Evidence map›Paper›PMID 40217479›Full record

ArticleBMC cancer2025

Comprehensive analysis of metabolism-related gene biomarkers reveals their impact on the diagnosis and prognosis of triple-negative breast cancer.

Weibin Ren, Yuyun Yu, Tao Wang, Xueyao Wang, Kunkai Su, Yanbo Wang, Wenjie Tang, Miaomiao Liu, Yanhui Zhang, Long Yang and 1 more

Abstract read
In one paragraph

Article in BMC cancer, 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. 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

11 authors.

Weibin RenJinan Microecological Biomedicine Shandong Laboratory, Jinan, 250117, Shandong, China.
Yuyun YuThe First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Tao WangJinan Microecological Biomedicine Shandong Laboratory, Jinan, 250117, Shandong, China.
Xueyao WangJinan Microecological Biomedicine Shandong Laboratory, Jinan, 250117, Shandong, China.
Kunkai SuJinan Microecological Biomedicine Shandong Laboratory, Jinan, 250117, Shandong, China.
Yanbo WangJinan Microecological Biomedicine Shandong Laboratory, Jinan, 250117, Shandong, China.
Wenjie TangJinan Microecological Biomedicine Shandong Laboratory, Jinan, 250117, Shandong, China.
Miaomiao LiuJinan Microecological Biomedicine Shandong Laboratory, Jinan, 250117, Shandong, China.
Yanhui ZhangJinan Microecological Biomedicine Shandong Laboratory, Jinan, 250117, Shandong, China.
Long YangJinan Microecological Biomedicine Shandong Laboratory, Jinan, 250117, Shandong, China.
Hongyan DiaoJinan Microecological Biomedicine Shandong Laboratory, Jinan, 250117, Shandong, China. diao.hy@163.com.

Funding

Jinan Microecological Biomedicine Shandong Laboratory JNL-2022001AResearch Project of Jinan Microecological Biomedicine Shandong Laboratory JNL-2023008QShandong Provincial Laboratory Project SYS202202Youth Foundation of Shandong Natural Science Foundation ZR2024QH318
6 · The paper itself

Abstract

backgroundTriple-negative breast cancer (TNBC) is an aggressive subtype of breast cancer characterized by poor prognosis and limited treatment options, which underscores the urgency of the discovery of new biomarkers. Metabolic reprogramming is a hallmark of cancer and is expected to serve as a strong predictive biomarker for breast cancer.

methodsWe integrated RNA expression data and clinical information from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases to explore the associations between metabolism-related gene expression and TNBC prognosis. Our comprehensive approach included differential expression analysis, enrichment analysis, Cox regression analysis, machine learning, and in vitro experimental validation.

resultsWe identified five pivotal genes-SDS, RDH12, IDO1, GLDC, and ALOX12B-that were significantly correlated with the prognosis of TNBC patients. A prognostic model incorporating these genes was developed and validated in an independent patient cohort. The model demonstrated predictive validity, as TNBC patients classified into the high-risk group exhibited significantly poorer prognoses. Additionally, utilizing the risk model, we evaluated the mutational landscape, immune infiltration, immunotherapy response, and drug sensitivity in TNBC, providing insights into potential therapeutic strategies.

conclusionsThis study established a robust prognostic model capable of accurately predicting clinical outcomes and metastasis, which could aid in personalized clinical decision-making.

Indexed as

Biomarkers, TumorTriple Negative Breast NeoplasmsFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansIndoleamine-Pyrrole 2,3,-DioxygenasePrognosisBiomarkers, TumorIDO1 protein, humanIndoleamine-Pyrrole 2,3,-DioxygenaseDrug sensitivityImmune infiltrationMetabolic signaturesPrognosticTriple-negative breast cancer (TNBC)

Identifiers

PMID40217479
PMCPMC11987350

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.