Evidence map›Paper›PMID 38750343›Full record

ReviewInternational journal of hematology2024

Metabolic dependencies of acute myeloid leukemia stem cells.

Xiangguo Shi, Mengdie Feng, Daisuke Nakada

Abstract readReview
In one paragraph

Review in International journal of hematology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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

3 authors.

Xiangguo Shi *Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA. xiangguo.shi@bcm.edu.
Mengdie Feng *Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Daisuke Nakada *Department of Molecular & Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA. nakada@bcm.edu.ORCID http://orcid.org/0000-0001-6010-7094

Funding

Project 3: Contribution of inflammation and DNA damaging factors to clonal expansion and malignant transformation in a community cohort of older adultsP01CA265748 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Koichi Takahashi · 2022 to 2026
$13.6M
METABOLIC REGULATION IN LEUKEMIA-INITIATING CELLSR01CA193235 · NCI · BAYLOR COLLEGE OF MEDICINE · PI NAKADA, DAISUKE · 2015 to 2024
$4.6M
THE ROLE OF SELENOPROTEIN SYNTHESIS PATHWAY IN ACUTE MYELOID LEUKEMIAR01CA255813 · NCI · BAYLOR COLLEGE OF MEDICINE · PI NAKADA, DAISUKE · 2021 to 2025
$2.3M
NCI NIH HHS P01 CA265748NCI NIH HHS P01CA265748NCI NIH HHS R01 CA193235NCI NIH HHS R01CA193235NCI NIH HHS R01 CA255813NCI NIH HHS R01CA255813
6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a heterogeneous hematologic malignancy primarily driven by an immature population of AML cells termed leukemia stem cells (LSCs) that are implicated in AML development, chemoresistance, and relapse. An emerging area of research in AML focuses on identifying and targeting the aberrant metabolism in LSCs. Dysregulated metabolism is involved in sustaining functional properties of LSCs, impeding myeloid differentiation, and evading programmed cell death, both in the process of leukemogenesis and in response to chemotherapy. This review discusses recent discoveries regarding the aberrant metabolic processes of AML LSCs that have begun to change the therapeutic landscape of AML.

Indexed as

Leukemia, Myeloid, AcuteNeoplastic Stem CellsAnimalsCell DifferentiationDrug Resistance, NeoplasmHumansAcute myeloid leukemiaLeukemia stem cellMetabolic regulation

Identifiers

PMID38750343
PMCPMC11779507

What OpenQuestion holds

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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.