Evidence map›Paper›PMID 34264524›Full record

ArticleJournal of clinical laboratory analysis2021

Potential value of circulatory microRNA10b gene expression and its target E-cadherin as a prognostic and metastatic prediction marker for breast cancer.

Fatma Ibrahim Dwedar, Reham Said Shams-Eldin, Salwa Nayer Mohamed, Ayman Farouk Mohammed, Salwa Hamdi Gomaa

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Fatma Ibrahim DwedarDepartment of Medical Biochemistry, Faculty of Medicine, Alexandra University, Alexandria, Egypt.
Reham Said Shams-EldinDepartment of Medical Biochemistry, Faculty of Medicine, Alexandra University, Alexandria, Egypt.
Salwa Nayer MohamedDepartment of Cancer management and Research, Medical Research Institute, Alexandria University, Alexandria, Egypt.
Ayman Farouk MohammedDepartment of Clinical and Experimental Surgery, Medical Research Institute, Alexandria University, Alexandria, Egypt.
Salwa Hamdi GomaaDepartment of Chemical pathology, Medical Research Institute, Alexandria University, Alexandria, Egypt.ORCID https://orcid.org/0000-0002-4447-7498
Alexandria University · EGBibliotheca Alexandrina · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBreast cancer (BC) is the leading cause of cancer death in women worldwide. Most BC studies on candidate microRNAs were tissue specimen based. Recently, there has been a focus on the study of cell-free circulating miRNAs as promising biomarkers in (BC) diagnosis and prognosis. Therefore, we aimed to investigate the circulating levels of miR-10b and its target soluble E- cadherin as potentially easily accessible biomarkers for breast cancer.

methodsSixty-one breast cancer patients and forty-eight age- and sex-matched healthy volunteers serving as a control group were enrolled in the present study. Serum samples were used to assess miRNA10b expression by TaqMan miRNA assay technique. In addition, soluble E-cadherin expression level in serum was determined using ELISA technique.

resultCirculating miR-10b expression level and serum sE-cadherin was significantly upregulated in patients with BC compared to controls. Moreover, serum miR-10b displayed progressive up-regulation in advanced stages with higher level in metastatic compared to non-metastatic BC. Additionally, the combined use of both serum miR-10b and sE-cadherin revealed the highest sensitivity and specificity for detection of BC metastasis (92.9% and 97.9% respectively) with an area under curve (AUC) of 0.98, 95% CI (0.958-1.00).

conclusionOur data suggest that circulating miR-10b could be utilized as a potential non-invasive serum biomarker for diagnosis and prognosis of breast cancer with better performance to predict BC metastasis achieved on measuring it simultaneously with serum sE-cadherin. Further studies with a large cohort of patients are warranted to validate the serum biomarker for breast cancer management.

Indexed as

AdultAgedAntigens, CDBiomarkers, TumorBreast NeoplasmsCadherinsCase-Control StudiesCirculating MicroRNAFemaleGene Expression Regulation, NeoplasticHumansMembrane GlycoproteinsMiddle AgedPrognosisReceptors, ImmunologicROC CurveAntigens, CDBiomarkers, TumorCadherinsCDH1 protein, humanCirculating MicroRNALILRB2 protein, humanMembrane GlycoproteinsReceptors, Immunologicbreast cancercirculating miR-10bnon-invasive biomarkersoluble E-cadherinTaqMan miRNA assay

Identifiers

PMID34264524
PMCPMC8373345
OpenAlexW3180011724

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Registered trials

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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.