Evidence map›Paper›PMID 30930145›Full record

ArticleCell stem cell2019

The Mitochondrial Transacylase, Tafazzin, Regulates for AML Stemness by Modulating Intracellular Levels of Phospholipids.

Ayesh K Seneviratne, Mingjing Xu, Juan J Aristizabal Henao, Val A Fajardo, Zhenyue Hao, Veronique Voisin, G Wei Xu, Rose Hurren, S Kim, Neil MacLean and 26 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Cell stem cell, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

39 citing papers in PubMed, 56 citations in OpenAlex.

  1. Review
  2. Article
  3. International journal of molecular sciences · 2026
    Article
  4. Article
  5. Cardiolipin preserves TNature metabolism · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Regulating Lipid MetabolismRecent patents on anti-cancer drug discovery · 2025
    Article
  13. Metabolic dependencies of acute myeloid leukemia stem cells.International journal of hematology · 2024
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. The critical role of cardiolipin in metazoan differentiation, development, and maturation.Developmental dynamics : an official publication of the American Association of Anatomists · 2023
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

36 authors at 10 institutions in 5 countries.

Ayesh K SeneviratnePrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada; Institute of Medical Sciences, Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Mingjing XuPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Juan J Aristizabal HenaoLaboratory of Nutritional Lipidomics, Department of Kinesiology, University of Waterloo, Waterloo, ON, Canada.
Val A FajardoDepartment of Health Sciences, Faculty of Applied Health Sciences, Brock University, St. Catharines, ON, Canada.
Zhenyue HaoPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Veronique VoisinDepartment of Molecular Genetics, University of Toronto, Toronto, ON, Canada.
G Wei XuPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Rose HurrenPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
S KimPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Neil MacLeanPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Xiaoming WangPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Marcela GrondaPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Danny JeyarajuPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Yulia JitkovaPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Troy KetelaPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Michael MullokandovDepartment of Biological Regulation, Weizmann Institute, Rehovot, Israel.
David SharonPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Geethu ThomasPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Raphaël Chouinard-WatkinsDepartment of Nutritional Sciences, Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
James R HawleyPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada; Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
Caitlin SchaferDepartment of Pediatrics, College of Medicine, University of Cincinnati, Cincinnati, OH, USA.
Helen Loo YauPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada; Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
Zaza KhuchuaDepartment of Biochemistry, Sechenov Medical University, Moscow, Russian Federation; Institute of Medical Research Ilia State University, Tbilisi, Georgia.
Ahmed AmanDrug Discovery Program, Ontario Institute for Cancer Research, Toronto, ON, Canada; Department of Pharmacology and Toxicology, University of Toronto, ON, Canada.
Rima Al-AwarDrug Discovery Program, Ontario Institute for Cancer Research, Toronto, ON, Canada; Department of Pharmacology and Toxicology, University of Toronto, ON, Canada.
Atan GrossDepartment of Biological Regulation, Weizmann Institute, Rehovot, Israel.
Steven M ClaypoolDepartment of Physiology, School of Medicine, Johns Hopkins University, Baltimore, MD, USA.
Richard P BazinetDepartment of Nutritional Sciences, Faculty of Medicine, University of Toronto, Toronto, ON, Canada.
Mathieu LupienPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada; Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
Steven ChanPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada; Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
Daniel D De CarvalhoPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada; Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
Mark D MindenPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada; Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada.
Gary D BaderDepartment of Molecular Genetics, University of Toronto, Toronto, ON, Canada.
Ken D StarkLaboratory of Nutritional Lipidomics, Department of Kinesiology, University of Waterloo, Waterloo, ON, Canada.
Paul LeBlancDepartment of Health Sciences, Faculty of Applied Health Sciences, Brock University, St. Catharines, ON, Canada.
Aaron D SchimmerPrincess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada; Institute of Medical Sciences, Faculty of Medicine, University of Toronto, Toronto, ON, Canada; Department of Medical Biophysics, University of Toronto, Toronto, ON, Canada. Electronic address: aaron.schimmer@uhn.ca.
Princess Margaret Cancer Centre · CAUniversity of Toronto · CAUniversity Health Network · CABrock University · CAUniversity of Waterloo · CAWeizmann Institute of Science · ILIlia State University · GEJohns Hopkins Medicine · USOntario Institute for Cancer Research · CAUniversity of Cincinnati Medical Center · US

Funding

Cytoscape: A Modeling Platform for Biomolecular NetworksR01HG009979 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI IDEKER, TREY · 2017 to 2021
$3.5M
Mitochondrial phosphatidylethanolamine metabolismR01GM111548 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI CLAYPOOL, STEVEN MICHAEL · 2014 to 2021
$2.8M
Cardiolipin and the mitochondrial ADP/ATP carrier interactomeR01HL108882 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI CLAYPOOL, STEVEN MICHAEL · 2013 to 2017
$2.0M
CIHRNHGRI NIH HHS R01 HG009979NHLBI NIH HHS R01 HL108882NIGMS NIH HHS R01 GM111548
6 · The paper itself

Abstract

Tafazzin (TAZ) is a mitochondrial transacylase that remodels the mitochondrial cardiolipin into its mature form. Through a CRISPR screen, we identified TAZ as necessary for the growth and viability of acute myeloid leukemia (AML) cells. Genetic inhibition of TAZ reduced stemness and increased differentiation of AML cells both in vitro and in vivo. In contrast, knockdown of TAZ did not impair normal hematopoiesis under basal conditions. Mechanistically, inhibition of TAZ decreased levels of cardiolipin but also altered global levels of intracellular phospholipids, including phosphatidylserine, which controlled AML stemness and differentiation by modulating toll-like receptor (TLR) signaling.

Indexed as

AcyltransferasesAnimalsCell Line, TumorDoxorubicinFemaleHumansLeukemia, Myeloid, AcuteMaleMiceMice, Inbred NODMice, SCIDMice, TransgenicMitochondriaPhospholipidsSignal TransductionToll-Like ReceptorsAcyltransferasesDoxorubicinPhospholipidsTAFAZZIN protein, humanToll-Like ReceptorsTranscription Factorsacute myeloid leukemiacancer differentiationcardiolipinleukemia initiating cellmitochondriaphosphatidylserinephospholipidstafazzin

Identifiers

PMID30930145
PMCPMC7137093
OpenAlexW2926366685

What OpenQuestion holds

Textmetadata
LicenceTDM
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.