Evidence map›Paper›PMID 35896750›Full record

ArticleNature2022

PI3K drives the de novo synthesis of coenzyme A from vitamin B5.

Christian C Dibble, Samuel A Barritt, Grace E Perry, Evan C Lien, Renee C Geck, Sarah E DuBois-Coyne, David Bartee, Thomas T Zengeya, Emily B Cohen, Min Yuan and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Nature, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
7.5field-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

57 citing papers in PubMed, 93 citations in OpenAlex.

  1. Article
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  4. Metabolic-epigenetic reprogrammingActa pharmaceutica Sinica. B · 2026
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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

16 authors at 4 institutions in 1 country.

Christian C Dibble *Department of Pathology, Cancer Research Institute, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA. ccdibble@bidmc.harvard.edu.ORCID http://orcid.org/0000-0002-1122-9017
Samuel A Barritt *Department of Pathology, Cancer Research Institute, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0002-3241-1272
Grace E PerryDepartment of Pathology, Cancer Research Institute, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0002-0404-9237
Evan C LienDepartment of Pathology, Cancer Research Institute, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Renee C GeckDepartment of Pathology, Cancer Research Institute, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0001-7812-7675
Sarah E DuBois-CoyneDepartment of Pathology, Cancer Research Institute, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
David BarteeChemical Biology Laboratory, National Cancer Institute, Frederick, MD, USA.ORCID http://orcid.org/0000-0001-8090-4242
Thomas T ZengeyaChemical Biology Laboratory, National Cancer Institute, Frederick, MD, USA.
Emily B CohenDepartment of Pathology, Cancer Research Institute, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Min YuanMass Spectrometry Core, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Benjamin D HopkinsDepartment of Genetics and Genomic Sciences, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.ORCID http://orcid.org/0000-0002-7970-6430
Jordan L MeierChemical Biology Laboratory, National Cancer Institute, Frederick, MD, USA.
John G ClohessyPreclinical Murine Pharmacogenetics Facility and Mouse Hospital, Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA, USA.ORCID http://orcid.org/0000-0001-5186-9775
John M AsaraMass Spectrometry Core, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Lewis C CantleyThe Sandra and Edward Meyer Cancer Center, Weill Medical College of Cornell University, New York, NY, USA.ORCID http://orcid.org/0000-0002-1298-7653
Alex TokerDepartment of Pathology, Cancer Research Institute, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA. atoker@bidmc.harvard.edu.ORCID http://orcid.org/0000-0003-0723-4419
Beth Israel Deaconess Medical Center · USNational Cancer Institute · USCornell University · USIcahn School of Medicine at Mount Sinai · US

Funding

VectorP30CA006516 · NCI · DANA-FARBER CANCER INSTITUTE · PI A. Heather Eliassen · 1985 to 2026
$330.6M
Tuberous Sclerosis-Pathway and PathogenesisP01CA120964 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI David J. Kwiatkowski · 2007 to 2026
$35.9M
Targeting Cancer Through Modifications and MetabolismZIABC011488 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI MEIER, JORDAN L · 2013 to 2025
$21.3M
Discovery, Regulation and Function of the PI 3-Kinase and AKT Pathway in CancerR35CA253097 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI Alex Toker · 2020 to 2026
$6.9M
Novel regulation of PI3K/Akt to direct targeted breast cancer therapiesR01CA177910 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI WEI, WENYI · 2013 to 2023
$3.9M
Role of Vitamin B5 and Coenzyme A Metabolism in PI3K Driven TumorigenesisR00CA194314 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI DIBBLE, CHRISTIAN · 2018 to 2020
$747k
Utilizing Precision Medicine to elucidate the mechanisms underpinning treatment efficacyR00CA230384 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI HOPKINS, BENJAMIN D. · 2019 to 2021
$718k
Regulation of arginine metabolism as a therapeutic target in breast cancerF31CA213460 · NCI · HARVARD MEDICAL SCHOOL · PI GECK, RENEE CATHERINE · 2017 to 2019
$107k
Regulation of the cell cycle and growth signaling pathways by a sensing mechanism for Vitamin B5-Coenzyme A metabolismF31CA254169 · NCI · HARVARD MEDICAL SCHOOL · PI BARRITT, SAMUEL · 2020 to 2022
$83k
Intramural NIH HHS ZIA BC011488NCI NIH HHS F31 CA213460NCI NIH HHS F31 CA254169NCI NIH HHS P01 CA120964NCI NIH HHS P30 CA006516NCI NIH HHS R00 CA194314NCI NIH HHS R00 CA230384NCI NIH HHS R01 CA177910NCI NIH HHS R35 CA253097
6 · The paper itself

Abstract

In response to hormones and growth factors, the class I phosphoinositide-3-kinase (PI3K) signalling network functions as a major regulator of metabolism and growth, governing cellular nutrient uptake, energy generation, reducing cofactor production and macromolecule biosynthesis

Indexed as

Coenzyme APantothenic AcidPhosphatidylinositol 3-KinaseAcetyl Coenzyme AAdenosine TriphosphateCell ProliferationCysteineLipid MetabolismMass SpectrometryMetabolomicsPhosphorylationPhosphotransferases (Alcohol Group Acceptor)Proto-Oncogene Proteins c-aktSignal TransductionAcetyl Coenzyme AAdenosine TriphosphateCoenzyme ACysteinepantothenate kinasePantothenic AcidPhosphatidylinositol 3-KinasePhosphotransferases (Alcohol Group Acceptor)Proto-Oncogene Proteins c-akt

Identifiers

PMID35896750
PMCPMC9352595
OpenAlexW4288051653

What OpenQuestion holds

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LicenceCC BY
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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.