The Role of Mesothelin in Gynecological Tumors and Its Significance in Targeted Therapies—A Review

Read full text
Authors: Weronika Kawecka, Jacek R. Wilczyński, Magdalena Tyczyńska, Michał Bielak, Bogdan Obrzut, Andrzej Semczuk
Cited by: 1
References: 142

Abstract

Mesothelin (MSLN) is a cell surface glycoprotein with limited expression in normal tissues but frequent overexpression in solid tumors, including gynecological malignancies. This review summarizes the state of the art on the biological role, diagnostic value, prognostic significance, and therapeutic potential of MSLN in ovarian, endometrial, and cervical cancers. Evidence from clinical and experimental studies indicates that MSLN contributes to tumor progression through interactions with CA125, promotion of cell adhesion and peritoneal metastasis, activation of oncogenic signaling pathways, modulation of immune responses, and development of chemoresistance. Elevated MSLN expression has been associated with advanced clinical stage of the disease, platinum resistance, and poorer survival outcomes, particularly in ovarian cancer patients, although prognostic findings remain inconsistent. Circulating soluble MSLN may serve as a minimally invasive biomarker and may improve diagnostic accuracy when combined with established markers. Therapeutic MSLN strategies-antibody-drug conjugates, CAR-T and NK cell therapies, monoclonal antibodies, immunotoxins, vaccines, and checkpoint blockade-provide promising pre-clinical and early clinical results, particularly in resistant or recurrent forms of the disease. Overall, MSLN constitutes a promising target for precision oncology in gynecological cancers, although further clinical studies are required to validate its diagnostic utility and optimize targeted therapeutic approaches.

Fields of Study & Subjects

Occupational and environmental lung diseases Infectious Disease Case Reports and Treatments Pleural and Pulmonary Diseases

Publication details

Journal / source
Cancers
Publisher
MDPI AG
Volume
18
Issue
11
Pages
1692–1692
Publication date
22 May 2026
Language
EN