Schlafen 11 as a predictive biomarker and therapeutic target in cancer: From mechanisms to clinical application

The emergence of chemotherapy resistance remains a pivotal challenge in oncology, driving the search for robust biomarkers of drug sensitivity. Schlafen 11 (SLFN11) is well established as a predictive biomarker for the response to DNA-damaging agents; however, its clinical translation is hindered by key challenges. This review systematically synthesizes current evidence on SLFN11, detailing its structure, multifaceted mechanisms, dynamic expression patterns, and epigenetic regulation. We evaluate detection methodologies, highlight the promise of dynamic monitoring via liquid biopsy, and explore rational combination therapies designed to leverage SLFN11 function. Finally, we provide a forward-looking perspective on integrating SLFN11 into biomarker-driven strategies and outline the clinical validation required to realize its full potential in precision oncology.

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Publication Details

Journal
Drug Discovery Today
Published
2025-12-08
DOI
https://doi.org/10.1016/j.drudis.2025.104579
Primary Topic
PARP inhibition in cancer therapy
Type
article
Field-Weighted Citation Impact
0.00
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article

Schlafen 11 as a predictive biomarker and therapeutic target in cancer: From mechanisms to clinical application

Xiang Wang, Kang Liu, Dan Zhang, Shuang Xu et al.
Drug Discovery Today
PARP inhibition in cancer therapy
article

Schlafen 11 as a predictive biomarker and therapeutic target in cancer: From mechanisms to clinical application

Xiang Wang, Kang Liu, Dan Zhang, Shuang Xu, Ying Luo, Nengming Lin
article en

Abstract

The emergence of chemotherapy resistance remains a pivotal challenge in oncology, driving the search for robust biomarkers of drug sensitivity. Schlafen 11 (SLFN11) is well established as a predictive biomarker for the response to DNA-damaging agents; however, its clinical translation is hindered by key challenges. This review systematically synthesizes current evidence on SLFN11, detailing its structure, multifaceted mechanisms, dynamic expression patterns, and epigenetic regulation. We evaluate detection methodologies, highlight the promise of dynamic monitoring via liquid biopsy, and explore rational combination therapies designed to leverage SLFN11 function. Finally, we provide a forward-looking perspective on integrating SLFN11 into biomarker-driven strategies and outline the clinical validation required to realize its full potential in precision oncology.

Drug Discovery TodayVol. 31(1)
Westlake University (CN), Affiliated Hangzhou First People's Hospital, Westlake University, School of Medicine (CN)
Openalex Percentile: Top 45%
PARP inhibition in cancer therapy
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