Evidence map›Paper›PMID 24120138›Full record

ArticleCell2013

PKM2 isoform-specific deletion reveals a differential requirement for pyruvate kinase in tumor cells.

William J Israelsen, Talya L Dayton, Shawn M Davidson, Brian P Fiske, Aaron M Hosios, Gary Bellinger, Jie Li, Yimin Yu, Mika Sasaki, James W Horner and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 333 papers.

0numbers the graph read from it
0cells of the map it votes in
333citing papers in PubMed
15.0field-weighted citation impact, top 1% 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

333 citing papers in PubMed, 544 citations in OpenAlex.

  1. Article
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  11. F13A1-Mediated Macrophage Activation Promotes MASH Progression via the PKM2/HIF1A Pathway.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  12. The moonlighting functions of glycolytic enzymes in tumorigenesis.Cellular oncology (Dordrecht, Netherlands) · 2026
    Review
  13. Review
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review

273 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

22 authors at 9 institutions in 1 country.

William J IsraelsenKoch Institute for Integrative Cancer Research at Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Talya L Dayton
Shawn M Davidson
Brian P Fiske
Aaron M Hosios
Gary Bellinger
Jie Li
Yimin Yu
Mika Sasaki
James W Horner
Laura N Burga
Jianxin Xie
Michael J Jurczak
Ronald A DePinho
Clary B Clish
Tyler Jacks
Richard G Kibbey
Gerburg M Wulf
Dolores Di Vizio
Gordon B Mills
Lewis C Cantley
Matthew G Vander Heiden
Massachusetts Institute of Technology · USBeth Israel Deaconess Medical Center · USDana-Farber Cancer Institute · USThe University of Texas MD Anderson Cancer Center · USYale University · USBroad Institute · USCedars-Sinai Medical Center · USCell Signaling Technology (United States) · USHarvard University · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI MATTHEW G. VANDER HEIDEN · 1985 to 2026
$93.9M
The RAS and P13K Pathways in Pancreatic AdenocarcinomaP01CA117969 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DEPINHO, RONALD ANTHONY · 2006 to 2025
$41.7M
Targeting the PI3K Signaling Pathway in Endometrial CarcinomaP50CA098258 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YUAN, YING · 2003 to 2020
$32.0M
Yale Mouse Metabolic Phenotyping CenterU24DK059635 · NIDDK · YALE UNIVERSITY · PI SHULMAN, GERALD I · 2001 to 2015
$8.9M
PROTEIN KINASE SIGNALING PATHWAYSR01GM056203 · NIGMS · BETH ISRAEL DEACONESS MEDICAL CENTER · PI CANTLEY, LEWIS C. · 1997 to 2012
$4.5M
Regulation of glucose metabolism to allow tumor initiation and growthR01CA168653 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI VANDER HEIDEN, MATTHEW G. · 2013 to 2019
$1.9M
The role of the mitochondrial GTP cycle in insulin secretionR01DK092606 · NIDDK · YALE UNIVERSITY · PI KIBBEY, RICHARD G · 2011 to 2015
$1.8M
Koch Institute Faculty Recruitment for an MD/PHD Physician-ScientistP30CA147882 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI JACKS, TYLER E. · 2009 to 2010
$1.5M
Fatty Acid Synthase, Caveolin-1 and Membrane Microdomains in Prostate CancerR00CA131472 · NCI · CEDARS-SINAI MEDICAL CENTER · PI DI VIZIO, DOLORES · 2010 to 2012
$722k
Yale Mouse Metabolic Phenotyping CenterU2CDK059635 · NIDDK · YALE UNIVERSITY · PI SHULMAN, GERALD I · 2016 to 2016
$493k
Mouse Models to Evaluate the Role of Pyruvate Kinase Regulation in Cancer BiologyK08CA136983 · NCI · DANA-FARBER CANCER INST · PI VANDER HEIDEN, MATTHEW G. · 2008 to 2009
$279k
NCI NIH HHS 5K08CA136983NCI NIH HHS 5P01CA117969NCI NIH HHS 5P30CA14051NCI NIH HHS K08 CA136983NCI NIH HHS P01 CA117969NCI NIH HHS P30 CA014051NCI NIH HHS P30 CA147882NCI NIH HHS P30CA147882NCI NIH HHS P50 CA098258NCI NIH HHS R00 CA131472NCI NIH HHS R00CA131472NCI NIH HHS R01 CA168653NCI NIH HHS R01CA168653NIDDK NIH HHS DK059635NIDDK NIH HHS R01 DK092606NIDDK NIH HHS R01DK092606NIDDK NIH HHS U24 DK059635NIGMS NIH HHS R01 GM056203NIGMS NIH HHS R01GM056203
6 · The paper itself

Abstract

The pyruvate kinase M2 isoform (PKM2) is expressed in cancer and plays a role in regulating anabolic metabolism. To determine whether PKM2 is required for tumor formation or growth, we generated mice with a conditional allele that abolishes PKM2 expression without disrupting PKM1 expression. PKM2 deletion accelerated mammary tumor formation in a Brca1-loss-driven model of breast cancer. PKM2 null tumors displayed heterogeneous PKM1 expression, with PKM1 found in nonproliferating tumor cells and no detectable pyruvate kinase expression in proliferating cells. This suggests that PKM2 is not necessary for tumor cell proliferation and implies that the inactive state of PKM2 is associated with the proliferating cell population within tumors, whereas nonproliferating tumor cells require active pyruvate kinase. Consistent with these findings, variable PKM2 expression and heterozygous PKM2 mutations are found in human tumors. These data suggest that regulation of PKM2 activity supports the different metabolic requirements of proliferating and nonproliferating tumor cells.

Indexed as

Gene DeletionAnimalsBase SequenceBreast NeoplasmsExonsFemaleGene Knockout TechniquesHeterograftsHumansIsoenzymesMammary Neoplasms, ExperimentalMiceMice, Inbred C57BLModels, MolecularMolecular Sequence DataMutagenesisIsoenzymesPyruvate Kinase

Identifiers

PMID24120138
PMCPMC3850755
OpenAlexW1975215468

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.