Evidence map›Paper›PMID 40346580›Full record

ArticleJournal of experimental & clinical cancer research : CR2025

Tumor cell-intrinsic BIN1 deficiency promotes the immunosuppression and impedes ferroptosis of non-small cell lung cancer via G3BP1-mediated degradation of STAT1.

Jiali Wang, Yunlong Jia, Tianxu Liu, Xinyan Liu, Shuxian Yin, Jiaqi Chen, Xiaoqing Xu, Yi Zhang, Lihua Liu

Abstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

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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

9 authors.

Jiali WangDepartment of Tumor Immunotherapy, Hebei Medical University Fourth Affiliated Hospital and Hebei Provincial Tumor Hospital, Shijiazhuang, 050035, P.R. China.
Yunlong JiaDepartment of Tumor Immunotherapy, Hebei Medical University Fourth Affiliated Hospital and Hebei Provincial Tumor Hospital, Shijiazhuang, 050035, P.R. China.
Tianxu LiuDepartment of Tumor Immunotherapy, Hebei Medical University Fourth Affiliated Hospital and Hebei Provincial Tumor Hospital, Shijiazhuang, 050035, P.R. China.
Xinyan LiuDepartment of Tumor Immunotherapy, Hebei Medical University Fourth Affiliated Hospital and Hebei Provincial Tumor Hospital, Shijiazhuang, 050035, P.R. China.
Shuxian YinDepartment of Tumor Immunotherapy, Hebei Medical University Fourth Affiliated Hospital and Hebei Provincial Tumor Hospital, Shijiazhuang, 050035, P.R. China.
Jiaqi ChenDepartment of Tumor Immunotherapy, Hebei Medical University Fourth Affiliated Hospital and Hebei Provincial Tumor Hospital, Shijiazhuang, 050035, P.R. China.
Xiaoqing XuDepartment of General Surgery, Xuanwu Hospital Capital Medical University, Beijing, 100053, China.
Yi ZhangBiotherapy Center and Cancer Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, 450002, China.
Lihua LiuDepartment of Tumor Immunotherapy, Hebei Medical University Fourth Affiliated Hospital and Hebei Provincial Tumor Hospital, Shijiazhuang, 050035, P.R. China. cdlihualiu@hebmu.edu.cn.

Funding

Clinical Research and Innovation Team Support Program of Hebei Medical University 2022LCTD-A11Medical Science Research Project of Hebei 20210168S&T program of Hebei H2024206222
6 · The paper itself

Abstract

backgroundTumors often evade immune surveillance by limiting T cell infiltration. In non-small cell lung cancer (NSCLC), increased infiltration of CD8

methodsTo investigate the relationship between BIN1 expression and CD8

resultsWe observed that BIN1 expression is downregulated in NSCLC tumor tissues, with its reduced expression strongly associated with advanced disease progression and poor prognosis. Bioinformatics analysis of immune infiltration in human NSCLC samples revealed a positive correlation between BIN1 expression in NSCLC tissues and CD8

conclusionThis study highlights the crucial role of the BIN1/G3BP1/STAT1/CD8

Indexed as

Adaptor Proteins, Signal TransducingCarcinoma, Non-Small-Cell LungDNA HelicasesFerroptosisLung NeoplasmsSTAT1 Transcription FactorTumor Suppressor ProteinsAnimalsCD8-Positive T-LymphocytesCell Line, TumorFemaleHumansLymphocytes, Tumor-InfiltratingMaleMiceNuclear ProteinsAdaptor Proteins, Signal TransducingBIN1 protein, humanDNA HelicasesNuclear ProteinsSTAT1 protein, humanSTAT1 Transcription FactorTumor Suppressor ProteinsBIN1CD8+ T cellFerroptosisImmune escapeNon-small cell lung cancer

Identifiers

PMID40346580
PMCPMC12063428

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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 OpenQuestion graph.