دورية أكاديمية

Role of the transient receptor potential melastatin 4 in inhibition effect of arsenic trioxide on the tumor biological features of colorectal cancer cell

التفاصيل البيبلوغرافية
العنوان: Role of the transient receptor potential melastatin 4 in inhibition effect of arsenic trioxide on the tumor biological features of colorectal cancer cell
المؤلفون: Zhan Gao, Jing Lv, Ting-Ting Tong, Kai Zhang, Yu-Xuan Han, Yu Zhao, Mei-Mei Shen, Yang Liu, Tao Ban, Yu Sun
المصدر: PeerJ, Vol 12, p e17559 (2024)
بيانات النشر: PeerJ Inc., 2024.
سنة النشر: 2024
المجموعة: LCC:Medicine
LCC:Biology (General)
مصطلحات موضوعية: TRPM4 channel, Arsenic trioxide, HCT116 cells, Colorectal cancer, Medicine, Biology (General), QH301-705.5
الوصف: Background To investigate the effects of arsenic trioxide (ATO) on human colorectal cancer cells (HCT116) growth and the role of transient receptor potential melastatin 4 (TRPM4) channel in this process. Methods The viability of HCT116 cells was assessed using the CCK-8 assay. Western blot analysis was employed to examine the protein expression of TRPM4. The apoptosis of HCT116 cells was determined using TUNEL and Flow cytometry. Cell migration was assessed through the cell scratch recovery assay and Transwell cell migration assay. Additionally, Transwell cell invasion assay was performed to determine the invasion ability of HCT116 cells. Results ATO suppressed the viability of HCT116 cells in a dose-dependent manner, accompanied by a decline in cell migration and invasion, and an increase in apoptosis. 9-phenanthroline (9-Ph), a specific inhibitor of TRPM4, abrogated the ATO-induced upregulation of TRPM4 expression. Additionally, blocking TRPM4 reversed the effects of ATO on HCT116 cells proliferation, including restoration of cell viability, migration and invasion, as well as the inhibition of apoptosis. Conclusion ATO inhibits CRC cell growth by inducing TRPM4 expression, our findings indicate that ATO is a promising therapeutic strategy and TRPM4 may be a novel target for the treatment of CRC.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2167-8359
Relation: https://peerj.com/articles/17559.pdf; https://peerj.com/articles/17559/; https://doaj.org/toc/2167-8359
DOI: 10.7717/peerj.17559
URL الوصول: https://doaj.org/article/85466df57f11457dbb05692efee327c3
رقم الأكسشن: edsdoj.85466df57f11457dbb05692efee327c3
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:21678359
DOI:10.7717/peerj.17559