Evidence map›Paper›PMID 41413360›Full record

ArticleNPJ breast cancer2025

PARG inhibition suppresses breast cancer progression and potentiates immunoresponse through MTDH degradation mediated by E3 ligase ITCH-dependent ubiquitination.

Junnai Wang, Yanhua Dong, Weiwei Lun, Manman Nai, Yajing Shi, Jianfang Geng, Wenhui Cai, Jiaxi Liu, Hongyu Li, Lei Li

Abstract read
In one paragraph

Article in NPJ breast cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Redefining breast cancer: therapeutic opportunities in HER2-low and emerging molecular subtypes.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
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.

Junnai Wang *Department of Gynecology, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Yanhua Dong *Department of Gynecology, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Weiwei LunDepartment of Reproductive Immunity Center, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Manman NaiDepartment of Gynecology, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Yajing ShiDepartment of Research Center, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Jianfang GengDepartment of Research Center, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Wenhui CaiDepartment of Reproductive Immunity Center, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Jiaxi LiuDepartment of Gynecology, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Hongyu LiDepartment of Gynecology, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China. fuliuzhongdianshiyanshi@gs.zzu.edu.cn.
Lei LiDepartment of Gynecology, Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China. sfylilei@zzu.edu.cn.

Funding

he Key projects of high schools in Henan Province 24A320036the Henan Province Science and Technology Tackling Plan Key Projects Co-constructed by Province and Ministry SBGJ202402067
6 · The paper itself

Abstract

PARG plays an important role in cancer progression and immunoresponse, but its role in breast cancer is not yet fully elucidated. The advanced breast cancer is still a persistent challenge in clinical oncology. Despite the encouraging progress made in cancer immunotherapy, its efficacy is still limited by tumor malignancy and the immunosuppressive microenvironment. Through comprehensive proteomic analysis employing liquid chromatography-tandem mass spectrometry, we identified ITCH-a HECT-family E3 ubiquitin ligase-as a novel interaction partner of PARG. Co-immunoprecipitation and ubiquitination assays revealed that the PARG inhibition markedly enhances the PARylation of the E3 ubiquitin ligase ITCH. This triggers its autoubiquitination-dependent activation, after which activated ITCH catalyzes the ubiquitination of the oncoprotein metadherin (MTDH). This ultimately leads to MTDH's proteasomal degradation and the consequent suppression of tumor growth. Importantly, RNA immunoprecipitation analysis further demonstrated that PARGi-induced ITCH/MTDH potentiates the MHC-I antigen presentation machinery in tumor cells, which correlates with increased infiltration of cytotoxic T lymphocytes within the tumor microenvironment. In invivo validation, combinatorial therapy using the selective PARG inhibitor COH34 with anti-PD-L1 immune checkpoint blockade demonstrated synergistic therapeutic efficacy in a murine breast cancer model. To the best of our knowledge, PARG inhibition plays an important role in limiting cancer progression and potentiating immune response, depending on its regulatory function in PARylation and ubiquitination in breast cancer.

Identifiers

PMID41413360
PMCPMC12714780

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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.