Evidence map›Paper›PMID 42724479›Full record

ArticleTranslational cancer research2026

Network toxicology and interpretable modeling identify nicotine-associated neuroendocrine targets and a three-gene prognostic signature in breast cancer.

Junyan Weng, Caifeng Ou, Jiamin Yi, Huan Yang, Chiwei Chen, Mei Huang

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Article in Translational cancer research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Junyan Weng *Department of Breast, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.
Caifeng Ou *Department of Breast Care Surgery, The First Affiliated Hospital/The First Clinical Medicine School of Guangdong Pharmaceutical University, Guangzhou, China.
Jiamin YiThe First Clinical Medical School of Guangzhou University of Chinese Medicine, Guangzhou, China.
Huan YangThe First Clinical Medical School of Guangzhou University of Chinese Medicine, Guangzhou, China.
Chiwei Chen *Department of Breast, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.ORCID https://orcid.org/0000-0002-7719-032X
Mei Huang *Department of Breast, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.ORCID https://orcid.org/0009-0007-1164-0512

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Nicotine, a major tobacco metabolite and persistent environmental pollutant, is epidemiologically associated with breast cancer risk, yet its non-classical carcinogenic molecular mechanisms and prognostic value remain unclear. This study was designed to systematically elucidate the potential targets and molecular mechanisms underlying the prognostic impact of nicotine on breast cancer, alongside developing an interpretable prognostic risk model. Methods: This study integrated network toxicology, interpretable modeling, and molecular docking. Potential nicotine targets were intersected with breast cancer differentially expressed genes, and hub genes were identified via protein-protein interaction (PPI) network. A prognostic model was built using Cox regression analysis and interpreted by the SHapley Additive exPlanations (SHAP). The binding potential of nicotine to targets was predicted through in silico molecular docking. Results: Thirty-three nicotine-breast cancer common targets and 21 hub genes were identified. A three-gene prognostic model ( Conclusions: This study computationally prioritized potential nicotine-associated breast cancer targets and constructed a three-gene prognostic model; in silico docking analysis suggested the potential binding of nicotine to these targets. We hypothesize that nicotine might function as a potential neuroendocrine disruptor to modulate breast cancer progression via GPCR signaling pathways. We propose a unique nicotine-associated three-GPCR-gene signature that provides new clues for environmental health risk assessment and prognostic biomarker development in breast cancer, yet further experimental validation is needed.

Indexed as

Breast cancermolecular dockingnetwork toxicologynicotinepredictive model

Identifiers

PMID42724479
PMCPMC13559631

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