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5/20/2024 8:23:18 AM | Browse: 94 | Download: 0
Publication Name World Journal of Clinical Oncology
Manuscript ID 91707
Country China
Category Cell Biology
Manuscript Type Editorial
Article Title New targets for cancer promotion and therapy in gliomas: Scinderin
Manuscript Source Invited Manuscript
All Author List Xi Wang and Lian-Xiang Luo
Funding Agency and Grant Number
Corresponding Author Lian-Xiang Luo, PhD, Adjunct Associate Professor, The Marine Biomedical Research Institute, Guangdong Medical University, No. 2 Wenming East Road, Zhanjiang 524000, Guangdong Province, China. luolianxiang321@gdmu.edu.cn
Key Words Glioma; Scinderin; Actin cytoskeleton; RhoA/FAK signaling; 1p/19q co-deletion
Core Tip The role of scinderin (SCIN) in cancer progression has been studied, but its role in glioma remains unknown. Lin et al found that the expression level of SCIN mRNA was positively correlated with the tumor grade of glioma. SCIN affected cytoskeletal remodeling and inhibited lamellipodia formation through RhoA/FAK signaling pathway, thereby facilitating the migration and invasion of glioma cells.
Citation <p>Wang X, Luo LX. New targets for cancer promotion and therapy in gliomas: Scinderin. <i>World J Clin Oncol</i> 2024; 15(6): 687-690</p>
Received
2024-01-03 01:26
Peer-Review Started
2024-01-03 01:26
To Make the First Decision
Return for Revision
2024-04-10 05:57
Revised
2024-04-27 16:23
Second Decision
2024-05-20 02:49
Accepted by Journal Editor-in-Chief
Accepted by Executive Editor-in-Chief
2024-05-20 08:23
Articles in Press
2024-05-20 08:23
Publication Fee Transferred
Edit the Manuscript by Language Editor
Typeset the Manuscript
2024-05-29 08:25
ISSN 2218-4333 (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/
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