Evidence map›Paper›PMID 34879239›Full record

ArticleCell metabolism2021

NEAT1 is essential for metabolic changes that promote breast cancer growth and metastasis.

Mi Kyung Park, Li Zhang, Kyung-Won Min, Jung-Hyun Cho, Chih-Chen Yeh, Hyesu Moon, Daniel Hormaechea-Agulla, Hyejin Mun, Seungbeom Ko, Ji Won Lee and 15 more

Open access · greenAbstract read
In one paragraph

Article in Cell metabolism, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 138 papers.

0numbers the graph read from it
0cells of the map it votes in
138citing papers in PubMed
12.2field-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

138 citing papers in PubMed, 202 citations in OpenAlex.

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  18. Glycolysis enzymes and cellular lactylation in tumour.Clinical and translational medicine · 2026
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78 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

25 authors at 7 institutions in 3 countries.

Mi Kyung ParkDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Li ZhangDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Kyung-Won MinDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425, USA; Department of Biology, College of Natural Sciences, Gangneung-Wonju National University, Gangneung-si, Gangwon-do 25457, Republic of Korea.
Jung-Hyun ChoDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425, USA.
Chih-Chen YehDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Hyesu MoonSoonchunhyang Institute of Medi-bio Science, Soonchunhyang University, Cheonan-si, Chungcheongnam-do 31151, Republic of Korea.
Daniel Hormaechea-AgullaDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Hyejin MunDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425, USA.
Seungbeom KoDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425, USA.
Ji Won LeeDepartment of Biology, College of Natural Sciences, Gangneung-Wonju National University, Gangneung-si, Gangwon-do 25457, Republic of Korea.
Sonali JatharDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425, USA; Laboratory of lncRNA Biology, National Center for Cell Science, Pune, Maharashtra 411007, India.
Aubrey S SmithDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425, USA.
Yixin YaoDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Nguyen Thu GiangDepartment of Biology Education, Kyungpook National University, Daegu 41566, Republic of Korea.
Hong Ha VuDepartment of Biology Education, Kyungpook National University, Daegu 41566, Republic of Korea.
Victoria C YanDepartment of Cancer Systems Imaging, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Mary C BridgesDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC 29425, USA.
Antonis KourtidisDepartment of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC 29425, USA.
Florian MullerDepartment of Cancer Systems Imaging, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Jeong Ho ChangDepartment of Biology Education, Kyungpook National University, Daegu 41566, Republic of Korea.
Su Jung SongSoonchunhyang Institute of Medi-bio Science, Soonchunhyang University, Cheonan-si, Chungcheongnam-do 31151, Republic of Korea.
Shinichi NakagawaFaculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Hokkaido 060-0812, Japan.
Tetsuro HiroseGraduate School of Frontier Biosciences, Osaka University, Suita, Osaka 565-0871, Japan.
Je-Hyun YoonDepartment of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC 29425, USA. Electronic address: yoonje@musc.edu.
Min Sup SongDepartment of Molecular and Cellular Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA. Electronic address: msong1@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USMedical University of South Carolina · USKyungpook National University · KRSoonchunhyang University · KRGangneung–Wonju National University · KRHokkaido University · JPOsaka University · JP

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND N. DUBOIS · 2009 to 2026
$42.7M
South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
The role of SMAD1 and SATB2 in colon patterningP20GM130457 · NIGMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI STEPHEN A DUNCAN · 2020 to 2026
$18.7M
Proteomics CoreP30DK123704 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI DON C. ROCKEY · 2020 to 2026
$8.8M
South Carolina Clinical & Translational Research Institute (SCTR)TL1TR001451 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI FEGHALI-BOSTWICK, CAROL A. · 2015 to 2024
$4.6M
The role of PTEN feedback mechanism in cancerR01CA196740 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Min Sup Song · 2016 to 2026
$3.4M
Targeting m6A RNA epigenetics in treatment-emergent neuroendocrine prostate cancerR01CA258100 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SONG, MIN SUP · 2021 to 2025
$1.8M
Epithelial adherens junctions regulate colon cell behavior through RNAi and lncRNAsR01DK124553 · NIDDK · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI KOURTIDIS, ANTONIS · 2021 to 2024
$1.3M
PIWI - Transposon regulation by epithelial adherens junctionsR21CA246233 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI KOURTIDIS, ANTONIS · 2020 to 2021
$384k
NCATS NIH HHS TL1 TR001451NCATS NIH HHS UL1 TR001450NCI NIH HHS P30 CA016672NCI NIH HHS P30 CA138313NCI NIH HHS R01 CA196740NCI NIH HHS R01 CA258100NCI NIH HHS R21 CA246233NIDDK NIH HHS P30 DK123704NIDDK NIH HHS R01 DK124553NIGMS NIH HHS P20 GM130457
6 · The paper itself

Abstract

Accelerated glycolysis is the main metabolic change observed in cancer, but the underlying molecular mechanisms and their role in cancer progression remain poorly understood. Here, we show that the deletion of the long noncoding RNA (lncRNA) Neat1 in MMTV-PyVT mice profoundly impairs tumor initiation, growth, and metastasis, specifically switching off the penultimate step of glycolysis. Mechanistically, NEAT1 directly binds and forms a scaffold bridge for the assembly of PGK1/PGAM1/ENO1 complexes and thereby promotes substrate channeling for high and efficient glycolysis. Notably, NEAT1 is upregulated in cancer patients and correlates with high levels of these complexes, and genetic and pharmacological blockade of penultimate glycolysis ablates NEAT1-dependent tumorigenesis. Finally, we demonstrate that Pinin mediates glucose-stimulated nuclear export of NEAT1, through which it exerts isoform-specific and paraspeckle-independent functions. These findings establish a direct role for NEAT1 in regulating tumor metabolism, provide new insights into the Warburg effect, and identify potential targets for therapy.

Indexed as

Breast NeoplasmsMicroRNAsRNA, Long NoncodingAnimalsCell Line, TumorCell ProliferationFemaleGene Expression Regulation, NeoplasticGlycolysisHumansMiceMicroRNAsNEAT1 long non-coding RNA, humanNEAT1 long non-coding RNA, mouseRNA, Long Noncodingaerobic glycolysisbreast cancerENO1long noncoding RNANEAT1PGAM1PGK1Pinintumor metabolismWarburg effect

Identifiers

PMID34879239
PMCPMC8813003
OpenAlexW4200441227

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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.