Evidence map›Paper›PMID 40332226›Full record

ArticleInternational journal of molecular sciences2025

Integrating Machine Learning and Bulk and Single-Cell RNA Sequencing to Decipher Diverse Cell Death Patterns for Predicting the Prognosis of Neoadjuvant Chemotherapy in Breast Cancer.

Lingyan Xiang, Jiajun Yang, Jie Rao, Aolong Ma, Chen Liu, Yuqi Zhang, Aoling Huang, Ting Xie, Haochen Xue, Zhengzhuo Chen and 2 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

Lingyan XiangDepartment of Pathology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Jiajun YangDepartment of Pathology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Jie RaoDepartment of Pathology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Aolong MaDepartment of Pathology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Chen LiuDepartment of Pathology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Yuqi ZhangDepartment of Pathology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Aoling HuangDepartment of Pathology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Ting XieDepartment of Pathology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Haochen XueDepartment of Pathology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Zhengzhuo ChenDepartment of Pathology, Renmin Hospital of Wuhan University, Wuhan 430060, China.
Jingping YuanDepartment of Pathology, Renmin Hospital of Wuhan University, Wuhan 430060, China.ORCID 0000-0002-2922-4839
Honglin YanDepartment of Pathology, Renmin Hospital of Wuhan University, Wuhan 430060, China.ORCID 0000-0001-7645-9692

Funding

Natural Science Foundation of Hubei Province 2021CFB383The Sixth Round of Youth Key Talents Project of Renmin Hospital of Wuhan University RMQNZD2024046
6 · The paper itself

Abstract

Breast cancer (BRCA) continues to pose a serious risk to women's health worldwide. Neoadjuvant chemotherapy (NAC) is a critical treatment strategy. Nevertheless, the heterogeneity in treatment outcomes necessitates the identification of reliable biomarkers and prognostic models. Programmed cell death (PCD) pathways serve as a critical factor in tumor development and treatment response. However, the relationship between the diverse patterns of PCD and NAC in BRCA remains unclear. We integrated machine learning and multiple bioinformatics tools to explore the association between 19 PCD patterns and the prognosis of NAC within a cohort of 921 BRCA patients treated with NAC from seven multicenter cohorts. A prognostic risk model based on PCD-related genes (PRGs) was constructed and evaluated using a combination of 117 machine learning algorithms. Immune infiltration analysis, mutation analysis, pharmacological analysis, and single-cell RNA sequencing (scRNA-seq) were conducted to explore the genomic profile and clinical significance of these model genes in BRCA. Immunohistochemistry (IHC) was employed to validate the expression of select model genes (

Indexed as

Breast NeoplasmsMachine LearningSingle-Cell AnalysisBiomarkers, TumorCell DeathFemaleGene Expression Regulation, NeoplasticHumansMiddle AgedNeoadjuvant TherapyPrognosisSequence Analysis, RNABiomarkers, Tumorbreast cancerbulk and single-cell RNA sequencingmachine learningneoadjuvant chemotherapyprogrammed cell death

Identifiers

PMID40332226
PMCPMC12027272

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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.