Evidence map›Paper›PMID 40541964›Full record

ArticleCell death & disease2025

ISCU-p53 axis orchestrates macrophage polarization to dictate immunotherapy response in esophageal squamous cell carcinoma.

Jialiang Luo, Xu Zhang, Zhicheng Liang, WeiTao Zhuang, Mingxin Jiang, Min Ma, Shuying Peng, Shujie Huang, Guibin Qiao, Qingyun Chen

Abstract read
In one paragraph

Article in Cell death & disease, 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.

  1. Trial
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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

10 authors.

Jialiang Luo *Institute of Medical Research, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China.ORCID http://orcid.org/0000-0003-0070-4131
Xu Zhang *Department of Thoracic Surgery, State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China.
Zhicheng LiangDepartment of Immunology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.
WeiTao ZhuangDepartment of Medical Oncology, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, China.
Mingxin JiangDepartment of Medical Laboratory, School of Laboratory Medicine and Biotechnology, Southern Medical University, Guangzhou, Guangdong, China.
Min MaSchool of Medicine, South China University of Technology, Guangzhou, Guangdong, China.
Shuying PengDepartment of Medical Laboratory, School of Laboratory Medicine and Biotechnology, Southern Medical University, Guangzhou, Guangdong, China.
Shujie HuangDepartment of Thoracic Surgery, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China.
Guibin QiaoDepartment of Thoracic Surgery, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong, China. qiaoguibin@smu.edu.cn.ORCID http://orcid.org/0000-0001-9200-9317
Qingyun ChenInstitute of Medical Research, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou, Guangdong, China. chenqingyun@gdph.org.cn.ORCID http://orcid.org/0000-0002-9726-8403

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82173083National Natural Science Foundation of China (National Science Foundation of China) 82303982National Natural Science Foundation of China (National Science Foundation of China) 82472751Natural Science Foundation of Guangdong Province (Guangdong Natural Science Foundation) 2022A1515012579
6 · The paper itself

Abstract

Immunological heterogeneity in esophageal squamous cell carcinoma (ESCC) poses a significant challenge to the efficacy and response to immunotherapy. In this study, we used single-cell RNA sequencing to uncover substantial heterogeneity in the tumor microenvironments (TMEs) among patients received PD-1 inhibitor with partial response (PR), stable disease (SD), and that who underwent surgery without prior therapy. Notably, tumors classified as SD demonstrated an immunosuppressive environment, characterized by a higher prevalence of M2-like macrophages and lower frequencies of T and B cells, especially PD1

Indexed as

Esophageal NeoplasmsEsophageal Squamous Cell CarcinomaImmunotherapyIron-Sulfur ProteinsMacrophagesTumor Suppressor Protein p53AnimalsFemaleHumansMiceTumor MicroenvironmentIron-Sulfur ProteinsTumor Suppressor Protein p53

Identifiers

PMID40541964
PMCPMC12181301

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Registered trials

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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.