Evidence map›Paper›PMID 39730613›Full record

ArticleScientific reports2024

Prognostic model based on tumor stemness genes for triple-negative breast cancer.

Min Ouyang, Yajun Gui, Namei Li, Lin Zhao

Abstract read
In one paragraph

Article in Scientific reports, 2024. 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. Integrating multi-omics data for next-generation cancer research and precision medicine.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

4 authors.

Min OuyangDepartment of Pharmacy, The Second Xiangya Hospital, Central South University, Changsha, 410000, Hunan, China.
Yajun GuiDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, 410000, Hunan, China.
Namei LiDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, 410000, Hunan, China.
Lin ZhaoDepartment of Pathology, The Second Xiangya Hospital, Central South University, Changsha, 410000, Hunan, China. 508156@csu.edu.cn.

Funding

National Natural Science Foundation of China 82302873National Natural Science Foundation of China 82303258Natural Science Foundation of Hunan Province 2022JJ40686Natural Science Foundation of Hunan Province 2023JJ40874Scientific Research Launch Project for new employees of the Second Xiangya Hospital of Central South University QH20230202
6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is an aggressive disease with a poor prognosis and lack of effective treatment. In this study, TNBCs were analyzed from the perspective of tumor stemness based on scRNA-seq data. The analysis showed that tumor cells of TNBC were divided into 4 subtypes, with subtype 2 having the highest stemness score. A prognostic model of 7 tumor stemness-related genes (AP2S1, CHML, FABP7, FADS2, PAXX, SDC1 and TOP2A) was developed based on marker genes of this subtype and TCGA data, and the predictive power of this feature was well validated in different clinical subgroups. TNBC patients in the low TS group had a better prognosis. In addition, drug sensitivity analysis showed that patients in the high TS (tumor stemness) score group were more sensitive to PD-L1 inhibitors and the chemotherapeutic agents. In conclusion, our study developed a prognostic model based on TNBC tumor stemness cell marker genes, which has a good ability to predict the prognosis of TNBC patients and the effect of response to drug therapy.

Indexed as

Biomarkers, TumorNeoplastic Stem CellsTriple Negative Breast NeoplasmsFemaleGene Expression Regulation, NeoplasticHumansMiddle AgedPrognosisBiomarkers, TumorDrug responsePrognostic modelsPrognostic predictionsScRNATNBCTumor stemness

Identifiers

PMID39730613
PMCPMC11680876

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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.