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Publication Name World Journal of Stem Cells
Manuscript ID 126709
DOI 10.4252/wjsc.126709
Country China
Category Gastroenterology & Hepatology
Manuscript Type Review
Article Title Proliferative spasmolytic polypeptide-expressing metaplasia in gastric carcinogenesis: Stem cell origins, lineage plasticity, and clinical implications
Manuscript Source Unsolicited Manuscript
All Author List Wei-Jian Zhang, Yan-Zi Huang, Qiang Chen, Shu-Tong Zheng, Hui-Shan Yuan, Xin-Bo Chen, Yi-Zhong Liang, Xin-Xin Hong, Yi-Fei Xu, Hai-Wen Li, Yong Gao and Shao-Ju Guo
Funding Agency and Grant Number
Funding Agency Grant Number
National Natural Science Foundation of China 82608567, 82374348, and 82305133
Guangdong Medical Research Foundation B2026159
Shenzhen Science and Technology Program JCYJ20230807094659030
Sanming Project of Medicine in Shenzhen SZZYSM202211002
Shenzhen High-level Hospital Construction Fund
Corresponding Author Shao-Ju Guo, Department of Gastroenterology, Shenzhen Traditional Chinese Medicine Hospital, The Fourth Clinical Medical College of Guangzhou University of Chinese Medicine, No. 1 Fuhua Road, Futian, Shenzhen 518033, Guangdong Province, China. gsj1080@163.com
Key Words Spasmolytic polypeptide-expressing metaplasia; Gastric carcinogenesis; Gastric stem cells; Intestinal metaplasia; Cellular plasticity; Chronic inflammation
Core Tip Spasmolytic polypeptide-expressing metaplasia (SPEM) encompasses distinct injury-associated states in the gastric corpus. This review focuses on the stem/progenitor-cell origins and lineage plasticity of proliferative SPEM, comparing evidence for contributions from corpus isthmus stem/progenitor cells, the mucous neck–chief transitional lineage, and chief-cell-labeled populations. We distinguish transient repair-associated SPEM from persistent proliferative states associated with chronic inflammation, oncogenic signaling, intestinal differentiation, and dysplasia. Although SPEM is not an obligatory intermediate of gastric carcinogenesis, persistent proliferative SPEM is closely associated with progression-related changes. Reproducible pathological criteria and longitudinal human validation are required before proliferative SPEM can be incorporated into clinical risk stratification.
Citation Zhang WJ, Huang YZ, Chen Q, Zheng ST, Yuan HS, Chen XB, Liang YZ, Hong XX, Xu YF, Li HW, Gao Y, Guo SJ. Proliferative spasmolytic polypeptide-expressing metaplasia in gastric carcinogenesis: Stem cell origins, lineage plasticity, and clinical implications. World J Stem Cells 2026; In press
PDF 126709-in-press.pdf
Received
2026-08-11 07:31
Peer-Review Started
2026-08-11 07:31
First Decision by Editorial Office Director
Return for Revision
2026-08-25 08:26
Revised
2026-09-04 16:28
Publication Fee Transferred
2026-11-09 03:54
Second Decision by Editor
2026-11-13 03:14
Second Decision by Editor-in-Chief
Final Decision by Editorial Office Director
2026-11-13 10:27
Articles in Press
2026-11-13 10:27
Edit the Manuscript by Language Editor
Typeset the Manuscript
ISSN 1948-0210 (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 ©Author(s) (or their employer(s)) 2026. No commercial re-use. See Permissions. Published by Baishideng Publishing Group Inc.
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