Evidence map›Paper›PMID 40624348›Full record

ArticleDiscover oncology2025

Multi-omics analysis of the effects of pla2g4a on the prognosis of various cancers and its experimental validation in breast cancer cell lines.

Yao Qian, Quan Yuan, Hao Yu, Rongjie Ye, Ming Niu, Feng Liu

Abstract read
In one paragraph

Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Decoding the breast cancer microenvironment by spatial multi-omics: from architecture to clinical translation.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  4. Article
  5. Article
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

6 authors.

Yao Qian *Department of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150000, Heilongjiang, China.
Quan Yuan *Department of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150000, Heilongjiang, China.
Hao Yu *Department of Hepato-Biliary-Pancreatic and Vascular Surgery, School of Medicine, The First Affiliated Hospital of Xiamen University, Xiamen University, Xiamen, 361000, Fujian, China.
Rongjie YeDepartment of Orthopaedics, Quanzhou First Hospital Affiliated to Fujian Medical University, Quanzhou, 362000, Fujian, China.
Ming NiuDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150000, Heilongjiang, China. niuming2024@126.com.
Feng LiuDepartment of Breast Surgery, Harbin Medical University Cancer Hospital, Harbin, 150000, Heilongjiang, China. LiuFeng3061@163.com.

Funding

Beijing Heart to Heart Foundation HXXT2021ktyj002Beijing Science and Technology Medical Development Foundation KC2021-JF-0055-05Haiyan Science Foundation JJMS2022-08
6 · The paper itself

Abstract

backgroundPlatelet-related exosomes (PREs) are microparticles secreted by platelets into the bloodstream and are implicated in various cancer processes. This study aims to identify critical genes involved in Breast Cancer (BC)-associated PREs and to evaluate their role in cancer prognosis. PLA2G4A was identified as a key gene through the use of machine learning techniques and various genomic analyses, providing a foundation for precision medicine in BC treatment.

methodsDownload cancer-related data from databases such as UCSC Xena and ExMdb, use LASSO Cox regression and various machine learning algorithms to screen genes associated with BC survival, and perform functional and pathway enrichment analysis. The expression, immune relevance, diagnostic efficacy, and drug sensitivity of the PLA2G4A gene in pan-cancer and BC were specifically analyzed. The function of PLA2G4A in BC was validated through experiments, and its drug response and molecular docking were predicted using various databases and software tools.

resultsMachine learning methods and LASSO Cox regression were applied to analyze the relationship between gene expression and BC survival. PLA2G4A was identified as a key gene associated with cancer prognosis, supported by analyses of differential gene expression, survival outcomes, single nucleotide variations (SNVs), and copy number variations (CNVs). Biological pathway analyses through KEGG, GO, and GSEA highlighted PLA2G4A's involvement in key cancer-related processes. In vitro studies, including cell scratch assays, Transwell migration assays, and EdU proliferation tests, demonstrated that overexpression of PLA2G4A inhibited the proliferation and migration of BC cells.

conclusionsPLA2G4A plays a crucial role in the progression of BC, acting as a potential tumor-suppressor gene. The findings support its potential as a prognostic biomarker and further investigation is needed to explore its therapeutic potential in clinical settings.

Indexed as

BioinformaticsBreast neoplasmCancerMachine learningPLA2G4APlatelet-related exosomes

Identifiers

PMID40624348
PMCPMC12234970

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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.