ARID1a Gene as a Potential Early Marker to Tackle Endometriosis-Associated Ovarian Cancer.


Journal

Aging and disease
ISSN: 2152-5250
Titre abrégé: Aging Dis
Pays: United States
ID NLM: 101540533

Informations de publication

Date de publication:
17 Nov 2023
Historique:
received: 20 09 2023
accepted: 09 11 2023
medline: 29 11 2023
pubmed: 29 11 2023
entrez: 29 11 2023
Statut: aheadofprint

Résumé

The worries of women with endometriosis - a chronic gynecological disease affecting approximately 10% of women of childbearing age - about the increased risk of ovarian cancer are present worldwide. Endometriosis is a common, often painful, but benign gynecological disease that affects women. However, the pathogenesis remains elusive but is certainly multifactorial. Interestingly, endometriosis shares similarities with cancer. Therefore, women suffering from endometriosis fear an increased risk of ovarian cancer. In addition, these patients suffer from anxiety and depression. Previous studies have provided evidence that epithelial mutations in endometriosis or in the endometrium include certain inactivating mutations responsible for ovarian cancer, such as in the ARID1A gene.

Identifiants

pubmed: 38029403
pii: AD.2023.1109
doi: 10.14336/AD.2023.1109
doi:

Types de publication

Journal Article

Langues

eng

Auteurs

Pawel Kordowitzki (P)

Department of Preclinical and Basic Sciences, Nicolaus Copernicus University, Torun, Poland.
Department of Gynecology including Center of Oncological Surgery (CVK) and Department of Gynecology (CBF), European Competence Center for Ovarian Cancer, Charite, Berlin, Germany.

Sylvia Mechsner (S)

Department of Gynecology including Center of Oncological Surgery (CVK) and Department of Gynecology (CBF), European Competence Center for Ovarian Cancer, Charite, Berlin, Germany.

Jalid Sehouli (J)

Department of Gynecology including Center of Oncological Surgery (CVK) and Department of Gynecology (CBF), European Competence Center for Ovarian Cancer, Charite, Berlin, Germany.

Classifications MeSH