Evidence map›Paper›PMID 32440325›Full record

ArticleIranian journal of basic medical sciences2020

Investigating the inhibitory effect of miR-34a, miR-449a, miR-1827, and miR-106b on target genes including NOTCH1, c-Myc, and CCND1 in human T cell acute lymphoblastic leukemia clinical samples and cell line.

Tohid Naderi, Samira Mohammadi-Yeganeh, Neda Mohammadi-Hezaveh, Razie Hadavi, Ahmad Gharehbaghian, Nader Vazifeh-Shiran, Vahid Fallah Azad, Mahdi Paryan

Open access · greenAbstract read
In one paragraph

Article in Iranian journal of basic medical sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 45% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. A Comprehensive Analysis of the Downregulation ofFrontiers in molecular biosciences · 2021
    Article
  4. 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

8 authors at 3 institutions in 1 country.

Tohid NaderiDepartment of Laboratory Hematology and Blood Bank, School of Allied Medicine, Shahid Beheshti University of medical sciences, Tehran, Iran.
Samira Mohammadi-YeganehMedical Nanotechnology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Neda Mohammadi-HezavehDepartment of Laboratory Hematology and Blood Bank, School of Allied Medicine, Shahid Beheshti University of medical sciences, Tehran, Iran.
Razie HadaviDepartment of Biochemistry, School of Medicine, Semnan University of Medical Sciences, Semnan, Iran.
Ahmad GharehbaghianDepartment of Laboratory Hematology and Blood Bank, School of Allied Medicine, Shahid Beheshti University of medical sciences, Tehran, Iran.
Nader Vazifeh-ShiranDepartment of Laboratory Hematology and Blood Bank, School of Allied Medicine, Shahid Beheshti University of medical sciences, Tehran, Iran.
Vahid Fallah AzadMahak Charity Hospital, Tehran, Iran.
Mahdi ParyanDepartment of Research and Development, Production and Research Complex, Pasteur Institute of Iran, Tehran, Iran.
Shahid Beheshti University of Medical Sciences · IRPasteur Institute of Iran · IRSemnan University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesmicroRNAs are small non-coding molecules that regulate gene expression in various biological processes. T-cell acute lymphoblastic leukemia (T-ALL) is a malignancy accompanied with genetic aberrations and accounts for 20% of children's and adult's ALL. Notch signaling pathway dysregulation occurs in 60% of T-ALL cases. In the present study, we aimed to determine the relationship between miRNAs and genes involved in Notch signaling pathway. MATERIALS AND

methodsConsidering the role of the pathway and its down-stream genes in proliferation, differentiation, cell cycle, and apoptosis,

resultsQuantitative Real-Time PCR indicated that

conclusionThese miRNAs can be proposed as biomarkers and new therapeutic targets in T-ALL patients who have

Indexed as

BioinformaticsBiomarkerleukemiamiRNANotch signaling pathway T-cell acute lymphoblastic

Identifiers

PMID32440325
PMCPMC7229500
OpenAlexW3002749298

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.