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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 Clin Oncol. Jun 24, 2026; 17(6): 121469
Published online Jun 24, 2026. doi: 10.5306/wjco.121469
From residue to cancer risk: How thirdhand smoke drives cancer hallmarks
Jian-Hua Mao, Hang Chang
Jian-Hua Mao, Hang Chang, Division of Biological Systems and Engineering, Berkeley Biomedical Data Science Center, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, United States
Author contributions: Mao JH and Chang H planed the outline of the manuscript, wrote and edited the manuscript; all authors have read and approved the final manuscript.
AI contribution statement: After drafting this minireview, the authors used ChatGPT to refine the language and readability. The authors discussed the reviewers’ comment and together wrote the responses to these comments. Then we used ChatGPT to polish English. All original content was provided by the authors, who reviewed and edited the AI’s suggestions before final adoption. The authors take full responsibility for the content of the publication.
Supported by the University of California Tobacco Related Disease Research Program (UC TRDRP), No. T32PT6221.
Conflict-of-interest statement: All authors declare no conflict of interest in publishing the manuscript.
Corresponding author: Hang Chang, PhD, Principal Investigator, Division of Biological Systems and Engineering, Berkeley Biomedical Data Science Center, Lawrence Berkeley National Laboratory, 1 Cyclotron Road, Berkeley, CA 94720, United States. hchang@lbl.gov
Received: March 25, 2026
Revised: April 13, 2026
Accepted: June 2, 2026
Published online: June 24, 2026
Processing time: 89 Days and 14.5 Hours
Core Tip

Core Tip: Thirdhand smoke (THS) represents a persistent and underrecognized environmental carcinogen whose complex chemical mixture drives cancer-relevant biological processes beyond the window of active smoking. By integrating THS-induced molecular and cellular perturbations, such as DNA damage, epigenetic reprogramming, oxidative stress, and chronic inflammation, within the framework of the hallmarks of cancer, a systems-level paradigm for carcinogenic risk assessment emerges. This approach moves beyond traditional single-endpoint toxicology to capture the cumulative, multi-pathway impact of chronic low-dose exposures. Applying this framework to THS reveals how residual tobacco toxicants synergistically disrupt multiple cancer hallmarks, providing a mechanistically grounded basis for evaluating long-term cancer risk and informing environmental health policy.

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