Evidence map›Paper›PMID 41912255›Full record

ArticleAPMIS : acta pathologica, microbiologica, et immunologica Scandinavica2026

Correlation of TP53 Mutations With p53 Expression and Ki-67 Index in Pulmonary Large Cell Neuroendocrine Carcinomas.

Martin Stampe, Jonas Smidt, Linea Melchior, Morten Grauslund, Birgitte Federspiel, Eric Santoni-Rugiu, Thomas Hartvig Lindkær Jensen

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Article in APMIS : acta pathologica, microbiologica, et immunologica Scandinavica, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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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

7 authors.

Martin StampeDepartment of Pathology, Rigshospitalet, Copenhagen, Denmark.ORCID https://orcid.org/0009-0001-2803-9463
Jonas SmidtDepartment of Pathology, Rigshospitalet, Copenhagen, Denmark.
Linea MelchiorDepartment of Pathology, Rigshospitalet, Copenhagen, Denmark.ORCID https://orcid.org/0000-0001-7061-8859
Morten GrauslundDepartment of Pathology, Rigshospitalet, Copenhagen, Denmark.
Birgitte FederspielDepartment of Pathology, Rigshospitalet, Copenhagen, Denmark.
Eric Santoni-RugiuDepartment of Pathology, Rigshospitalet, Copenhagen, Denmark.
Thomas Hartvig Lindkær JensenDepartment of Pathology, Rigshospitalet, Copenhagen, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study explores the locations and distribution of mutations in the exons of the TP53 gene in pulmonary large cell neuroendocrine carcinomas (LCNEC) and the corresponding expression of p53 as well as the Ki-67 proliferation index. Real-world data from routine diagnostics were collected retrospectively from 149 consecutive cases of pulmonary LCNEC. They included next-generation sequencing (NGS) of the TP53 gene along with evaluation of p53 and Ki-67 expression with immunohistochemistry (IHC). Abnormal p53 expression was defined as strong positive nuclear reaction in more than 20% of the tumor cells or complete absence of immunostaining in tumor cells. Both p53 expression and Ki-67 proliferation index correlated with TP53 mutations. In addition, a statistically significant increase in Ki-67 expression was found for cases with abnormal staining of p53 compared to samples with normal staining. We found that IHC staining for p53 can identify TP53 mutations in pulmonary LCNEC with an overall concordance of 76.6%. Moreover, both pathological patterns of p53 immunostaining and NGS-detected TP53 mutations were associated with higher Ki-67 proliferation indices.

Indexed as

Carcinoma, Large CellCarcinoma, NeuroendocrineKi-67 AntigenLung NeoplasmsMutationTumor Suppressor Protein p53AdultAgedFemaleHigh-Throughput Nucleotide SequencingHumansImmunohistochemistryMaleMiddle AgedRetrospective StudiesKi-67 AntigenTP53 protein, humanTumor Suppressor Protein p53immunohistochemistryKi‐67pulmonary large cell neuroendocrine carcinomasthoracic pathologyTP53 mutations and p53 expression

Identifiers

PMID41912255
PMCPMC13035449

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