Evidence map›Paper›PMID 34837916›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2021

Predictive Value of miR-146a rs2431697 Polymorphism to Myelofibrosis Progression in Patients with Myeloproliferative Neoplasm.

Salah Aref, Doaa Atia, Ahmed Al Tantawy, Mohamed Al Boghdady, Enas Gouda

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

5 citing papers in PubMed, 4 citations in OpenAlex.

  1. Deciphering the Inflammatory Network in Pediatric Recurrent Tonsillitis: The Role of TRAF6, IRAK1, and miR-146a-5p.Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery · 2026
    Article
  2. Review
  3. Article
  4. The Role of NLRP3, a Star of Excellence in Myeloproliferative Neoplasms.International journal of molecular sciences · 2023
    Review
  5. Review
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 1 institution in 1 country.

Salah ArefHematology Unit, Department of Clinical Pathology, Faculty of Medicine, Mansoura University, Egypt.ORCID 0000-0002-4822-5204
Doaa AtiaHematology Unit, Department of Clinical Pathology, Faculty of Medicine, Mansoura University, Egypt.
Ahmed Al TantawyMedical Oncology Unit, Mansoura University Oncology Center (MUOC) Mansoura University; Egypt.
Mohamed Al BoghdadyHematology Unit, Mansoura University Oncology Center (MUOC), Mansoura University, Egypt.
Enas GoudaHematology Unit, Department of Clinical Pathology, Faculty of Medicine, Mansoura University, Egypt.
Mansoura University · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBone marrow myelofibrosis (BMF) that develop on top of Polycythaemia vera (PV) and essential thrombocythemia leads to shortening of the patient's overall survival. This study aimed to address the impact of miR-146a rs2431697 polymorphism on inflammatory biomarkers and genes expression and the hazards of myelofibrosis progression. PATIENTS AND

methodsThe study included 88 myeloproliferative neoplasm (40 PV; 27 ET; 21 MF) and 90 healthy controls. For all investigated subjects miR-146a rs2431697 genotypes were identified by sequencing and the expression of miR-146a; IL-1β; NF-κB; a NOD-like receptor family, pyrin domain containing 3 (NLRP3) (NLRP3) genes were estimated by real time PCR.

resultsmiR146a genotypes revealed that there was significant association between TT and TC genotypes with MF. The degree of miR146a expression was significantly reduced in MF as compared to both PV and ET. In contrast; the levels of IL-1β; NF-κB; NLRP3 genes expression were significantly elevated in MF patients group as compared to PV and ET patients' group. Multivariate analysis identified TT genotype as poor predictor of MF progression.

conclusionmiR-146a rs2431697 TT genotype is associated with high risk of MF progression in MPN patients. Targeting of IL-1β; NF-κB; NLRP3 genes might help  in hindering of  MF progression in  MPN patients,<br />.

Indexed as

AgedBiomarkersBone Marrow NeoplasmsCase-Control StudiesDisease ProgressionFemaleGene ExpressionGenotypeHumansInterleukin-1betaMaleMicroRNAsMiddle AgedMyeloproliferative DisordersNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinBiomarkersIL1B protein, humanInterleukin-1betaMicroRNAsMIRN146 microRNA, humanNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanmiR-146aMPNMyelofibrosis

Identifiers

PMID34837916
PMCPMC9068196
OpenAlexW3215876444

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.