Evidence map›Paper›PMID 29995098›Full record

ArticleClinics (Sao Paulo, Brazil)2018

Expression of tumor suppressors miR-195 and let-7a as potential biomarkers of invasive breast cancer.

Marcia M Marques, Adriane F Evangelista, Taciane Macedo, René Aloisio da Costa Vieira, Cristovam Scapulatempo-Neto, Rui M Reis, André L Carvalho, Ismael Dale Cotrim Guerreiro da Silva

Abstract read
In one paragraph

Article in Clinics (Sao Paulo, Brazil), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Review
  3. Mechanism of salidroside in tumor suppression through the miRNA-mRNA signaling axis.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2024
    Review
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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.

Marcia M MarquesCentro de Pesquisa em Oncologia Molecular (CPOM), Hospital de Cancer de Barretos, Barretos, SP, BR.
Adriane F EvangelistaCentro de Pesquisa em Oncologia Molecular (CPOM), Hospital de Cancer de Barretos, Barretos, SP, BR.
Taciane MacedoCentro de Pesquisa em Oncologia Molecular (CPOM), Hospital de Cancer de Barretos, Barretos, SP, BR.
René Aloisio da Costa VieiraDepartamento de Mastologia e Reconstrucao Mamaria, Hospital de Cancer de Barretos, Barretos, SP, BR.
Cristovam Scapulatempo-NetoDepartamento de Patologia, Hospital de Cancer de Barretos, Barretos, SP, BR.
Rui M ReisCentro de Pesquisa em Oncologia Molecular (CPOM), Hospital de Cancer de Barretos, Barretos, SP, BR.
André L CarvalhoCentro de Pesquisa em Oncologia Molecular (CPOM), Hospital de Cancer de Barretos, Barretos, SP, BR.
Ismael Dale Cotrim Guerreiro da SilvaDepartamento de Ginecologia, Universidade Federal de Sao Paulo, Sao Paulo, SP, BR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveMicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression at the posttranscriptional level. Some miRNAs, including let-7a and miR-195, have been described as tumor suppressors. However, the roles of these microRNAs in breast cancer progression remain controversial. The aim of this study is to evaluate miR-195 and let-7a expression as potential biomarkers of invasive breast cancer.

methodsIn the present study, 200 individuals were separated into three groups: (i) 72 women constituting the control group who were selected according to rigorous and well-established criteria; (ii) 56 patients with benign breast tumors; and (iii) 72 patients with malignant breast cancers of different clinical stages. The miR-195 and let-7a expression levels in serum were evaluated by real-time PCR. The results were assessed alone and in combination, and the analysis included an estimation of sensitivity and specificity in ROC curves.

resultsCompared with the benign and control groups, both microRNAs were downregulated in the malignant breast cancer patient group. Compared with the malignant group, the combination of both biomarkers in the control and benign groups showed good sensitivity and specificity in the serum with AUCs of 0.75 and 0.72, respectively. The biomarker combination for the control group versus the malignant group exhibited a better sensitivity and specificity than for the benign group versus the malignant group.

conclusionThese findings support the evidence that the analysis of miR-195 and let-7a can be used as a non-invasive biomarker for breast cancer detection.

Indexed as

AdultAgedAnalysis of VarianceBiomarkers, TumorBreast NeoplasmsCarcinogenesisCase-Control StudiesDown-RegulationFemaleGene Expression Regulation, NeoplasticHumansLogistic ModelsMicroRNAsMiddle AgedNeoplasm InvasivenessNeoplasm StagingBiomarkers, TumorMicroRNAsMIRN195 microRNA, humanmirnlet7 microRNA, human

Identifiers

PMID29995098
PMCPMC6024513

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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.