Evidence map›Paper›PMID 35117330›Full record

ArticleTranslational cancer research2020

Analyzing the key gene expression and prognostics values for acute myeloid leukemia.

Lingling Shi, Yan Huang, Xunjun Huang, Weijie Zhou, Jie Wei, Donghong Deng, Yongrong Lai

Open access · diamondAbstract read
In one paragraph

Article in Translational cancer research, 2020. 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
0.8field-weighted citation impact, top 25% 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, 14 citations in OpenAlex.

  1. Current issues in molecular biology · 2025
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  8. Cancer-Associated Dysregulation of Sumo Regulators: Proteases and Ligases.International journal of molecular sciences · 2022
    Review
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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

7 authors at 3 institutions in 1 country.

Lingling Shi *Department of Hematology, the First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Yan Huang *Department of Hematology and Rheumatology, People's Hospital of Baise, Baise, China.
Xunjun HuangDepartment of Hematology and Rheumatology, People's Hospital of Baise, Baise, China.
Weijie ZhouDepartment of Hematology and Rheumatology, People's Hospital of Baise, Baise, China.
Jie WeiDepartment of Hematology and Rheumatology, People's Hospital of Baise, Baise, China.
Donghong DengDepartment of Hematology, the First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Yongrong LaiDepartment of Hematology, the First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Baise University · CNFirst Affiliated Hospital of GuangXi Medical University · CNGuangxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute myeloid leukemia (AML) is one of the first tumor types sequenced at the whole genome level. However, numbers of the mutated genes expression levels, functions, and prognostics values still unclear.

methodsTo most ordinary mutated genes were analyzed via cancer virtual cohort discovery analysis platform (CVCDAP), and further investigated the mutational conversions, variant allele frequencies (VAF), driver genes, and potential druggable mutated genes in AML. The top mutated gene mRNA expression levels and the relationship between gene expression levels and prognosis for AML patients were performed by Gene Expression Profiling Interactive Analysis (GEPIA). Moreover, we used the UALCAN dataset to confirm the association between gene expression levels and prognosis for AML patients. Enrichment functions of the top mutated genes of AML were analyzed through Metascape. Finally, the role of these defined genes in cancer pathways and potential drug targets were analyzed by gene set cancer analysis (GSCALite).

resultsThe top 20 mutated genes for AML included

conclusionsPresent study showed overexpression of FLT3, ABCA6, and PCLO indicated the poor prognosis of AML, but overexpression of SLIT3 and HSP3 functioned as an AML protector. There are several drugs and small molecules that target the top 20 mutated genes in AML.

Indexed as

Acute myeloid leukemia (AML)bioinformatics analysistop mutated genes

Identifiers

PMID35117330
PMCPMC8797974
OpenAlexW3108184491

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.