Immunohistological expression of oestrogen receptor, progesterone receptor, mammaglobin, human epidermal growth factor receptor 2 and GATA-binding protein 3 in non-small-cell lung cancer.


Journal

Histopathology
ISSN: 1365-2559
Titre abrégé: Histopathology
Pays: England
ID NLM: 7704136

Informations de publication

Date de publication:
Dec 2020
Historique:
received: 20 04 2020
revised: 27 06 2020
accepted: 02 07 2020
pubmed: 8 7 2020
medline: 24 8 2021
entrez: 8 7 2020
Statut: ppublish

Résumé

Non-small-cell lung cancer (NSCLC) and breast cancer are common entities. Staining for oestrogen receptor (ER), progesterone receptor (PgR), mammaglobin (MAMG) and GATA-binding protein 3 (GATA3) is frequently performed to confirm a mammary origin in the appropriate diagnostic setting. However, comprehensive data on the immunohistological expression of these markers in NSCLC are limited. Therefore, the aim of this study was to analyse a large cohort of NSCLCs and correlate the staining results with clinicopathological variables. A tissue microarray was stained for ER, PgR, MAMG, human epidermal growth factor receptor 2 (HER2), and GATA3, and included 636 adenocarcinomas (ADCs), 536 squamous cell carcinomas (SqCCs), 65 large-cell-carcinomas, 34 pleomorphic carcinomas, and 20 large-cell neuroendocrine carcinomas. HER2 status was determined for immunohistochemically positive cases with chromogenic in-situ hybridisation. Markers with a proportion of ≥5% positive cases in ADC and SqCC were considered for survival analysis. Among ADCs, 62 (10%), 17 (3%), one (<1%), seven (1%), and 49 (8%) cases were positive for ER, PgR, MAMG, HER2, and GATA3, respectively. Among SqCCs, 10 (2%), 14 (3%), two (<1%) and 109 (20%) cases were positive for ER, PgR, HER2, and GATA3, but none of the samples showed positivity for MAMG. ER positivity was associated with ADC, female sex, smaller tumour size, and lower clinical stage. None of the markers had an impact on survival. We report on ER, PgR, MAMG, HER2 and GATA3 expression in a large cohort of NSCLCs. Interpretation of these markers in the differential diagnostic setting should be based on a multimarker panel.

Identifiants

pubmed: 32634256
doi: 10.1111/his.14203
doi:

Substances chimiques

Biomarkers, Tumor 0
GATA3 Transcription Factor 0
GATA3 protein, human 0
Mammaglobin A 0
Receptors, Progesterone 0
ERBB2 protein, human EC 2.7.10.1
Receptor, ErbB-2 EC 2.7.10.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

900-914

Informations de copyright

© 2020 The Authors. Histopathology published by John Wiley & Sons Ltd.

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Auteurs

Katharina Kriegsmann (K)

Department of Internal Medicine V, Haematology, Oncology and Rheumatology, University Hospital Heidelberg, Heidelberg, Germany.

Christiane Zgorzelski (C)

Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.

Thomas Muley (T)

Translational Lung Research Centre Heidelberg, Member of the German Centre for Lung Research (DZL), Thoraxklinik at Heidelberg University, Heidelberg, Germany.
Translational Research Unit, Thoraxklinik at Heidelberg University, Heidelberg, Germany.

Petros Christopoulos (P)

Department of Thoracic Oncology, Thoraxklinik at Heidelberg University, Heidelberg, Germany.

Moritz von Winterfeld (M)

Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.

Esther Herpel (E)

Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.

Benjamin Goeppert (B)

Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.

Gunhild Mechtersheimer (G)

Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.

Peter Sinn (P)

Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.

Albrecht Stenzinger (A)

Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.
Translational Lung Research Centre Heidelberg, Member of the German Centre for Lung Research (DZL), Thoraxklinik at Heidelberg University, Heidelberg, Germany.

Peter Schirmacher (P)

Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.

Hauke Winter (H)

Translational Lung Research Centre Heidelberg, Member of the German Centre for Lung Research (DZL), Thoraxklinik at Heidelberg University, Heidelberg, Germany.
Translational Research Unit, Thoraxklinik at Heidelberg University, Heidelberg, Germany.
Department of Thoracic Surgery, Thoraxklinik at Heidelberg University, Heidelberg, Germany.

Monika Eichinger (M)

Department of Radiology, Thoraxklinik at Heidelberg University, Heidelberg, Germany.

Arne Warth (A)

Institute of Pathology, Cytopathology, and Molecular Pathology, UEGP MVZ Gießen/Wetzlar/Limburg, Limburg, Germany.

Mark Kriegsmann (M)

Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.
Translational Lung Research Centre Heidelberg, Member of the German Centre for Lung Research (DZL), Thoraxklinik at Heidelberg University, Heidelberg, Germany.
Translational Research Unit, Thoraxklinik at Heidelberg University, Heidelberg, Germany.

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