Evidence map›Paper›PMID 35682627›Full record

ReviewInternational journal of molecular sciences2022

Molecular Classification and Overcoming Therapy Resistance for Acute Myeloid Leukemia with Adverse Genetic Factors.

Daisuke Ikeda, SungGi Chi, Satoshi Uchiyama, Hirotaka Nakamura, Yong-Mei Guo, Nobuhiko Yamauchi, Junichiro Yuda, Yosuke Minami

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.7field-weighted citation impact, top 6% 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

18 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
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  10. Regulation of HOX gene expression in AML.Blood cancer journal · 2024
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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

8 authors at 2 institutions in 1 country.

Daisuke IkedaDepartment of Hematology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.ORCID 0000-0002-7398-4616
SungGi ChiDepartment of Hematology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.ORCID 0000-0002-5725-7187
Satoshi UchiyamaDepartment of Hematology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.
Hirotaka NakamuraDepartment of Hematology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.
Yong-Mei GuoDepartment of Hematology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.
Nobuhiko YamauchiDepartment of Hematology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.
Junichiro YudaDepartment of Hematology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.
Yosuke MinamiDepartment of Hematology, National Cancer Center Hospital East, Kashiwa, Chiba 277-8577, Japan.
National Cancer Center Hospital East · JPKameda Medical Center · JP

Funding

National Cancer Research and Development expenses grant 2021-A-11
6 · The paper itself

Abstract

The European LeukemiaNet (ELN) criteria define the adverse genetic factors of acute myeloid leukemia (AML). AML with adverse genetic factors uniformly shows resistance to standard chemotherapy and is associated with poor prognosis. Here, we focus on the biological background and real-world etiology of these adverse genetic factors and then describe a strategy to overcome the clinical disadvantages in terms of targeting pivotal molecular mechanisms. Different adverse genetic factors often rely on common pathways.

Indexed as

Leukemia, Myeloid, AcuteProto-Oncogene Proteins c-aktChromosomal Proteins, Non-Histonefms-Like Tyrosine Kinase 3Fusion Proteins, bcr-ablHumansMutationNucleophosminOncogene ProteinsPoly-ADP-Ribose Binding ProteinsChromosomal Proteins, Non-HistoneDEK protein, humanfms-Like Tyrosine Kinase 3Fusion Proteins, bcr-ablNucleophosminOncogene ProteinsPoly-ADP-Ribose Binding ProteinsProto-Oncogene Proteins c-aktAMLanti-CD47 antibodyASXL1 mutationBCR-ABL1 fusioncomplex karyotypeDEK-NUP214 fusionELN classificationFLT3-ITD with wild-type NPM1haploinsufficiency of GATA2 and mis-expression of MECOMKMT2A rearrangementmeninRUNX1 mutationTP53 mutation

Identifiers

PMID35682627
PMCPMC9180585
OpenAlexW4281558793

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.