Evidence map›Paper›PMID 33243739›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2020

[RUNX1 gene mutations are associated with adverse prognosis of patients with acute myeloidleukemia].

Yanli Yang, Tiantian Li, Yinghua Geng, Jun Li

Open access · greenAbstract read
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 48% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

4 authors at 1 institution in 1 country.

Yanli YangDepartment of Hematology, First Affiliated Hospital of Bengbu Medical College, Bengbu 233000, China.
Tiantian LiDepartment of Hematology, First Affiliated Hospital of Bengbu Medical College, Bengbu 233000, China.
Yinghua GengDepartment of Hematology, First Affiliated Hospital of Bengbu Medical College, Bengbu 233000, China.
Jun LiDepartment of Hematology, First Affiliated Hospital of Bengbu Medical College, Bengbu 233000, China.
Bengbu Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore the rate and distribution of Runt- related transcription factor 1 (RUNX1) gene mutations in patients with acute myeloid leukemia (AML) and the correlation of these mutations with the clinical characteristics and survival outcomes of the patients.

methodsThe genomic DNA extracted from the bone marrow of 158 patients with newly diagnosed AML for PCR amplification of RUNX1 gene and sequence analysis to identify the mutations. The mutations of ASXL1, DNMT3A, TET2, FLT3, CEBPA, NPM1, IDH2, NRAS and c-KIT genes were also examined to analyze their association with RUNX1 gene mutations.

resultsAmong the 158 AML patients, 19 (12.0%) were found to have RUNX1 mutations in A166G (9 cases), A142T (6 cases) and A162L (4 cases). RUNX1 mutations were more frequent in elderly patients (

conclusionsRUNX1 gene mutations are associated with an adverse prognosis of patients with AML.

Indexed as

Leukemia, Myeloid, AcuteCore Binding Factor Alpha 2 SubunitHumansMutationNucleophosminPrognosisRemission InductionCore Binding Factor Alpha 2 SubunitNPM1 protein, humanNucleophosminRUNX1 protein, humanacute myeloid leukemiagene mutationRUNX1 gene

Identifiers

PMID33243739
PMCPMC7704376
OpenAlexW3107642539

What OpenQuestion holds

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Registered trials

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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.