Expression of cytokeratin 7/20 and Ki67 in Helicobacter pylori-associated gastritis and intestinal metaplasia.


Journal

Journal of infection in developing countries
ISSN: 1972-2680
Titre abrégé: J Infect Dev Ctries
Pays: Italy
ID NLM: 101305410

Informations de publication

Date de publication:
29 Jul 2024
Historique:
received: 27 02 2023
accepted: 14 10 2023
medline: 30 7 2024
pubmed: 30 7 2024
entrez: 30 7 2024
Statut: epublish

Résumé

Cytokeratins (CKs) have been associated with precancerous and cancerous gastric lesions in patients with Helicobacter pylori-associated chronic gastritis, making them useful for diagnosing epithelial tumors. A retrospective study was conducted utilizing 200 formalin-fixed paraffin-embedded gastric biopsy samples collected from the lesser curvature of the stomach. Samples from the control group, patients with H. pylori infection, and patients with H. pylori-associated gastritis, with complete and incomplete intestinal metaplasia (IM) were immunostained. Monoclonal antibodies were utilized to determine the expression of CK7, CK20, and Ki-67. Patients infected with H. pylori had strong CK20 expression on the surface, and weak CK7 expression on the surface and deep glands; while non-specific chronic gastritis patients had weak focal CK7 expression and strong CK20 expression. The normal gastric mucosa of patients in the control group had relatively weak CK7 expression, restricted to a few cells in the neck and deep glands. CK20 showed diffuse strong reactivity on the surface. On the other hand, patients with complete IM showed a CK7 staining pattern that was either negative or weakly focal on the surface and crypts associated with diffuse surface CK20 and focal crypt staining corresponding to gastric type IM. The Ki67 proliferating index was low (≤ 15%) in H. pylori infected patients, high (> 30%) in patients with incomplete IM, and intermediate (16-30%) in patients with complete IM. These results indicate a significant link between the expressions of CK7/CK20 and Ki67 in patients afflicted with H. pylori and IM.

Identifiants

pubmed: 39078783
doi: 10.3855/jidc.18150
doi:

Substances chimiques

Ki-67 Antigen 0
Keratin-20 0
Keratin-7 0
MKI67 protein, human 0
KRT20 protein, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1032-1040

Informations de copyright

Copyright (c) 2024 Ava T Ismael, Rafal A Abdulhameed, Jalal A Jalal, Rawaz D Tawfeeq, Aram Ommar, Aveen Jalal.

Déclaration de conflit d'intérêts

No Conflict of Interest is declared

Auteurs

Ava T Ismael (AT)

Department of Pathology, College of Pharmacy, Hawler Medical University, Erbil, Iraq.

Rafal A Abdulhameed (RA)

Department of Basic Sciences/Pathology, College of Medicine, Hawler Medical University, Erbil, Iraq.

Jalal A Jalal (JA)

Department of Basic Sciences/Pathology, College of Medicine, Hawler Medical University, Erbil, Iraq.

Rawaz D Tawfeeq (RD)

Pathophysiology, Department of Clinical Analysis, College of Pharmacy, Hawler Medical University, Erbil, Iraq.

Aram Ommar (A)

Department of Clinical Pharmacy, College of Pharmacy, Hawler Medical University, Erbil, Iraq.

Aveen Jalal (A)

School of Pharmacy, Nottingham University, Nottingham, United Kingdom.

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