Evidence map›Paper›PMID 29843213›Full record

ArticleCancer biomarkers : section A of Disease markers2018

Clinical potential of miR-940 as a diagnostic and prognostic biomarker in breast cancer patients.

Wenjun Liu, Yongmei Xu, Hongliang Guan, Hongwei Meng

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

30 citing papers in PubMed.

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  4. JHDM1D-AS1-driven inhibition of miR-940 releases ARTN expression to induce breast carcinogenesis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
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  11. DecreasedTranslational lung cancer research · 2021
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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.

Wenjun LiuDepartment of Breast and Thyroid Surgery, Shanxian Central Hospital, Heze 274300, Shandong, China.
Yongmei XuDepartment of Breast and Thyroid Surgery, Shanxian Central Hospital, Heze 274300, Shandong, China.
Hongliang GuanDepartment of Breast and Thyroid Surgery, Shanxian Central Hospital, Heze 274300, Shandong, China.
Hongwei MengDepartment of Internal Medicine, Shanxian Central Hospital, Heze 274300, Shandong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer remains the most invasive female malignancy worldwide. Functional role of microRNA-940 (miR-940) have been investigated in various cancer. The purpose of this study was to assess the serum miR-940 expression and its clinical significance in breast cancer.

methodsExpression of miR-940 was measured by quantitative real-time polymerase chain reaction (qRT-PCR). The diagnostic value of miR-940 was analyzed with receiver operating characteristics (ROC) analysis. To explore the prognostic performance of miR-940, Kaplan-Meier survival assay and Cox regression analysis were performed.

resultsDownregulated miR-940 was detected in the breast cancer patients compared with the healthy controls (P< 0.001). The miR-940 expression was correlated with lymph node metastasis (P= 0.014) and TNM stage (P= 0.003). The area under the ROC curve (AUC) was 0.905, with sensitivity and specificity of 94.5% and 78.6%. From the survival curves, patients with low miR-940 expression had poor overall survival compare with those with high expression (log-rank P= 0.009). The Cox analysis indicated that miR-940 was an independent prognostic factor (HR = 2.645, 95% CI = 1.426-4.906 and P= 0.002). Decreased miR-940 expression was also been found in triple-negative breast cancer (TNBC) samples, and might predict poor prognosis in TNBC patients.

conclusionsSerum downregulated miR-940 may serve as a reliable diagnostic and prognostic biomarker in breast cancer patients.

Indexed as

Biomarkers, TumorAdultAgedArea Under CurveBreast NeoplasmsFemaleHumansKaplan-Meier EstimateMicroRNAsMiddle AgedNeoplasm GradingNeoplasm StagingPrognosisProportional Hazards ModelsROC CurveBiomarkers, TumorMicroRNAsMIRN940 microRNA, humanbreast cancerdiagnosisMiR-940prognosis

Identifiers

PMID29843213
PMCPMC13078465

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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.