Evidence map›Paper›PMID 35937944›Full record

ArticleDisease markers2022

Establishment and Analysis of an Individualized EMT-Related Gene Signature for the Prognosis of Breast Cancer in Female Patients.

Wei Xue, Chenyu Sun, Hui Yuan, Xin Yang, Qiuping Zhang, Yunnuo Liao, Hongwei Guo

Abstract read
In one paragraph

Article in Disease markers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. EMT and cancer: what clinicians should know.Nature reviews. Clinical oncology · 2025
    Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
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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

7 authors.

Wei XueGuangxi Key Laboratory for Research and Evaluation of Bioactive Molecules& College of Pharmacy, Guangxi Medical University, Nanning 530021, China.ORCID https://orcid.org/0000-0001-6089-8041
Chenyu SunAMITA Health Saint Joseph Hospital Chicago, 2900 N. Lake Shore Drive, Chicago, 60657 Illinois, USA.ORCID https://orcid.org/0000-0003-3812-3164
Hui YuanPublic Health Center, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, 710061, China.
Xin YangKey Laboratory of Longevity and Aging-Related Diseases of Chinese Ministry of Education & Center for Translational Medicine, Guangxi Medical University, Nanning 530021, China.
Qiuping ZhangKey Laboratory of Longevity and Aging-Related Diseases of Chinese Ministry of Education & Center for Translational Medicine, Guangxi Medical University, Nanning 530021, China.
Yunnuo LiaoGuangxi Key Laboratory for Research and Evaluation of Bioactive Molecules& College of Pharmacy, Guangxi Medical University, Nanning 530021, China.
Hongwei GuoGuangxi Key Laboratory for Research and Evaluation of Bioactive Molecules& College of Pharmacy, Guangxi Medical University, Nanning 530021, China.ORCID https://orcid.org/0000-0002-4046-2643

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The current high mortality rate of female breast cancer (BC) patients emphasizes the necessity of identifying powerful and reliable prognostic signatures in BC patients. Epithelial-mesenchymal transition (EMT) was reported to be associated with the development of BC. The purpose of this study was to identify prognostic biomarkers that predict overall survival (OS) in female BC patients by integrating data from TCGA database. Method: We first downloaded the dataset in TCGA and identified gene signatures by overlapping candidate genes. Differential analysis was performed to find differential EMT-related genes. Univariate regression analysis was then performed to identify candidate prognostic variables. We then developed a prognostic model by multivariate analysis to predict OS. Calibration curves, receiver operating characteristics (ROC) curves, Result: In this study, we identified and validated a prognostic model integrating age and six genes (CD44, P3H1, SDC1, COL4A1, TGF Conclusion: This study offered a robust predictive model for OS prediction in female BC patients and may provide a more accurate treatment strategy and personalized therapy in the future.

Indexed as

Breast NeoplasmsEpithelial-Mesenchymal TransitionFemaleHumansPrognosisProportional Hazards ModelsROC Curve

Identifiers

PMID35937944
PMCPMC9352481

What OpenQuestion holds

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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.