Prevalence and Pattern of GATA3 Immunohistochemical Expression in Female Genital Tract Adenocarcinomas.

Adenocarcinoma Female genital tract GATA3 Immunohistochemistry

Journal

Iranian journal of pathology
ISSN: 1735-5303
Titre abrégé: Iran J Pathol
Pays: Iran
ID NLM: 101515128

Informations de publication

Date de publication:
2024
Historique:
received: 24 11 2022
accepted: 27 01 2024
medline: 9 8 2024
pubmed: 9 8 2024
entrez: 9 8 2024
Statut: ppublish

Résumé

GATA3 immunohistochemistry has been described as a highly sensitive marker in determining carcinomas of breast and urothelial origin. In the gynecologic system, it can be used as a marker to diagnose mesonephric or mesonephric-like carcinomas and trophoblastic tumors. The present study was performed to determine the diagnostic value of GATA3 in gynecological adenocarcinomas. A total of 187 samples from different types of endometrial, endocervical, and ovarian carcinomas were analyzed for intensity and percentage of GATA3 expression in tumor cells. The relationship between GATA3 expression and clinicopathological parameters was investigated. A total of 187 patients including 101 ovarian, 77 endometrial, and 9 endocervical adenocarcinomas were investigated. Weak and focal expression of this marker was observed in 5. 1% (4/77) endometrial, 12.9% (13/101) ovarian, and 11.1% (1/9) endocervical adenocarcinomas. The mean H score in all subtypes was less than 10.6 (2-35). There was no statistically significant correlation between GATA3 expression in tumor cells with clinical stage, and tumor recurrence or metastasis. GATA3 is infrequently, weak, or focally expressed in most of the common gynecological adenocarcinomas.

Sections du résumé

Background & Objective UNASSIGNED
GATA3 immunohistochemistry has been described as a highly sensitive marker in determining carcinomas of breast and urothelial origin. In the gynecologic system, it can be used as a marker to diagnose mesonephric or mesonephric-like carcinomas and trophoblastic tumors. The present study was performed to determine the diagnostic value of GATA3 in gynecological adenocarcinomas.
Methods UNASSIGNED
A total of 187 samples from different types of endometrial, endocervical, and ovarian carcinomas were analyzed for intensity and percentage of GATA3 expression in tumor cells. The relationship between GATA3 expression and clinicopathological parameters was investigated.
Results UNASSIGNED
A total of 187 patients including 101 ovarian, 77 endometrial, and 9 endocervical adenocarcinomas were investigated. Weak and focal expression of this marker was observed in 5. 1% (4/77) endometrial, 12.9% (13/101) ovarian, and 11.1% (1/9) endocervical adenocarcinomas. The mean H score in all subtypes was less than 10.6 (2-35). There was no statistically significant correlation between GATA3 expression in tumor cells with clinical stage, and tumor recurrence or metastasis.
Conclusion UNASSIGNED
GATA3 is infrequently, weak, or focally expressed in most of the common gynecological adenocarcinomas.

Identifiants

pubmed: 39118796
doi: 10.30699/IJP.2024.2016228.3217
pmc: PMC11304466
doi:

Types de publication

Journal Article

Langues

eng

Pagination

218-224

Informations de copyright

© 2024.

Déclaration de conflit d'intérêts

The authors declare a conflict of interest.

Auteurs

Elham Mirzaian (E)

Department of Pathology, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.

Tahereh Doustmohammadi (T)

Department of Pathology, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehan, Iran.

Mahshid Panahi (M)

Department of Pathology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Soheila Sarmadi (S)

Department of Pathology, Yas Women Hospital, Tehran University of Medical Sciences, Tehran, Ian.

Fereshteh Ameli (F)

Department of Pathology, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehan, Iran.

Fatemeh Nili (F)

Department of Pathology, Imam Khomeini Hospital Complex, Tehran University of Medical Sciences, Tehan, Iran.

Classifications MeSH