Evidence map›Paper›PMID 28108519›Full record

ArticleCancer research2017

Bone Marrow Adipocytes Facilitate Fatty Acid Oxidation Activating AMPK and a Transcriptional Network Supporting Survival of Acute Monocytic Leukemia Cells.

Yoko Tabe, Shinichi Yamamoto, Kaori Saitoh, Kazumasa Sekihara, Norikazu Monma, Kazuho Ikeo, Kaoru Mogushi, Masato Shikami, Vivian Ruvolo, Jo Ishizawa and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 114 papers.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed
6.2field-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

114 citing papers in PubMed, 167 citations in OpenAlex.

  1. Oxidative Phosphorylation and Fatty Acid Oxidation Are Central to Mitochondrial Metabolism Rewiring in CML Stem/Progenitor Cell Survival.Pathophysiology : the official journal of the International Society for Pathophysiology · 2026
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54 more citing papers are in PubMed but not listed here.

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

21 authors at 6 institutions in 2 countries.

Yoko TabeDepartment of Laboratory Medicine, Juntendo University School of Medicine, Tokyo, Japan.
Shinichi YamamotoDepartment of Laboratory Medicine, Juntendo University School of Medicine, Tokyo, Japan.
Kaori SaitohDepartment of Laboratory Medicine, Juntendo University School of Medicine, Tokyo, Japan.
Kazumasa SekiharaDepartment of Laboratory Medicine, Juntendo University School of Medicine, Tokyo, Japan.
Norikazu MonmaCenter for Information Biology, National Institute of Genetics, Sizuoka, Japan.
Kazuho IkeoCenter for Information Biology, National Institute of Genetics, Sizuoka, Japan.
Kaoru MogushiCenter for Genomic and Regenerative Medicine, Juntendo University School of Medicine, Tokyo, Japan.
Masato ShikamiDepartment of Hematology, Aichi Medical University, Aichi, Japan.
Vivian RuvoloSection of Molecular Hematology and Therapy, Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Jo IshizawaSection of Molecular Hematology and Therapy, Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Numsen HailSection of Molecular Hematology and Therapy, Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Saiko KazunoDivision of Proteomics and BioMolecular Science, Juntendo University School of Medicine, Tokyo, Japan.
Mamoru IgarashiDepartment of Host Defense and Biochemical Research, Juntendo University School of Medicine, Tokyo, Japan.
Hiromichi MatsushitaDepartment of Laboratory Medicine, Tokai University School of Medicine, Kanagawa, Japan.
Yasunari YamanakaPreventive Medicine and Diagnosis Innovation Program, RIKEN, Kanagawa, Japan.
Hajime AraiDivision of Proteomics and BioMolecular Science, Juntendo University School of Medicine, Tokyo, Japan.
Isao NagaokaDepartment of Host Defense and Biochemical Research, Juntendo University School of Medicine, Tokyo, Japan.
Takashi MiidaDepartment of Laboratory Medicine, Juntendo University School of Medicine, Tokyo, Japan.
Yoshihide HayashizakiPreventive Medicine and Diagnosis Innovation Program, RIKEN, Kanagawa, Japan.
Marina KonoplevaSection of Molecular Hematology and Therapy, Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Michael AndreeffSection of Molecular Hematology and Therapy, Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, Texas. mandreef@mdanderson.org.
Juntendo University · JPThe University of Texas MD Anderson Cancer Center · USNational Institute of Genetics · JPRIKEN Center for Integrative Medical Sciences · JPAichi Medical University · JPTokai University · JP

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Leukemia cells in the bone marrow must meet the biochemical demands of increased cell proliferation and also survive by continually adapting to fluctuations in nutrient and oxygen availability. Thus, targeting metabolic abnormalities in leukemia cells located in the bone marrow is a novel therapeutic approach. In this study, we investigated the metabolic role of bone marrow adipocytes in supporting the growth of leukemic blasts. Prevention of nutrient starvation-induced apoptosis of leukemic cells by bone marrow adipocytes, as well as the metabolic and molecular mechanisms involved in this process, was investigated using various analytic techniques. In acute monocytic leukemia (AMoL) cells, the prevention of spontaneous apoptosis by bone marrow adipocytes was associated with an increase in fatty acid β-oxidation (FAO) along with the upregulation of

Indexed as

ApoptosisGene Regulatory NetworksAdipocytesAMP-Activated Protein KinasesBone MarrowCell CycleCell ProliferationCoculture TechniquesFatty AcidsHumansLeukemia, Monocytic, AcuteLipid MetabolismMesenchymal Stem CellsOxidation-Reductionp38 Mitogen-Activated Protein KinasesPhosphorylationAMP-Activated Protein KinasesFatty Acidsp38 Mitogen-Activated Protein KinasesReactive Oxygen Species

Identifiers

PMID28108519
PMCPMC5354955
OpenAlexW2579809204

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.