
European Journal of Pharmacology, Год журнала: 2025, Номер unknown, С. 177712 - 177712
Опубликована: Май 1, 2025
Язык: Английский
European Journal of Pharmacology, Год журнала: 2025, Номер unknown, С. 177712 - 177712
Опубликована: Май 1, 2025
Язык: Английский
Cell Communication and Signaling, Год журнала: 2025, Номер 23(1)
Опубликована: Янв. 21, 2025
FGF21 regulates local and systemic metabolic homeostasis. High serum was found in obesity, syndrome, type 2 diabetes mellitus, coronary heart disease. The pathways linking obesity breast cancer remain elusive. We aimed to analyze the patients at diagnosis. Circulating levels 45 women (median age 59, range 32–88 years) 51 age-matched healthy controls were evaluated using a quantitative ELISA assay. Patients' samples obtained before surgery ahead of any previous therapy. Breast showed significantly elevated 267.13, 28.41-780.45) respect (76.86, 0.00-425.60) (p < 0.0001). A ROC curve determined cut-off value 130.64 pg/ml define positive or high levels. Based on this point, 30/45 (66.7%) as compared 18/51 (35.3%) controls. could be useful highly sensitive diagnosis biomarker for early detection. did not find significant association between levels, many clinical-pathological parameters primary Interestingly, statistically correlation body mass index (BMI). Furthermore, with had worst overall survival (Log Rank Test [Mantle Cox] p = 0.017). propose promising diagnostic prognosis oncological
Язык: Английский
Процитировано
1Cancers, Год журнала: 2025, Номер 17(2), С. 165 - 165
Опубликована: Янв. 7, 2025
Background/Objectives: Endocrine therapies that comprise anti-estrogens and aromatase inhibitors (AIs) are the standard treatment for estrogen receptor-positive (ER+) (Luminal A) breast cancer-the most prevalent subtype. However, emergence of resistance restricts their success by causing tumor relapse re-growth, which demands a switch towards other therapeutic approaches in order to minimize or overcome resistance. Indeed, this clinical limitation highlights search new molecules improve cancer treatment. Recently, strategies address multiple targets have been emerging, multi-target drugs potential become future anti-cancer molecules. Our group has searching compounds, as part this, our study aims understand three steroidal (AIs): 7α-methylandrost-4-en-17-one (6), 7α-methylandrost-4-ene-3,17-dione (10a) androsta-4,9(11)-diene-3,17-dione (13). Methods: Their vitro actions molecular mechanisms were elucidated sensitive ER+ aromatase-overexpressing cell line, MCF-7aro cells, well an AI-resistant LTEDaro cells. Results: All AIs (10 µM) prevented proliferation cells arresting cycle progression. Interestingly, all act androgen receptor (AR) agonists modulate ER levels, synthesis signaling induce apoptosis Additionally, these also re-sensitize resistant promoting apoptosis, offering benefit. Conclusions: Overall, polypharmacological compounds discovered that, acting AIs, modulators AR agonists, impair growth. is breakthrough on drug discovery it presents with appealing properties action cancer.
Язык: Английский
Процитировано
0European Journal of Pharmacology, Год журнала: 2025, Номер unknown, С. 177712 - 177712
Опубликована: Май 1, 2025
Язык: Английский
Процитировано
0