hospital, The Fourth Military Medical University, Xi'an, PR China.
Shujun ZengDepartment of Pathology, Xijing Hospital, The Fourth Military Medical University, Xi'an, PR China.
Hong XuDepartment of Pathology, Xijing Hospital, The Fourth Military Medical University, Xi'an, PR China.
Yuling QuDepartment of Pathology, Xijing Hospital, The Fourth Military Medical University, Xi'an, PR China.
Peizhen HuDepartment of Pathology, Xijing Hospital, The Fourth Military Medical University, Xi'an, PR China.
Jing ZhangDepartment of Pathology, Xijing Hospital, The Fourth Military Medical University, Xi'an, PR China.ORCID https://orcid.org/0000-0001-7719-6943

Funding

Innovation Medical Research Translational Promotion Project of Xijing Hospital of the Fourth Military Medical University XJZT25CX02Key Research and Development Projects of Shaanxi Province 2024GX-YBXM-123National Natural Science Foundation of China 82072869
6 · The paper itself

Abstract

The molecular classification of endometrial carcinomas (ECs) is now integrated into clinical practice. However, identification of polymerase-ε (POLE) variants remains reliant on DNA sequencing, which limits broader implementation. Given the strong prognostic value of pathogenic POLE mutations and the established efficacy of immunohistochemistry (IHC) for detecting mismatch repair (MMR) deficiency and p53 abnormalities, there is a clear need for IHC-based screening strategies to identify patients likely to carry POLE variants and prioritize them for confirmatory sequencing. In this study, we analyzed 24 cases with POLE pathogenic mutations (POLEmut ECs), 3 with benign POLE variants, and 32 matched cases with no specific molecular profile (NSMP) from a cohort of 378 ECs. IHC evaluation of the ataxia telangiectasia mutated (ATM) protein revealed that POLE-mutated ECs (with pathogenic or benign POLE variants) exhibited significantly higher frequencies of non-diffuse positive staining patterns, including null, heterogeneous positive, and subclonal loss, compared with NSMP cases. Targeted next-generation sequencing of all exons across 474 cancer-related genes in the 27 POLE-mutated ECs and 20 NSMP cases with ATM non-diffuse positive staining patterns confirmed that POLE-mutated ECs typically had high tumor mutational burden and were enriched for ATM truncating variants. ATM molecular alterations, including various variant subtypes and multisite mutations, also closely correlated with these staining patterns. Based on these findings, we refined the ATM IHC interpretation framework to integrate staining patterns with sequencing data for improved molecular correlation. Specifically, the null and subclonal loss patterns showed high specificity (96.9%), positive predictive value (94.1%), and accuracy (79.7%) for identifying POLE variants. Notably, the null pattern appeared exclusively in ECs with pathogenic POLE mutations. These results suggest that ATM IHC staining is an effective screening tool for identifying patients who may benefit from confirmatory POLE sequencing among those lacking MMR deficiency or p53 abnormalities.

Indexed as

Ataxia Telangiectasia Mutated ProteinsBiomarkers, TumorDNA Mismatch RepairDNA Polymerase IIEndometrial NeoplasmsImmunohistochemistryPoly-ADP-Ribose Binding ProteinsTumor Suppressor Protein p53AgedDNA Mutational AnalysisFemaleHigh-Throughput Nucleotide SequencingHumansMiddle AgedMutationAtaxia Telangiectasia Mutated ProteinsATM protein, humanBiomarkers, TumorDNA Polymerase IIPOLE protein, humanPoly-ADP-Ribose Binding ProteinsTP53 protein, humanTumor Suppressor Protein p53ataxia telangiectasia mutated (ATM)endometrial carcinomaimmunohistochemistryno specific molecular profile (NSMP)polymerase‐ε (POLE)

Identifiers

PMID41891942
PMCPMC13093816

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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.