Evidence map›Paper›PMID 29058718›Full record

ArticleNature cell biology2017

PKM2 methylation by CARM1 activates aerobic glycolysis to promote tumorigenesis.

Fabao Liu, Fengfei Ma, Yuyuan Wang, Ling Hao, Hao Zeng, Chenxi Jia, Yidan Wang, Peng Liu, Irene M Ong, Baobin Li and 5 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Nature cell biology, 2017. 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 177 papers.

0numbers the graph read from it
0cells of the map it votes in
177citing papers in PubMed
9.4field-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

177 citing papers in PubMed, 310 citations in OpenAlex.

  1. Article
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  9. Article
  10. Article
  11. Article
  12. Promising Role of PKM2 in the Diagnosis and Prognosis of Ovarian Cancer.Anti-cancer agents in medicinal chemistry · 2026
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
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117 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 1 institution in 2 countries.

Fabao LiuMcArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, Wisconsin 53705, USA.
Fengfei MaSchool of Pharmacy, University of Wisconsin-Madison, Madison, Wisconsin 53705, USA.
Yuyuan WangDepartment of Materials Science and Engineering and Wisconsin Institute for Discovery, University of Wisconsin-Madison, Madison, Wisconsin 53715, USA.
Ling HaoSchool of Pharmacy, University of Wisconsin-Madison, Madison, Wisconsin 53705, USA.ORCID http://orcid.org/0000-0002-0106-5266
Hao ZengMcArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, Wisconsin 53705, USA.ORCID http://orcid.org/0000-0003-4967-9555
Chenxi JiaSchool of Pharmacy, University of Wisconsin-Madison, Madison, Wisconsin 53705, USA.
Yidan WangMcArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, Wisconsin 53705, USA.
Peng LiuDepartment of Biostatistics and Medical Informatics, University of Wisconsin-Madison, Madison, Wisconsin 53705, USA.
Irene M OngDepartment of Biostatistics and Medical Informatics, University of Wisconsin-Madison, Madison, Wisconsin 53705, USA.
Baobin LiSchool of Pharmacy, University of Wisconsin-Madison, Madison, Wisconsin 53705, USA.
Guojun ChenDepartment of Materials Science and Engineering and Wisconsin Institute for Discovery, University of Wisconsin-Madison, Madison, Wisconsin 53715, USA.
Jiaoyang JiangSchool of Pharmacy, University of Wisconsin-Madison, Madison, Wisconsin 53705, USA.
Shaoqin GongDepartment of Materials Science and Engineering and Wisconsin Institute for Discovery, University of Wisconsin-Madison, Madison, Wisconsin 53715, USA.ORCID http://orcid.org/0000-0001-9447-2938
Lingjun LiSchool of Pharmacy, University of Wisconsin-Madison, Madison, Wisconsin 53705, USA.ORCID http://orcid.org/0000-0003-0056-3869
Wei XuMcArdle Laboratory for Cancer Research, University of Wisconsin-Madison, Madison, Wisconsin 53705, USA.ORCID http://orcid.org/0000-0003-3808-0045
University of Wisconsin–Madison · US

Funding

UW COMPREHENSIVE CANCER CENTER SUPPORTP30CA014520 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI AMY TRENTHAM-DIETZ · 1985 to 2026
$142.6M
TR&D 2 Metabolic Labels for Ultraplexed Protein Quantification p. 453P41GM108538 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI COON, JOSHUA J · 2016 to 2025
$13.1M
Role of Beta-Catenin in Urinary DysfunctionU54DK104310 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI RICKE, WILLIAM A · 2014 to 2023
$12.8M
Mass Spectrometric Studies of Neuropeptides in FeedingR01DK071801 · NIDDK · UNIVERSITY OF WISCONSIN-MADISON · PI LINGJUN LI · 2006 to 2026
$6.7M
Acquisition of a High-Field Dual Source FTICR-MS for Pharmaceutical ResearchS10RR029531 · NCRR · UNIVERSITY OF WISCONSIN-MADISON · PI LI, LINGJUN · 2011 to 2011
$2.1M
Structure, Function and Regulation of Human O-GlcNAcaseR01GM126300 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI JIANG, JIAOYANG · 2017 to 2020
$1.2M
Protein Arginine Methylation in Chemotherapy ResistanceR01CA213293 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI XU, WEI · 2017 to 2021
$795k
Targeting Triple Negative Breast Cancer Using Nanoparticles Loaded with the Anti-Cancer Drug AminoflavoneR21CA196653 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI GONG, SHAOQIN -, XU, WEI · 2016 to 2017
$337k
Seahorse XF96e Metabolic Analyzer purchaseS10OD018039 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI ALEXANDER, CAROLINE M, XU, WEI · 2014 to 2014
$160k
NCI NIH HHS P30 CA014520NCI NIH HHS R01 CA213293NCI NIH HHS R21 CA196653NCRR NIH HHS S10 RR029531NIDDK NIH HHS R01 DK071801NIDDK NIH HHS U54 DK104310NIGMS NIH HHS P41 GM108538NIGMS NIH HHS R01 GM126300NIH HHS S10 OD018039
6 · The paper itself

Abstract

Metabolic reprogramming is a hallmark of cancer. Herein we discover that the key glycolytic enzyme pyruvate kinase M2 isoform (PKM2), but not the related isoform PKM1, is methylated by co-activator-associated arginine methyltransferase 1 (CARM1). PKM2 methylation reversibly shifts the balance of metabolism from oxidative phosphorylation to aerobic glycolysis in breast cancer cells. Oxidative phosphorylation depends on mitochondrial calcium concentration, which becomes critical for cancer cell survival when PKM2 methylation is blocked. By interacting with and suppressing the expression of inositol-1,4,5-trisphosphate receptors (InsP

Indexed as

AnimalsCalciumCarcinogenesisCARD Signaling Adaptor ProteinsCarrier ProteinsCell LineCell Line, TumorCell MovementCell ProliferationEndoplasmic ReticulumFemaleGlycolysisGuanylate CyclaseHEK293 CellsHumansInositol 1,4,5-Trisphosphate ReceptorsCalciumCARD11 protein, humanCARD Signaling Adaptor ProteinsCarrier ProteinsGuanylate CyclaseInositol 1,4,5-Trisphosphate ReceptorsMembrane ProteinsThyroid Hormone-Binding ProteinsThyroid Hormones

Identifiers

PMID29058718
PMCPMC5683091
OpenAlexW2766710101

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.