BPG is committed to discovery and dissemination of knowledge
Articles Published Processes
12/11/2025 8:20:57 AM | Browse: 93 | Download: 342
 |
Received |
|
2025-06-16 10:01 |
 |
Peer-Review Started |
|
2025-06-16 10:01 |
 |
First Decision by Editorial Office Director |
|
2025-07-03 11:09 |
 |
Return for Revision |
|
2025-07-04 01:43 |
 |
Revised |
|
2025-07-08 08:35 |
 |
Publication Fee Transferred |
|
|
 |
Second Decision by Editor |
|
2025-10-17 02:37 |
 |
Second Decision by Editor-in-Chief |
|
|
 |
Final Decision by Editorial Office Director |
|
2025-10-17 07:07 |
 |
Articles in Press |
|
2025-10-17 07:07 |
 |
Edit the Manuscript by Language Editor |
|
|
 |
Typeset the Manuscript |
|
2025-12-01 05:50 |
 |
Publish the Manuscript Online |
|
2025-12-11 08:20 |
| ISSN |
1948-5204 (online) |
| Open Access |
This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/ |
| Copyright |
© The Author(s) 2025. Published by Baishideng Publishing Group Inc. All rights reserved. |
| Article Reprints |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/247
|
| Permissions |
For details, please visit: http://www.wjgnet.com/bpg/gerinfo/207
|
| Publisher |
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA |
| Website |
http://www.wjgnet.com |
| Category |
Gastroenterology & Hepatology |
| Manuscript Type |
Basic Study |
| Article Title |
Transient receptor potential melastatin 6 and transient receptor potential melastatin 6/7 antagonists suppress colon adenocarcinoma HT-29 cells
|
| Manuscript Source |
Invited Manuscript |
| All Author List |
Nattida Kampuang, Siriporn Chamniansawat, Pawin Pongkorpsakol, Supisara Treveeravoot and Narongrit Thongon |
| ORCID |
|
| Funding Agency and Grant Number |
| Funding Agency |
Grant Number |
| National Science Research and Innovation Fund |
53/2567 |
|
| Corresponding Author |
Narongrit Thongon, Associate Professor, PhD, Department of Medical Sciences, Faculty of Allied Health Sciences, Burapha University, 169 Long-Hard Bangsaen Road, Saensook, Muang 20131, Chonburi, Thailand. narongritt@buu.ac.th |
| Key Words |
Cancer stem cells; Cellular Mg2+ content; Colorectal cancer; Transient receptor potential melastatin 6/7; Transient receptor potential melastatin 6 |
| Core Tip |
This study demonstrated that colorectal cancer (CRC) spheroids (SPs) exhibited significantly increased membrane expression and phosphorylation of transient receptor potential melastatin (TRPM) 6 and TRPM6/7 channels, which enhanced magnesium (Mg2+) influx and promoted intracellular Mg2+ accumulation. However, selective TRPM6 and TRPM6/7 inhibitors markedly suppressed Mg2+ influx, SP formation, cell viability, and migration and impaired cancer stem-like properties. These findings highlight the critical role of TRPM6/TRPM7-mediated Mg2+ transport in CRC progression and emphasize the potential of these channels as therapeutic targets for CRC SP elimination. |
| Publish Date |
2025-12-11 08:20 |
| Citation |
Kampuang N, Chamniansawat S, Pongkorpsakol P, Treveeravoot S, Thongon N. Transient receptor potential melastatin 6 and transient receptor potential melastatin 6/7 antagonists suppress colon adenocarcinoma HT-29 cells. World J Gastrointest Oncol 2025; 17(12): 110736 |
| URL |
https://www.wjgnet.com/1948-5204/full/v17/i12/110736.htm |
| DOI |
https://dx.doi.org/10.4251/wjgo.v17.i12.110736 |
All content on this site: Copyright © 1993-2026 Baishideng Publishing Group Inc, its licensors, and contributors. All rights are reserved, including those for text and data mining, AI training, and similar technologies. For all open access content, the relevant licensing terms apply.