Gene, Journal Year: 2024, Volume and Issue: 935, P. 149084 - 149084
Published: Nov. 8, 2024
Language: Английский
Gene, Journal Year: 2024, Volume and Issue: 935, P. 149084 - 149084
Published: Nov. 8, 2024
Language: Английский
Neuroscience and Behavioral Physiology, Journal Year: 2025, Volume and Issue: unknown
Published: Feb. 25, 2025
Language: Английский
Citations
0Journal of Pain, Journal Year: 2025, Volume and Issue: unknown, P. 105378 - 105378
Published: March 1, 2025
Language: Английский
Citations
0Cell Death and Disease, Journal Year: 2024, Volume and Issue: 15(11)
Published: Nov. 16, 2024
Abstract Breast cancer is one of the most prevalent and diverse malignancies, and, with global cases increasing, need for biomarkers to inform individual sensitivity chemotherapeutics has never been greater. Our retrospective clinical analysis predicted that expression fragile site-associated tumor suppressor (FATS) gene was associated breast neoadjuvant chemotherapy paclitaxel. In vitro experiments subsequently demonstrated FATS significantly increased inhibitory effects paclitaxel on cells’ migration, growth, survival. An interaction screen revealed interacted MYH9 promoted its degradation via ubiquitin-proteasome pathway, thereby downregulating Wnt signaling. By overexpressing MYH9, we enhanced paclitaxel-induced apoptosis in cells by degrading downregulate pathway. We also a mouse xenograft model chemosensitivity vivo. This study presents new mechanism which interacts suppress Wnt/β-catenin signaling pathway induce apoptosis, thus enhancing chemotherapy. The results propose novel predicting Finally, provide vivo evidence combination IWR-1, inhibitor, synergistically suppresses laying foundation future trials this drug combination. These therefore number potential solutions more precise treatment patients future.
Language: Английский
Citations
1Gene, Journal Year: 2024, Volume and Issue: 935, P. 149084 - 149084
Published: Nov. 8, 2024
Language: Английский
Citations
0