Evidence map›Paper›PMID 37192295›Full record

ArticleBlood2023

Metabolic adaptation to tyrosine kinase inhibition in leukemia stem cells.

Shaowei Qiu, Vipul Sheth, Chengcheng Yan, Juan Liu, Balu K Chacko, Hui Li, David K Crossman, Seth D Fortmann, Sajesan Aryal, Ashley Rennhack and 8 more

Open access · greenAbstract read
In one paragraph

Article in Blood, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
9.0field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 31 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 2 institutions in 2 countries.

Shaowei QiuDivision of Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0003-3866-0066
Vipul ShethDivision of Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL.
Chengcheng YanDivision of Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL.
Juan LiuDepartment of Pharmacology and Cancer Biology, Duke University School of Medicine, Durham, NC.
Balu K ChackoDepartment of Pathology, Mitochondrial Medicine Laboratory, University of Alabama at Birmingham, Birmingham, AL.
Hui LiDivision of Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL.
David K CrossmanGenomics Core Facility, University of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0002-0981-169X
Seth D FortmannDepartment of Ophthalmology and Visual Sciences, University of Alabama at Birmingham, Birmingham, AL.
Sajesan AryalDivision of Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0001-6154-0586
Ashley RennhackDivision of Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL.
Maria B GrantDepartment of Ophthalmology and Visual Sciences, University of Alabama at Birmingham, Birmingham, AL.
Robert S WelnerDivision of Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL.
Andrew J PatersonDivision of Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL.
Adam R WendeDepartment of Pathology, Mitochondrial Medicine Laboratory, University of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0002-5536-4675
Victor M Darley-UsmarDepartment of Pathology, Mitochondrial Medicine Laboratory, University of Alabama at Birmingham, Birmingham, AL.
Rui LuDivision of Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0003-1593-2612
Jason W LocasaleDepartment of Pharmacology and Cancer Biology, Duke University School of Medicine, Durham, NC.
Ravi BhatiaDivision of Hematology and Oncology, University of Alabama at Birmingham, Birmingham, AL.ORCID 0000-0001-5740-2316
University of Alabama at Birmingham · USDuke University · US

Funding

XRAY CRYSTALLOGRAPHYP30CA013148 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Robert S Welner · 1985 to 2026
$165.9M
Visual Phenotyping CoreP30EY003039 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Paul Douglas Gamlin · 1985 to 2026
$16.9M
Resistance of CML stem cells to STI571 (Gleevec)R01CA095684 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BHATIA, RAVI · 2003 to 2017
$4.6M
LXR as a Novel Therapeutic Target in Diabetic RetinopathyR01EY025383 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BUSIK, JULIA V, GRANT, MARIA BARTOLOMEO · 2015 to 2024
$4.2M
Microenvironmental Regulation of Leukemia Stem CellsR01CA172447 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BHATIA, RAVI · 2013 to 2023
$3.4M
Leukemia stem cell regulation and resistanceR01CA248794 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BHATIA, RAVI · 2021 to 2025
$2.1M
Role of choroidal macrophages in regulating lipid homeostasis and immunosuppression of the RPE/choroidF30EY033198 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI FORTMANN, SETH D · 2021 to 2024
$180k
NCI NIH HHS P30 CA013148NCI NIH HHS R01 CA095684NCI NIH HHS R01 CA172447NCI NIH HHS R01 CA248794NEI NIH HHS F30 EY033198NEI NIH HHS P30 EY003039NEI NIH HHS R01 EY025383
6 · The paper itself

Abstract

Tyrosine kinase inhibitors (TKIs) are very effective in treating chronic myelogenous leukemia (CML), but primitive, quiescent leukemia stem cells persist as a barrier to the cure. We performed a comprehensive evaluation of metabolic adaptation to TKI treatment and its role in CML hematopoietic stem and progenitor cell persistence. Using a CML mouse model, we found that glycolysis, glutaminolysis, the tricarboxylic acid cycle, and oxidative phosphorylation (OXPHOS) were initially inhibited by TKI treatment in CML-committed progenitors but were restored with continued treatment, reflecting both selection and metabolic reprogramming of specific subpopulations. TKI treatment selectively enriched primitive CML stem cells with reduced metabolic gene expression. Persistent CML stem cells also showed metabolic adaptation to TKI treatment through altered substrate use and mitochondrial respiration maintenance. Evaluation of transcription factors underlying these changes helped detect increased HIF-1 protein levels and activity in TKI-treated stem cells. Treatment with an HIF-1 inhibitor in combination with TKI treatment depleted murine and human CML stem cells. HIF-1 inhibition increased mitochondrial activity and reactive oxygen species (ROS) levels, reduced quiescence, increased cycling, and reduced the self-renewal and regenerating potential of dormant CML stem cells. We, therefore, identified the HIF-1-mediated inhibition of OXPHOS and ROS and maintenance of CML stem cell dormancy and repopulating potential as a key mechanism of CML stem cell adaptation to TKI treatment. Our results identify a key metabolic dependency in CML stem cells persisting after TKI treatment that can be targeted to enhance their elimination.

Indexed as

Leukemia, Myelogenous, Chronic, BCR-ABL PositiveProtein-Tyrosine KinasesAnimalsDrug Resistance, NeoplasmHumansMiceNeoplastic Stem CellsProtein Kinase InhibitorsReactive Oxygen SpeciesProtein Kinase InhibitorsProtein-Tyrosine KinasesReactive Oxygen Species

Identifiers

PMID37192295
PMCPMC10447615
OpenAlexW4376638313

What OpenQuestion holds

Textmetadata
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.