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Publication Name World Journal of Gastrointestinal Oncology
Manuscript ID 123088
DOI 10.4251/wjgo.123088
Country China
Category Oncology
Manuscript Type Retrospective Study
Article Title Relationship of TRAP1, HMGB1, and p62 expression with clinicopathologic features in colon cancer tissues
Manuscript Source Unsolicited Manuscript
All Author List Hai-Long Guo, Yun-Peng Qi, Qiang Zhang, Jian-Jun Hao, Yu Yang, Ming-Yang Zhang and Zhen-Tao He
Funding Agency and Grant Number
Corresponding Author Zhen-Tao He, Academic Fellow, Department of General Surgery I, Third Affiliated Hospital of Qiqihar Medical University, No. 27 Taishun Street, Tiefeng District, Qiqihar 161000, Heilongjiang Province, China. hezhentao1983@qmu.edu.cn
Key Words Colon cancer; TRAP1; HMGB1; P62; Immunohistochemistry; Reverse transcription-polymerase chain reaction; Prognosis
Core Tip This study investigated the expression of TRAP1, HMGB1, and p62 in colon cancer tissues, all of which were significantly upregulated compared with adjacent normal mucosa at both protein and mRNA levels. Their high expressions were closely associated with adverse clinicopathological features including poor differentiation, lymph node metastasis, and advanced TNM stage. TRAP1 was identified as an independent predictor for lymph node metastasis and poor overall survival, showing superior prognostic value. HMGB1 also independently predicted lymph node metastasis, while p62 was correlated with tumor progression but lacked independent prognostic significance. These findings suggest that TRAP1, HMGB1, and p62 serve as promising biomarkers for colon cancer, with TRAP1 being particularly valuable for prognostic assessment.
Citation Guo HL, Qi YP, Zhang Q, Hao JJ, Yang Y, Zhang MY, He ZT. Relationship of TRAP1, HMGB1, and p62 expression with clinicopathologic features in colon cancer tissues. World J Gastrointest Oncol 2026; In press
PDF 123088-in-press.pdf
Received
2026-05-09 10:59
Peer-Review Started
2026-05-09 10:59
First Decision by Editorial Office Director
2026-05-27 01:47
Return for Revision
2026-05-27 01:47
Revised
2026-06-08 11:24
Publication Fee Transferred
2026-06-17 05:33
Second Decision by Editor
2026-07-28 02:34
Second Decision by Editor-in-Chief
Final Decision by Editorial Office Director
2026-07-28 13:01
Articles in Press
2026-07-28 13:01
Edit the Manuscript by Language Editor
Typeset the Manuscript
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/
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