Evidence map›Paper›PMID 30270124›Full record

ArticleCancer cell2018

Subversion of Systemic Glucose Metabolism as a Mechanism to Support the Growth of Leukemia Cells.

Haobin Ye, Biniam Adane, Nabilah Khan, Erica Alexeev, Nichole Nusbacher, Mohammad Minhajuddin, Brett M Stevens, Amanda C Winters, Xi Lin, John M Ashton and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
5.2field-weighted citation impact, top 3% 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

77 citing papers in PubMed, 111 citations in OpenAlex.

  1. Insulin-like growth factor receptor signaling in physiology and disease.Signal transduction and targeted therapy · 2026
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  12. Metabolic dependencies of acute myeloid leukemia stem cells.International journal of hematology · 2024
    Review
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17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 3 institutions in 1 country.

Haobin YeDivision of Hematology, University of Colorado Anschutz Medical Campus, 12700 E 19(th) Avenue, Aurora, CO 80045, USA.
Biniam AdaneDivision of Hematology, University of Colorado Anschutz Medical Campus, 12700 E 19(th) Avenue, Aurora, CO 80045, USA.
Nabilah KhanDivision of Hematology, University of Colorado Anschutz Medical Campus, 12700 E 19(th) Avenue, Aurora, CO 80045, USA.
Erica AlexeevMucosal Inflammation Program, University of Colorado Anschutz Medical Campus, 12700 E 19(th) Avenue, Aurora, CO 80045, USA.
Nichole NusbacherDivision of Biomedical Informatics and Personalized Medicine, Department of Medicine, University of Colorado Anschutz Medical Campus, 12700 E 19(th) Avenue, Aurora, CO 80045, USA.
Mohammad MinhajuddinDivision of Hematology, University of Colorado Anschutz Medical Campus, 12700 E 19(th) Avenue, Aurora, CO 80045, USA.
Brett M StevensDivision of Hematology, University of Colorado Anschutz Medical Campus, 12700 E 19(th) Avenue, Aurora, CO 80045, USA.
Amanda C WintersCenter for Cancer and Blood Disorders, Children's Hospital Colorado, 13123 E 16th Avenue, Aurora, CO 80045, USA.
Xi LinDepartment of Pathology and Laboratory Medicine, University of Rochester, 601 Elmwood Avenue, Rochester, NY 14642, USA.
John M AshtonFunctional Genomics Center, University of Rochester, 601 Elmwood Avenue, Rochester, NY 14642, USA.
Enkhtsetseg PurevDivision of Hematology, University of Colorado Anschutz Medical Campus, 12700 E 19(th) Avenue, Aurora, CO 80045, USA.
Lianping XingDepartment of Pathology and Laboratory Medicine, University of Rochester, 601 Elmwood Avenue, Rochester, NY 14642, USA.
Daniel A PollyeaDivision of Hematology, University of Colorado Anschutz Medical Campus, 12700 E 19(th) Avenue, Aurora, CO 80045, USA.
Catherine A LozuponeDivision of Biomedical Informatics and Personalized Medicine, Department of Medicine, University of Colorado Anschutz Medical Campus, 12700 E 19(th) Avenue, Aurora, CO 80045, USA.
Natalie J SerkovaDepartment of Radiology, Animal Imaging Shared Resources, University of Colorado Anschutz Medical Campus, 12700 E 19(th) Avenue, Aurora, CO 80045, USA.
Sean P ColganMucosal Inflammation Program, University of Colorado Anschutz Medical Campus, 12700 E 19(th) Avenue, Aurora, CO 80045, USA.
Craig T JordanDivision of Hematology, University of Colorado Anschutz Medical Campus, 12700 E 19(th) Avenue, Aurora, CO 80045, USA. Electronic address: craig.jordan@ucdenver.edu.
University of Colorado Anschutz Medical Campus · USUniversity of Rochester · USChildren's Hospital Colorado · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Wendy M Kohrt · 1995 to 2026
$32.6M
Metabolic Regulation of Inflammation by Microbial SCFAR01DK104713 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Sean P Colgan · 2015 to 2026
$4.7M
Hypoxia, HIF, and Mucosal InflammationR37DK050189 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI COLGAN, SEAN P · 2010 to 2019
$4.1M
Bruker 9.4T/ 20cm BioSpec MR Scanner for Colorado Animal Imaging Shared ResourcesS10OD023485 · OD · UNIVERSITY OF COLORADO DENVER · PI SERKOVA, NATALIE J. · 2017 to 2017
$2.0M
ONCOGENE COOPERATIVITY IN LEUKEMIA STEM CELLSR01CA166265 · NCI · UNIVERSITY OF ROCHESTER · PI JORDAN, CRAIG T. · 2012 to 2016
$1.7M
Microenvironment-induced metabolic plasticity in leukemia stem cellsR01CA220986 · NCI · UNIVERSITY OF COLORADO DENVER · PI JORDAN, CRAIG T. · 2018 to 2020
$1.1M
Investigating the potential role of NADPH oxidase 2 in regulating the biology of leukemic stem cellsF31CA196330 · NCI · UNIVERSITY OF COLORADO DENVER · PI ADANE, BINIAM · 2015 to 2017
$59k
NCI NIH HHS F31 CA196330NCI NIH HHS P30 CA046934NCI NIH HHS R01 CA166265NCI NIH HHS R01 CA220986NIDDK NIH HHS R01 DK104713NIDDK NIH HHS R37 DK050189NIH HHS S10 OD023485
6 · The paper itself

Abstract

From an organismal perspective, cancer cell populations can be considered analogous to parasites that compete with the host for essential systemic resources such as glucose. Here, we employed leukemia models and human leukemia samples to document a form of adaptive homeostasis, where malignant cells alter systemic physiology through impairment of both host insulin sensitivity and insulin secretion to provide tumors with increased glucose. Mechanistically, tumor cells induce high-level production of IGFBP1 from adipose tissue to mediate insulin sensitivity. Further, leukemia-induced gut dysbiosis, serotonin loss, and incretin inactivation combine to suppress insulin secretion. Importantly, attenuated disease progression and prolonged survival are achieved through disruption of the leukemia-induced adaptive homeostasis. Our studies provide a paradigm for systemic management of leukemic disease.

Indexed as

AnimalsDiet, High-FatGlucoseHomeostasisHumansInsulinInsulin ResistanceLeukemiaMiceGlucoseInsulinadaptive homeostasisadipose tissueIGFBP1insulin resistanceleukemiamicrobiotaserotoninshort-chain fatty acids

Identifiers

PMID30270124
PMCPMC6177322
OpenAlexW2892430625

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.