Wnt-7a is upregulated by norethisterone in human endometrial epithelial cells: a possible mechanism by which progestogens reduce the risk of estrogen-induced endometrial neoplasia

التفاصيل البيبلوغرافية
العنوان: Wnt-7a is upregulated by norethisterone in human endometrial epithelial cells: a possible mechanism by which progestogens reduce the risk of estrogen-induced endometrial neoplasia
المؤلفون: D Wallwiener, Roy Bicknell, Margaret Rees, Martin K. Oehler, Ian Z. MacKenzie
المصدر: Cancer letters. 186(1)
سنة النشر: 2002
مصطلحات موضوعية: Cancer Research, medicine.medical_specialty, Norethisterone, medicine.drug_class, medicine.medical_treatment, Biology, Endometrium, Internal medicine, Proto-Oncogene Proteins, medicine, Humans, RNA, Messenger, reproductive and urinary physiology, Cells, Cultured, Oligonucleotide Array Sequence Analysis, Progestogen, Estradiol, Endometrial cancer, Wnt signaling pathway, Hormone replacement therapy (menopause), Epithelial Cells, medicine.disease, Norethisterone acetate, female genital diseases and pregnancy complications, Endometrial Neoplasms, Up-Regulation, Wnt Proteins, Norethindrone Acetate, medicine.anatomical_structure, Endocrinology, Oncology, Gene Expression Regulation, Estrogen, Female, Norethindrone, hormones, hormone substitutes, and hormone antagonists, medicine.drug
الوصف: Progestogens are added to oestrogen in hormone replacement therapy regimens to reduce the risk of endometrial cancer. We have performed in vitro studies analysing gene expression of isolated normal endometrial epithelia cells (NEE) treated with estradiol and the progestogen norethisterone acetate (NETA). We report here for the first time upregulation of the Wnt-7a gene by NETA in estrogen treated NEE. Wnt genes are a large family of developmental genes associated with cellular responses such as oncogenesis. We therefore suggest that upregulation of Wnt-7a may be associated with the antineoplastic effects of progestogens on the endometrium.
تدمد: 0304-3835
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96f92129fb2bc96dd7cacd1d25afee68
https://pubmed.ncbi.nlm.nih.gov/12183078
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....96f92129fb2bc96dd7cacd1d25afee68
قاعدة البيانات: OpenAIRE