Evidence mapPaperPMID 41706757Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

PRELID1 and VDAC3 Coordinate a Senescence-Like State in Germinal Center B Cells to Promote IL-7-Driven Antitumor Immunity in Colorectal Cancer.

Yuhan Liao, Huimeng Xu, Xinghua Zhuo, Shupeng Hu, Lanhui Huang, Zhe Hao, Jianxiong Chen, Yulu Wang, Jun Zhou

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. 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

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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

9 authors.

Yuhan LiaoDepartment of Pathology, Nanfang Hospital, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.
Huimeng XuDepartment of Pathology, Nanfang Hospital, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.
Xinghua ZhuoDepartment of Pathology, Nanfang Hospital, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.
Shupeng HuSchool of Computer Science, Guangdong Polytechnic Normal University, Guangzhou, China.
Lanhui HuangDepartment of Pathology, Nanfang Hospital, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.
Zhe HaoDepartment of Pathology, Nanfang Hospital, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.
Jianxiong ChenDepartment of Pathology, The Tenth Affiliated Hospital (Dongguan People's Hospital), Southern Medical University, Dongguan, China.
Yulu WangDepartment of Pathology, Nanfang Hospital, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.
Jun ZhouDepartment of Pathology, Nanfang Hospital, School of Basic Medical Sciences, Southern Medical University, Guangzhou, Guangdong, China.ORCID https://orcid.org/0000-0003-0272-8807

Funding

National Natural Science Foundation of China 81272763National Natural Science Foundation of China 81672466National Natural Science Foundation of China 81972334National Natural Science Foundation of China 82173297National Natural Science Foundation of China 82273351National Natural Science Foundation of China 82373066Natural Science Foundation of Guangdong Province 2017A030313550Natural Science Foundation of Guangdong Province 2019A1515011205Natural Science Foundation of Guangdong Province 2023A1515010329
6 · The paper itself

Abstract

Colorectal cancer (CRC) is characterized by an immune-suppressive microenvironment that facilitates to tumor progression and immunotherapy resistance. Emerging evidence indicates that tumor-infiltrating B cell subsets play dual roles in modulating antitumor immunity. However, the mechanisms underlying their regulatory functions remain poorly understood. In this study, we constructed single-cell transcriptomic analyses and a Bgc adoptive transfer model in B cell-deficient mice, performing multifaceted validation to confirm that targeting the PRELID1-VDAC3-IL-7 axis in senescence-like germinal center B cells enhances sensitivity to anti-PD-L1 immunotherapy. Mechanistically, we identify a senescence-like state in germinal center B cells (Bgc) that enhances antitumor immunity in CRC by promoting Interleukin-7 (IL-7) secretion and alleviating CD8

Indexed as

B-LymphocytesColorectal NeoplasmsGerminal CenterInterleukin-7Mitochondrial Membrane Transport ProteinsAnimalsCD8-Positive T-LymphocytesCellular SenescenceHumansMiceMice, Inbred C57BLTumor MicroenvironmentInterleukin-7Mitochondrial Membrane Transport Proteinscancer microenvironmentcellular senescencecolorectal cancerimmune checkpoint blockademitochondria‐lysosome interactions

Identifiers

PMID41706757
PMCPMC13104075

What Socratic holds

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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 Socratic graph.