Evidence map›Paper›PMID 40281780›Full record

ArticleBioengineering (Basel, Switzerland)2025

Leveraging Diverse Cell-Death Patterns to Decipher the Interactive Relation of Unfavorable Outcome and Tumor Microenvironment in Breast Cancer.

Yue Li, Ting Ding, Tong Zhang, Shuangyu Liu, Jinhua Wang, Xiaoyan Zhou, Zeqi Guo, Qian He, Shuqun Zhang

Abstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 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

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

1 citing paper in PubMed.

  1. 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

9 authors.

Yue LiDepartment of Clinical Laboratories, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.ORCID 0000-0002-1129-4572
Ting DingDepartment of Clinical Laboratories, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.
Tong ZhangDepartment of Clinical Laboratories, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.
Shuangyu LiuDepartment of Clinical Laboratories, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.
Jinhua WangDepartment of Clinical Laboratories, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.
Xiaoyan ZhouDepartment of Clinical Laboratories, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.
Zeqi GuoDepartment of Clinical Laboratories, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.
Qian HeDepartment of Clinical Laboratories, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.ORCID 0000-0003-3744-8805
Shuqun ZhangDepartment of Oncology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China.ORCID 0000-0002-6998-7849

Funding

Hospital research supporting funds from The Second Affiliated Hospital of Xi'an Jiaotong Uni-versity. N/A
6 · The paper itself

Abstract

backgroundProgrammed cell death (PCD) dynamically influences breast cancer (BC) prognosis through interactions with the tumor microenvironment (TME). We investigated 13 PCD patterns to decipher their prognostic impact and mechanistic links to TME-driven outcomes. Our study aimed to explore the complex mechanisms underlying these interactions and establish a prognostic prediction model for breast cancer.

methodsUsing TCGA and METABRIC datasets, we integrated single-sample gene set enrichment analysis (ssGSEA), weighted gene co-expression network analysis (WGCNA), and Least Absolute Shrinkage and Selection Operator (LASSO) to explore PCD-TME interactions. Multi-dimensional analyses included immune infiltration, genomic heterogeneity, and functional pathway enrichment.

resultsOur results indicated that high apoptosis and pyroptosis activity, along with low autophagy, correlated with favorable prognosis, which was driven by enhanced anti-tumor immunity, including more M1 macrophage polarization and activated CD8+ T cells in TME. PCD-related genes could promote tumor metastasis and poor prognosis via VEGF/HIF-1/MAPK signaling and immune response, including Th1/Th2 cell differentiation, while new tumor event occurrences (metastasis/secondary cancers) were linked to specific clinical features and gene mutation spectrums, including TP53/CDH1 mutations and genomic instability. We constructed a six-gene LASSO model (

conclusionOur study provided a comprehensive landscape of the cancer survival difference and related PCD-TME interaction axis and highlighted that high-apoptosis/pyroptosis states caused favorable prognosis, underlying mechanisms closely related with the TME where anti-tumor immunity would be beneficial for patient prognosis. These findings highlighted the model's potential for risk stratification in BC.

Indexed as

breast cancerimmune microenvironmentmachine learningnew neoplasm occurrenceprogrammed cell deathtumor prognosis

Identifiers

PMID40281780
PMCPMC12024675

What Socratic holds

Textmetadata
LicenceCC BY
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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.