Evidence map›Paper›PMID 29153836›Full record

ArticleCell2017

Post-transcriptional Regulation of De Novo Lipogenesis by mTORC1-S6K1-SRPK2 Signaling.

Gina Lee, Yuxiang Zheng, Sungyun Cho, Cholsoon Jang, Christina England, Jamie M Dempsey, Yonghao Yu, Xiaolei Liu, Long He, Paola M Cavaliere and 10 more

Abstract read
In one paragraph

Article in Cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 149 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
149citing papers in PubMed, 2 pooled it
6.9field-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

149 citing papers in PubMed, 2 syntheses or guidelines pooled it, 209 citations in OpenAlex.

  1. Oncogenic Role of SRPK2 in Different Types of Cancer: A Systematic Review.Journal of cellular and molecular medicine · 2026
    Pooled it
  2. Alternative splicing and cancer: a systematic review.Signal transduction and targeted therapy · 2021
    Pooled it
  3. Article
  4. Article
  5. Review
  6. Review
  7. An siRNA targetingMolecular therapy. Nucleic acids · 2026
    Article
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  20. Review

89 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

20 authors at 7 institutions in 1 country.

Gina LeeMeyer Cancer Center, Weill Cornell Medicine, New York, NY 10065, USA; Department of Pharmacology, Weill Cornell Medicine, New York, NY 10065, USA.
Yuxiang ZhengMeyer Cancer Center, Weill Cornell Medicine, New York, NY 10065, USA; Department of Medicine, Weill Cornell Medicine, New York, NY 10065, USA.
Sungyun ChoMeyer Cancer Center, Weill Cornell Medicine, New York, NY 10065, USA.
Cholsoon JangLewis-Sigler Institute for Integrative Genomics and Department of Chemistry, Princeton University, Princeton, NJ 08544, USA.
Christina EnglandMeyer Cancer Center, Weill Cornell Medicine, New York, NY 10065, USA.
Jamie M DempseyDepartment of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Yonghao YuDepartment of Biochemistry, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Xiaolei LiuDepartment of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA.
Long HeMeyer Cancer Center, Weill Cornell Medicine, New York, NY 10065, USA; Department of Pharmacology, Weill Cornell Medicine, New York, NY 10065, USA.
Paola M CavaliereMeyer Cancer Center, Weill Cornell Medicine, New York, NY 10065, USA.
Andre ChavezMeyer Cancer Center, Weill Cornell Medicine, New York, NY 10065, USA.
Erik ZhangDepartment of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA.
Meltem IsikJoslin Diabetes Center and Department of Genetics, Harvard Medical School, Boston, MA 02215, USA.
Anthony CouvillonCell Signaling Technology, Danvers, MA 01923, USA.
Noah E DephoureMeyer Cancer Center, Weill Cornell Medicine, New York, NY 10065, USA.
T Keith BlackwellJoslin Diabetes Center and Department of Genetics, Harvard Medical School, Boston, MA 02215, USA.
Jane J YuDepartment of Internal Medicine, University of Cincinnati College of Medicine, Cincinnati, OH 45267, USA.
Joshua D RabinowitzLewis-Sigler Institute for Integrative Genomics and Department of Chemistry, Princeton University, Princeton, NJ 08544, USA.
Lewis C CantleyMeyer Cancer Center, Weill Cornell Medicine, New York, NY 10065, USA; Department of Medicine, Weill Cornell Medicine, New York, NY 10065, USA.
John BlenisMeyer Cancer Center, Weill Cornell Medicine, New York, NY 10065, USA; Department of Pharmacology, Weill Cornell Medicine, New York, NY 10065, USA. Electronic address: job2064@med.cornell.edu.
Cornell University · USWeill Cornell Medicine · USHarvard University · USUniversity of Cincinnati Medical Center · USPrinceton University · USCell Signaling Technology (United States) · USThe University of Texas Southwestern Medical Center · US

