Evidence map›Paper›PMID 29562494›Full record

ArticleCancer biomarkers : section A of Disease markers2018

Aberrant expression of miR-141 and nuclear receptor small heterodimer partner in clinical samples of prostate cancer.

Maryam Khorasani, Ladan Teimoori-Toolabi, Taghi Naserpour Farivar, Mojgan Asgari, Maryam Abolhasani, Hossein Shahrokh, Ali Afgar, Elham Kalantari, Amir Peymani, Reza Mahdian

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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 34% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Expression of KIF18A Is Associated with Increased Tumor Stage and Cell Proliferation in Prostate Cancer.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  7. Review
  8. High Expression of KIF22/Kinesin-Like DNA Binding Protein (Kid) as a Poor Prognostic Factor in Prostate Cancer Patients.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Article
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

10 authors at 4 institutions in 1 country.

Maryam KhorasaniDepartment of Molecular Medicine, School of Medicine, Qazvin University of Medical Sciences, Qazvin, Iran.
Ladan Teimoori-ToolabiMolecular Medicine Department, Pasteur Institute of Iran, Tehran, Iran.
Taghi Naserpour FarivarMedical Microbiology Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
Mojgan AsgariOncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Maryam AbolhasaniOncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Hossein ShahrokhDepartment of Uro-oncology, Hasheminejad Kidney Center, Iran University of Medical Sciences, Tehran, Iran.
Ali AfgarMolecular Medicine Department, Pasteur Institute of Iran, Tehran, Iran.
Elham KalantariOncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Amir PeymaniMedical Microbiology Research Center, Qazvin University of Medical Sciences, Qazvin, Iran.
Reza MahdianMolecular Medicine Department, Pasteur Institute of Iran, Tehran, Iran.
Iran University of Medical Sciences · IRPasteur Institute of Iran · IRQazvin University of Medical Sciences · IRHasheminejad Kidney Center · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProstate cancer (PCa) is the second most common cancer in men worldwide. Currently, prostate-specific antigen (PSA) test and digital rectal exam are the main screening tests used for PCa diagnosis. However, due to the low specificity of these tests, new alternative biomarkers such as deregulated RNAs and microRNAs have been implemented.

objectivesAberrant expressions of small heterodimer partner gene (SHP, NR0B2) and mir-141 are reported in various cancers. The aim of this study was to investigate the SHP and miR-141 expression level in tissue samples of prostate cancer.

methodsThe expression level of SHP gene and miR-141 was assessed by real time PCR and their relative amounts were calculated by the Δ⁢ΔCT method. Also, IHC technique was used to determine the expression level of SHP protein.

resultsThe miR-141 was significantly up-regulated in the samples of metastatic tumors compared to localized tumor samples (P< 0.001, 31.17-fold change). Tumor samples showed lower SHP mRNA expression levels than BPH samples (p= 0.014, 4.7-fold change). The results of paired t-test analysis showed there was no significant difference between the SHP gene expression in PCa samples and their matched tumor-adjacent normal tissue (p= 0.5).

conclusionsThe data obtained in our study confirm the involvement of miR-141 in PCa progression and metastasis. These effects could be mediated by AR via down-regulation of its co-repressor protein, i.e., SHP.

Indexed as

Disease ProgressionHumansImmunohistochemistryMaleMicroRNAsProstatic NeoplasmsReceptors, Cytoplasmic and NuclearUp-RegulationMicroRNAsMIRN141 microRNA, humannuclear receptor subfamily 0, group B, member 2Receptors, Cytoplasmic and Nuclearbiomarkergene expressionImmunohistochemistrymiR-141nuclear receptorsProstate cancerSHP gene

Identifiers

PMID29562494
PMCPMC13078446
OpenAlexW2790047680

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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.