Evidence map›Paper›PMID 31686732›Full record

ArticleIndian journal of clinical biochemistry : IJCB2019

Evaluation of the Expression Level and Hormone Receptor Association of miR-126 in Breast Cancer.

Maedeh Rouigari, Moein Dehbashi, Hossein Tabatabaeian, Kamran Ghaedi, Parisa Mohammadynejad, Mansoureh Azadeh

Open access · bronzeAbstract read
In one paragraph

Article in Indian journal of clinical biochemistry : IJCB, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

11 citing papers in PubMed, 18 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

6 authors at 3 institutions in 1 country.

Maedeh RouigariDepartment of Biology, Faculty of Basic Sciences, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran.
Moein Dehbashi2Division of Genetics, Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran.
Hossein Tabatabaeian2Division of Genetics, Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran.
Kamran Ghaedi4Division of Cellular and Molecular Biology, Department of Biology, Faculty of Sciences, University of Isfahan, Hezar Jerib Ave., Azadi Sq., Isfahan, 81746-73441 Iran.
Parisa MohammadynejadDepartment of Biology, Faculty of Basic Sciences, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran.
Mansoureh AzadehZist Fanavari Novin Biotechnology Institute, Isfahan, Iran.
University of Isfahan · IRIslamic Azad University of Shahrekord · IRAgricultural Biotechnology Research Institute of Iran · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is a major cause of cancer-related death in women worldwide. miRNAs are new players of breast tumorigenesis, used as diagnostic and prognostic biomarkers. Among various miRNAs, miR-126 has been proposed to have a tumor suppressive role in HER2 positive cancer. However, to have a better understanding of its role, further validation is required. The aim of this study was evaluating miR-126 expression level in breast cancer tissues and investigating its potential association with HER2, estrogen and progesterone receptors. miR-126 expression level was measured in 108 specimens including 78 malignant and 30 normal samples using RT-qPCR. The outcome was statistically analyzed. In silico studies were performed to find the potential mechanism of action, through which miR-126 imposes its function. Down-regulation of miR-126 was observed in tumor samples, as compared to the matched normal tissues. Down-regulation of miR-126 was also associated significantly with the absence of estrogen receptor in malignant samples. No association between miR-126 expression and HER2 status was observed. Our in silico analyses showed the possible role of Crk, PI

Indexed as

Breast cancerEstrogen receptorHER-2miR-126Progesterone receptor

Identifiers

PMID31686732
PMCPMC6801275
OpenAlexW2807758107

What OpenQuestion holds

Textmetadata
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.