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Copyright: ©Author(s) 2026. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution-NonCommercial (CC BY-NC 4.0) license. No commercial re-use. See permissions. Published by Baishideng Publishing Group Inc.
World J Gastrointest Oncol. Apr 15, 2026; 18(4): 116504
Published online Apr 15, 2026. doi: 10.4251/wjgo.v18.i4.116504
Digital polymerase chain reaction detection of telomerase reverse transcriptase promoter mutations in hepatitis B virus related hepatocellular carcinoma
Shuai Shao, Yu Xiong, Mo-Wei Kong, Yang Yu, Chun-Xiang Zhang
Shuai Shao, Yu Xiong, Mo-Wei Kong, Yang Yu, Chun-Xiang Zhang, Department of Cardiology, The Affiliated Hospital of Southwest Medical University, Luzhou 646000, Sichuan Province, China
Co-first authors: Shuai Shao and Yu Xiong.
Co-corresponding authors: Yang Yu and Chun-Xiang Zhang.
Author contributions: Shao S and Kong MW wrote the manuscript; Yu Y and Zhang CX provided crucial suggestions, guidance for the writing, and they contributed equally to this manuscript and are co-corresponding authors; Xiong Y reviewed and revised the manuscript; Shao S and Xiong Y contributed equally to this manuscript and are co-first authors. All authors read and approved the final manuscript.
Conflict-of-interest statement: All the authors report no relevant conflicts of interest for this article.
Corresponding author: Chun-Xiang Zhang, MD, PhD, Professor, Department of Cardiology, The Affiliated Hospital of Southwest Medical University, No. 25 Taiping Street, Luzhou 646000, Sichuan Province, China. zhangchx999@163.com
Received: November 13, 2025
Revised: January 9, 2026
Accepted: January 23, 2026
Published online: April 15, 2026
Processing time: 146 Days and 19.1 Hours
Core Tip

Core Tip: This study provides the first systematic evidence that an optimized digital polymerase chain reaction assay can achieve ultra-sensitive detection of the guanine-cytosine-rich telomerase reverse transcriptase (TERT) promoter C228T mutation in hepatitis B virus-related hepatocellular carcinoma, with 100% sensitivity and a detection limit of 0.55 cp/μL - far surpassing traditional sequencing methods. By integrating TERT mutation status with clinical variables, we developed a prognostic nomogram that accurately predicts overall and disease-free survival, enabling early recurrence detection through ctDNA-based liquid biopsy. This work bridges molecular mechanism and clinical translation, establishing TERT mutation detection by digital polymerase chain reaction as a cornerstone technology for precision hepatocarcinology and individualized postoperative surveillance.