Evidence map›Paper›PMID 32497068›Full record

ArticlePloS one2020

Peripheral blood transcriptome identifies high-risk benign and malignant breast lesions.

Hong Hou, Yali Lyu, Jing Jiang, Min Wang, Ruirui Zhang, Choong-Chin Liew, Binggao Wang, Changming Cheng

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 21% of its field
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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  3. Reports of practical oncology and radiotherapy : journal of Greatpoland Cancer Center in Poznan and Polish Society of Radiation Oncology · 2024
    Article
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  5. Review
  6. [miR-16-5p regulates apoptosis and migration of drug-resistant breast cancer cells by targeting YWHAQ].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2022
    Article
  7. Article
  8. The regulation of PBXs and their emerging role in cancer.Journal of cellular and molecular medicine · 2022
    Review
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  10. 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

8 authors at 2 institutions in 3 countries.

Hong HouQingdao Central Hospital/Qingdao Cancer Hospital, Qingdao, Shandong Province, People's Republic of China.
Yali LyuHuaxia Bangfu Technology Incorporated, Beijing, People's Republic of China.
Jing JiangQingdao Lianchi Maternity and Infant Hospital, Qingdao, Shandong Province, People's Republic of China.
Min WangHuaxia Bangfu Technology Incorporated, Beijing, People's Republic of China.
Ruirui ZhangHuaxia Bangfu Technology Incorporated, Beijing, People's Republic of China.
Choong-Chin LiewGolden Health Diagnostics Incorporated, Jiangsu, People's Republic of China.ORCID 0000-0002-9908-0391
Binggao WangQingdao Central Hospital/Qingdao Cancer Hospital, Qingdao, Shandong Province, People's Republic of China.
Changming ChengHuaxia Bangfu Technology Incorporated, Beijing, People's Republic of China.
Qingdao University · CNBrigham and Women's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPeripheral blood transcriptome profiling is a potentially important tool for disease detection. We utilize this technique in a case-control study to identify candidate transcriptomic biomarkers able to differentiate women with breast lesions from normal controls.

methodsWhole blood samples were collected from 50 women with high-risk breast lesions, 57 with breast cancers and 44 controls (151 samples). Blood gene expression profiling was carried out using microarray hybridization. We identified blood gene expression signatures using AdaBoost, and constructed a predictive model differentiating breast lesions from controls. Model performance was then characterized by AUC sensitivity, specificity and accuracy. Biomarker biological processes and functions were analyzed for clues to the pathogenesis of breast lesions.

resultsTen gene biomarkers were identified (YWHAQ, BCLAF1, WSB1, PBX2, DDIT4, LUC7L3, FKBP1A, APP, HERC2P2, FAM126B). A ten-gene panel predictive model showed discriminatory power in the test set (sensitivity: 100%, specificity: 84.2%, accuracy: 93.5%, AUC: 0.99). These biomarkers were involved in apoptosis, TGF-beta signaling, adaptive immune system regulation, gene transcription and post-transcriptional protein modification.

conclusionA promising method for the detection of breast lesions is reported. This study also sheds light on breast cancer/immune system interactions, providing clues to new targets for breast cancer immune therapy.

Indexed as

Models, GeneticTranscriptomeAdultAgedArea Under CurveBiomarkers, TumorBreast NeoplasmsCase-Control StudiesData AccuracyEarly Detection of CancerFemaleHumansMiddle AgedRetrospective StudiesSensitivity and SpecificityYoung AdultBiomarkers, Tumor

Identifiers

PMID32497068
PMCPMC7272048
OpenAlexW3033765035

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.