Evidence map›Paper›PMID 33821592›Full record

ReviewJournal of Korean medical science2021

Recent Clinical Update of Acute Myeloid Leukemia: Focus on Epigenetic Therapies.

Eunyoung Lee, Youngil Koh, Junshik Hong, Hyeon Seok Eom, Sung Soo Yoon

Open access · goldAbstract readReview
In one paragraph

Review in Journal of Korean medical science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Twist1 Promoter Methylation Regulates the Proliferation and Apoptosis of Acute Myeloid Leukemia Cells via PI3K/AKT Pathway.Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion · 2023
    Article
  5. Review
  6. Article
  7. 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 2 institutions in 2 countries.

Eunyoung LeeDepartment of Internal Medicine, Center for Hematologic Malignancy, National Cancer Center, Goyang, Korea.ORCID https://orcid.org/0000-0002-8463-7783
Youngil KohDepartment of Internal Medicine, Seoul National University Hospital, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-8926-8067
Junshik HongDepartment of Internal Medicine, Seoul National University Hospital, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-7829-397X
Hyeon Seok EomDepartment of Internal Medicine, Center for Hematologic Malignancy, National Cancer Center, Goyang, Korea.ORCID https://orcid.org/0000-0002-0484-2067
Sung Soo YoonDepartment of Internal Medicine, Seoul National University Hospital, Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea. ssysmc@snu.ac.kr.ORCID https://orcid.org/0000-0003-2591-7459
Seoul National University Hospital · KRNational Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a complicated disease characterized by genetic heterogeneity and simultaneous alterations in multiple genes. For decades, its only curative method has been intensive induction chemotherapy with or without allogeneic hematopoietic stem cell transplantation, and this approach cannot be applied to elderly patients, who make up more than 50% of AML patients. Recent advances in genomics facilitated the elucidation of various mutations related to AML, and the most frequent mutations were discovered in epigenetic regulators. Alterations to epigenetic modifications that are essential for normal cell biology, including DNA methylation and histone acetylation, have been identified. As epigenetic dysregulation is an important carcinogenic mechanism and some epigenetic changes are reversible, these epigenetic alterations have become targets for novel drug development against AML. This review summarizes the recent advances in epigenetic therapies for AML and discusses future research directions.

Indexed as

EpigenomicsDNA (Cytosine-5-)-MethyltransferasesDrug Therapy, CombinationEnzyme Inhibitorsfms-Like Tyrosine Kinase 3Histone Deacetylase InhibitorsHumansIsocitrate DehydrogenaseLeukemia, Myeloid, AcuteMutationDNA (Cytosine-5-)-MethyltransferasesEnzyme InhibitorsFLT3 protein, humanfms-Like Tyrosine Kinase 3Histone Deacetylase InhibitorsIsocitrate DehydrogenaseAcute Myeloid LeukemiaEpigenetic Therapy

Identifiers

PMID33821592
PMCPMC8021975
OpenAlexW3139053162

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.