Evidence map›Paper›PMID 40531330›Full record

ReviewCancer chemotherapy and pharmacology2025

From predictive biomarker to therapeutic target: the dual role of SLFN11 in chemotherapy sensitivity.

Yue Feng, Yingze Li, Zhenhao Zhang, Yuxuan Dai, Xingchun Gou, Kejing Lao, Running Zhang

Abstract readReviewLetter
PubMed Publisher
In one paragraph

Review in Cancer chemotherapy and pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Yue FengSchool of Clinical Medicine, Shaanxi University of Chinese Medicine, No.1 Century Road, Qindu District, Xianyang, 712046, China.
Yingze LiShaanxi Key Laboratory of Brain Disorders & Institute of Basic and Translational Medicine, Xi'an Medical University, No.1 Xinwang Road, Xi'an, 710021, China.
Zhenhao ZhangShaanxi Key Laboratory of Brain Disorders & Institute of Basic and Translational Medicine, Xi'an Medical University, No.1 Xinwang Road, Xi'an, 710021, China.
Yuxuan DaiShaanxi Key Laboratory of Brain Disorders & Institute of Basic and Translational Medicine, Xi'an Medical University, No.1 Xinwang Road, Xi'an, 710021, China.
Xingchun GouShaanxi Key Laboratory of Brain Disorders & Institute of Basic and Translational Medicine, Xi'an Medical University, No.1 Xinwang Road, Xi'an, 710021, China.
Kejing LaoShaanxi Key Laboratory of Brain Disorders & Institute of Basic and Translational Medicine, Xi'an Medical University, No.1 Xinwang Road, Xi'an, 710021, China. laokejing_jzs@xiyi.edu.cn.
Running ZhangSecond Department of Encephalopathy, The Second Affiliated Hospital of Shaanxi University of Chinese Medicine, Xiangyang, 712046, China. xyzrn2000@163.com.

Funding

Natural Science Basic Research Program of Shaanxi Province 2024JC-YBMS-726Open Program for College Students of Xi'an Medical University 2024DXS04Science and Technology Innovation Base-Open and Sharing Platform Resources Project of Shaanxi Province 2024CX-GXPT-08Scientific Research Program Funded by Shaanxi Provincial Education Department 23JP152Shaanxi Province Innovation Talent Promotion Program 2023KJXX-066Young Talent Fund of Association for Science and Technology in Shaanxi 20220610
6 · The paper itself

Abstract

SLFN11, a DNA/RNA helicase implicated in replication stress response, has recently emerged as a pivotal determinant of chemotherapy sensitivity across multiple cancer types. The expression level of SLFN11 in various cancers is significantly positively correlated with the sensitivity of cancer cell DNA damage agents. SLFN11 exerts its chemosensitizing effects by RPA-coated single-stranded DNA (ssDNA) at stressed replication forks at stalled replication forks, thereby potentiating the cytotoxicity of platinum agents, topoisomerase inhibitors, and PARP inhibitors. Its roles in inhibiting ATR translation, mediating p53-independent apoptosis, sensitizing towards IFN-γ and enhancing chromatin accessibility also remain investigational. The down-regulation of SLFN11 expression is associated with epigenetic silencing including promoter methylation, histone deacetylation, and the histone methylation. In this paper, we reviewed the recent progress of SLFN11 as predictive biomarker and therapeutic target in multiple cancers including medulloblastoma, prostate cancer, breast cancer, ovarian cancer, lung cancer, head and neck cancer, esophageal carcinoma, gastric carcinoma and colorectal cancer. We also summarized 10 active clinical trials conducting molecular analyses to assess SLFN11's role. By bridging mechanistic understanding with translational opportunities, this review provides a roadmap for leveraging SLFN11 to overcome chemoresistance and advance precision oncology.

Indexed as

Antineoplastic AgentsBiomarkers, TumorNeoplasmsNuclear ProteinsAnimalsDNA DamageDrug Resistance, NeoplasmHumansMolecular Targeted TherapyAntineoplastic AgentsBiomarkers, TumorNuclear ProteinsSLFN11 protein, humanBiomarkerCancersDDAsDrug resistanceSLFN11Therapeutic target

Identifiers

PMID40531330

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.