Evidence map›Paper›PMID 38084438›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

G3BP1 and SLU7 Jointly Promote Immune Evasion by Downregulating MHC-I via PI3K/Akt Activation in Bladder Cancer.

Xianchong Zheng, Jiawei Chen, Minhua Deng, Kang Ning, Yulu Peng, Zhenhua Liu, Xiangdong Li, Zhaohui Zhou, Huancheng Tang, Yaoying Li and 2 more

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
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

36 citing papers in PubMed, 25 citations in OpenAlex.

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  19. Overcoming resistance to anti-PD-1/PD-L1 therapy in cancer.Cancer drug resistance (Alhambra, Calif.) · 2026
    Review
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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

12 authors at 1 institution in 1 country.

Xianchong ZhengDepartment of Urology, Sun Yat-sen University Cancer Center, Guangzhou, 510060, P. R. China.ORCID 0000-0002-8005-6519
Jiawei ChenDepartment of Urology, Sun Yat-sen University Cancer Center, Guangzhou, 510060, P. R. China.
Minhua DengDepartment of Urology, Sun Yat-sen University Cancer Center, Guangzhou, 510060, P. R. China.
Kang NingDepartment of Urology, Sun Yat-sen University Cancer Center, Guangzhou, 510060, P. R. China.
Yulu PengDepartment of Urology, Sun Yat-sen University Cancer Center, Guangzhou, 510060, P. R. China.
Zhenhua LiuDepartment of Urology, Sun Yat-sen University Cancer Center, Guangzhou, 510060, P. R. China.
Xiangdong LiDepartment of Urology, Sun Yat-sen University Cancer Center, Guangzhou, 510060, P. R. China.
Zhaohui ZhouDepartment of Urology, Sun Yat-sen University Cancer Center, Guangzhou, 510060, P. R. China.
Huancheng TangDepartment of Urology, Sun Yat-sen University Cancer Center, Guangzhou, 510060, P. R. China.
Yaoying LiState Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center, Guangzhou, 510060, P. R. China.
Tiebang KangState Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center, Guangzhou, 510060, P. R. China.
Zhuowei LiuDepartment of Urology, Sun Yat-sen University Cancer Center, Guangzhou, 510060, P. R. China.ORCID 0000-0002-8159-3033
Sun Yat-sen University · CN

Funding

Cancer Innovative Research Program of Sun Yat-sen University Cancer Center CIRP-SYSUCC-0014Guangdong Basic and Applied Basic Research Foundation 2022A1515111119Guangzhou Municipal Science and Technology Project 202201011026National Natural Science Foundation of China 82002666National Natural Science Foundation of China 82073103National Natural Science Foundation of China 82103264
6 · The paper itself

Abstract

Immune checkpoint inhibitors (ICIs) show promise as second-line treatment for advanced bladder cancer (BLCA); however, their responsiveness is limited by the immune evasion mechanisms in tumor cells. This study conduct a Cox regression analysis to screen mRNA-binding proteins and reveals an association between Ras GTPase-activating protein-binding protein 1 (G3BP1) and diminished effectiveness of ICI therapy in patients with advanced BLCA. Subsequent investigation demonstrates that G3BP1 enhances immune evasion in BLCA cells by downregulating major histocompatibility complex class I (MHC-I) through phosphoinositide 3-kinase (PI3K)/Akt signaling activation. Mechanistically, G3BP1 interacts with splicing factor synergistic lethal with U5 snRNA 7 (SLU7) to form a complex with poly(A)-binding protein cytoplasmic 1 and eukaryotic translation initiation factor 4 gamma 1. This complex stabilizes the closed-loop structure of the mRNAs of class IA PI3Ks and consequently facilitates their translation and stabilization, thereby activating PI3K/Akt signaling to downregulate MHC-I. Consistently, targeting G3BP1 with epigallocatechin gallate (EGCG) impedes immune evasion and sensitizes BLCA cells to anti-programmed cell death (PD)-1 antibodies in mice. Thus, G3BP1 and SLU7 collaboratively contribute to immune evasion in BLCA, indicating that EGCG is a precision therapeutic agent to enhance the effectiveness of anti-PD-1 therapy.

Indexed as

DNA HelicasesUrinary Bladder NeoplasmsAnimalsCarrier ProteinsHumansImmune EvasionMicePhosphatidylinositol 3-KinasePhosphatidylinositol 3-KinasesPoly-ADP-Ribose Binding ProteinsProto-Oncogene Proteins c-aktRNA HelicasesRNA Recognition Motif ProteinsRNA Splicing FactorsCarrier ProteinsDNA HelicasesG3BP1 protein, humanPhosphatidylinositol 3-KinasePhosphatidylinositol 3-KinasesPoly-ADP-Ribose Binding ProteinsProto-Oncogene Proteins c-aktRNA HelicasesRNA Recognition Motif ProteinsRNA Splicing FactorsSLU7 protein, humanSLU7 protein, mousebladder cancerepigallocatechin gallateimmune checkpoint inhibitorsimmune evasionmajor histocompatibility complex class IRas GTPase-activating protein-binding protein 1

Identifiers

PMID38084438
PMCPMC10870071
OpenAlexW4389607467

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.