Evidence map›Paper›PMID 39285160›Full record

ArticleCell discovery2024

Targeting SNRNP200-induced splicing dysregulation offers an immunotherapy opportunity for glycolytic triple-negative breast cancer.

Wenxiao Yang, Luo Hong, Linwei Guo, Yunjin Wang, Xiangchen Han, Boyue Han, Zheng Xing, Guoliang Zhang, Hongxia Zhou, Chao Chen and 3 more

Abstract read
In one paragraph

Article in Cell discovery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Neurodegenerative spliceosomopathies.Frontiers in cell and developmental biology · 2026
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Non-Coding RNAs in Breast Cancer: Diagnostic and Therapeutic Implications.International journal of molecular sciences · 2024
    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

13 authors.

Wenxiao Yang *Precision Cancer Medicine Center, Fudan University Shanghai Cancer Center, Shanghai, China.
Luo Hong *Precision Cancer Medicine Center, Fudan University Shanghai Cancer Center, Shanghai, China.
Linwei Guo *Precision Cancer Medicine Center, Fudan University Shanghai Cancer Center, Shanghai, China.
Yunjin WangPrecision Cancer Medicine Center, Fudan University Shanghai Cancer Center, Shanghai, China.
Xiangchen HanPrecision Cancer Medicine Center, Fudan University Shanghai Cancer Center, Shanghai, China.
Boyue HanPrecision Cancer Medicine Center, Fudan University Shanghai Cancer Center, Shanghai, China.
Zheng XingPrecision Cancer Medicine Center, Fudan University Shanghai Cancer Center, Shanghai, China.
Guoliang ZhangPrecision Cancer Medicine Center, Fudan University Shanghai Cancer Center, Shanghai, China.
Hongxia ZhouPrecision Cancer Medicine Center, Fudan University Shanghai Cancer Center, Shanghai, China.
Chao ChenPrecision Cancer Medicine Center, Fudan University Shanghai Cancer Center, Shanghai, China.
Hong LingDepartment of Breast Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Zhimin ShaoPrecision Cancer Medicine Center, Fudan University Shanghai Cancer Center, Shanghai, China.
Xin HuPrecision Cancer Medicine Center, Fudan University Shanghai Cancer Center, Shanghai, China. xinhu@fudan.edu.cn.ORCID http://orcid.org/0000-0002-8160-8362

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81872137National Natural Science Foundation of China (National Science Foundation of China) 82072917National Natural Science Foundation of China (National Science Foundation of China) 82272957National Natural Science Foundation of China (National Science Foundation of China) 82303735Shanghai Science and Technology Development Foundation (Shanghai Science and Technology Development Fund) 22DZ2204400
6 · The paper itself

Abstract

Metabolic dysregulation is prominent in triple-negative breast cancer (TNBC), yet therapeutic strategies targeting cancer metabolism are limited. Here, utilizing multiomics data from our TNBC cohort (n = 465), we demonstrated widespread splicing deregulation and increased spliceosome abundance in the glycolytic TNBC subtype. We identified SNRNP200 as a crucial mediator of glucose-driven metabolic reprogramming. Mechanistically, glucose induces acetylation at SNRNP200 K1610, preventing its proteasomal degradation. Augmented SNRNP200 then facilitates splicing key metabolic enzyme-encoding genes (GAPDH, ALDOA, and GSS), leading to increased lactic acid and glutathione production. Targeting SNRNP200 with antisense oligonucleotide therapy impedes tumor metabolism and enhances the efficacy of anti-PD-1 therapy by activating intratumoral CD8

Identifiers

PMID39285160
PMCPMC11405407

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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.