Funding

Yale Pathology Tissue Services Shared ResourceP30CA016359 · NCI · YALE UNIVERSITY · PI DAVID L RIMM · 1985 to 2026
$85.0M
SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI JEAN E. SCHAFFER · 1986 to 2026
$50.5M
Tuberous Sclerosis-Pathway and PathogenesisP01CA120964 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI David J. Kwiatkowski · 2007 to 2026
$35.9M
SIGNAL TRANSDUCTION TO PP70 S6KR01GM051405 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI BLENIS, JOHN · 1995 to 2023
$14.0M
ONCOGENIC REGULATION OF S6 PROTEIN KINASE &CELL GROWTHR01CA046595 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI JOHN BLENIS · 1988 to 2026
$10.6M
Role of Phosphoinositides and Protein Kinases in the control of Cancer MetabolismR35CA197588 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI LEWIS C. CANTLEY · 2016 to 2026
$10.2M
Tumor cell metabolism in actionR01CA163591 · NCI · RUTGERS, THE STATE UNIV OF N.J. · PI JOSHUA D RABINOWITZ, Eileen P. White · 2012 to 2026
$7.0M
SKN-1 Regulation and Oxidative Stress Resistance in C. elegansR01GM062891 · NIGMS · JOSLIN DIABETES CENTER · PI BLACKWELL, T KEITH · 2001 to 2016
$5.6M
Signaling mechanisms that detect stress and maintain homeostasis - Research Supplement to Promote Diversity in Health-Related ResearchR35GM122610 · NIGMS · JOSLIN DIABETES CENTER · PI KAHN, C RONALD · 2017 to 2025
$4.7M
The Role of PI3K in Growth RegulationR01GM041890 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI CANTLEY, LEWIS C. · 1990 to 2016
$4.1M
Uncovering Conserved Lipid Homeostasis Mechanisms that Mediate Longevity after Germ Cell Loss in C. ElegansR01AG054215 · NIA · JOSLIN DIABETES CENTER · PI JEAN E. SCHAFFER · 2017 to 2026
$3.9M
Targeting the Estrogen Pathway for the Prevention and Treatment of LAMR01HL098216 · NHLBI · UNIVERSITY OF CINCINNATI · PI YU, JANE · 2010 to 2014
$2.1M
NCI NIH HHS P01 CA120964NCI NIH HHS P30 CA016359NCI NIH HHS R01 CA046595NCI NIH HHS R01 CA163591NCI NIH HHS R35 CA197588NHLBI NIH HHS R01 HL098216NHLBI NIH HHS R01 HL121266NHLBI NIH HHS R01 HL138481NIA NIH HHS R01 AG054215NIDDK NIH HHS P30 DK036836NIDDK NIH HHS R01 DK098331NIGMS NIH HHS R01 GM041890NIGMS NIH HHS R01 GM051405NIGMS NIH HHS R01 GM062891NIGMS NIH HHS R01 GM114160NIGMS NIH HHS R35 GM122610
6 · The paper itself

Abstract

mTORC1 is a signal integrator and master regulator of cellular anabolic processes linked to cell growth and survival. Here, we demonstrate that mTORC1 promotes lipid biogenesis via SRPK2, a key regulator of RNA-binding SR proteins. mTORC1-activated S6K1 phosphorylates SRPK2 at Ser494, which primes Ser497 phosphorylation by CK1. These phosphorylation events promote SRPK2 nuclear translocation and phosphorylation of SR proteins. Genome-wide transcriptome analysis reveals that lipid biosynthetic enzymes are among the downstream targets of mTORC1-SRPK2 signaling. Mechanistically, SRPK2 promotes SR protein binding to U1-70K to induce splicing of lipogenic pre-mRNAs. Inhibition of this signaling pathway leads to intron retention of lipogenic genes, which triggers nonsense-mediated mRNA decay. Genetic or pharmacological inhibition of SRPK2 blunts de novo lipid synthesis, thereby suppressing cell growth. These results thus reveal a novel role of mTORC1-SRPK2 signaling in post-transcriptional regulation of lipid metabolism and demonstrate that SRPK2 is a potential therapeutic target for mTORC1-driven metabolic disorders.

Indexed as

Gene Expression RegulationLipogenesisRNA Processing, Post-TranscriptionalSignal TransductionAnimalsCell NucleusCholesterolFatty AcidsFemaleHeterograftsHumansMechanistic Target of Rapamycin Complex 1MiceMice, NudeNeoplasm TransplantationProtein Serine-Threonine KinasesCholesterolFatty AcidsMechanistic Target of Rapamycin Complex 1Protein Serine-Threonine Kinasesribosomal protein S6 kinase, 70kD, polypeptide 1Ribosomal Protein S6 Kinases, 70-kDaSRPK2 protein, humancancer metabolismCK1de novo lipid synthesismTORnonsense-mediated decayRNA splicingRNA stabilityS6K1SRPK2SR proteins

Identifiers

PMID29153836
PMCPMC5920692
OpenAlexW2770225202

What OpenQuestion holds

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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.