Evidence map›Paper›PMID 32152231›Full record

ArticleThe Journal of biological chemistry2020

AIG1 and ADTRP are endogenous hydrolases of fatty acid esters of hydroxy fatty acids (FAHFAs) in mice.

Meric Erikci Ertunc, Bernard P Kok, William H Parsons, Justin G Wang, Dan Tan, Cynthia J Donaldson, Antonio F M Pinto, Joan M Vaughan, Nhi Ngo, Kenneth M Lum and 6 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.8field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Distinct roles of adipose triglyceride lipase and hormone-sensitive lipase in the catabolism of triacylglycerol estolides.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  20. Article
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 2 countries.

Meric Erikci ErtuncClayton Foundation Laboratories for Peptide Biology, The Salk Institute for Biological Studies, La Jolla, California 92037.
Bernard P KokDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, California 92037.
William H ParsonsDepartment of Chemistry and Biochemistry, Oberlin College, Oberlin, Ohio 44074.
Justin G WangClayton Foundation Laboratories for Peptide Biology, The Salk Institute for Biological Studies, La Jolla, California 92037.
Dan TanClayton Foundation Laboratories for Peptide Biology, The Salk Institute for Biological Studies, La Jolla, California 92037.
Cynthia J DonaldsonClayton Foundation Laboratories for Peptide Biology, The Salk Institute for Biological Studies, La Jolla, California 92037.
Antonio F M PintoClayton Foundation Laboratories for Peptide Biology, The Salk Institute for Biological Studies, La Jolla, California 92037.
Joan M VaughanClayton Foundation Laboratories for Peptide Biology, The Salk Institute for Biological Studies, La Jolla, California 92037.
Nhi NgoLundbeck La Jolla Research Center, Inc., San Diego, California 92121.
Kenneth M LumLundbeck La Jolla Research Center, Inc., San Diego, California 92121.
Cassandra L HenryLundbeck La Jolla Research Center, Inc., San Diego, California 92121.
Aundrea R CoppolaLundbeck La Jolla Research Center, Inc., San Diego, California 92121.
Micah J NiphakisLundbeck La Jolla Research Center, Inc., San Diego, California 92121.
Benjamin F CravattDepartment of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, La Jolla, California 92037.
Enrique SaezDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, California 92037.
Alan SaghatelianClayton Foundation Laboratories for Peptide Biology, The Salk Institute for Biological Studies, La Jolla, California 92037. Electronic address: asaghatelian@salk.edu.
Salk Institute for Biological Studies · USLa Jolla Alcohol Research · USScripps Research Institute · USOberlin College · US

Funding

Viral Vector Core (VVC)P30CA014195 · NCI · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI Ye Zheng · 1985 to 2026
$82.8M
Chemoproteomic Identification and Therapeutic Validation of Proteins of Metabolic SignificanceRC2DK114785 · NIDDK · SCRIPPS RESEARCH INSTITUTE, THE · PI CRAVATT, BENJAMIN F, SAEZ, ENRIQUE · 2017 to 2021
$8.2M
Regulation of the biosynthesis of a novel class of anti-diabetic lipidsR01DK106210 · NIDDK · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KAHN, BARBARA B., SAGHATELIAN, ALAN · 2016 to 2024
$6.6M
CHEMOPROTEOMIC METHODS FOR SERINE HYDROLASE INHIBITOR DEVELOPMENTR01DA033760 · NIDA · SCRIPPS RESEARCH INSTITUTE, THE · PI CRAVATT, BENJAMIN F, SCAMPAVIA, LOUIS DANIEL · 2012 to 2021
$5.1M
Integrated Acoustic Transfer System for HTS Library ManagementS10OD025279 · OD · SCRIPPS FLORIDA · PI SCAMPAVIA, LOUIS DANIEL · 2018 to 2018
$624k
A Hybrid Quadrupole-Orbitrap LC/MSS10OD021815 · OD · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI SAGHATELIAN, ALAN · 2016 to 2016
$580k
HTS Drug  Discovery DispensersS10OD026857 · OD · SCRIPPS FLORIDA · PI SCAMPAVIA, LOUIS DANIEL · 2019 to 2019
$452k
Role of Novel Branched Chain Fatty Acids in Amelioration of Metabolic DiseaseF32DK111159 · NIDDK · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI ERIKCI ERTUNC, MERIC · 2017 to 2019
$184k
NCI NIH HHS P30 CA014195NIDA NIH HHS R01 DA033760NIDDK NIH HHS F32 DK111159NIDDK NIH HHS R01 DK106210NIDDK NIH HHS RC2 DK114785NIH HHS S10 OD021815NIH HHS S10 OD025279NIH HHS S10 OD026857
6 · The paper itself

Abstract

Fatty acid esters of hydroxy fatty acids (FAHFAs) are a newly discovered class of signaling lipids with anti-inflammatory and anti-diabetic properties. However, the endogenous regulation of FAHFAs remains a pressing but unanswered question. Here, using MS-based FAHFA hydrolysis assays, LC-MS-based lipidomics analyses, and activity-based protein profiling, we found that androgen-induced gene 1 (AIG1) and androgen-dependent TFPI-regulating protein (ADTRP), two threonine hydrolases, control FAHFA levels

Indexed as

AnimalsEsterasesEstersFatty AcidsGene Knockout TechniquesHydrolysisMembrane ProteinsMiceAdtrp protein, mouseAIG1 protein, mouseEsterasesEstersFatty AcidsMembrane Proteinsandrogen-dependent TFPI-regulating protein (ADTRP)androgen induced gene 1 (AIG1)diabetesenzyme inhibitorfatty acid ester of hydroxy fatty acid (FAHFA)glucose metabolismlipid esterlipid signalingmetabolismthreonine hydrolase

Identifiers

PMID32152231
PMCPMC7196635
OpenAlexW3010577680

What OpenQuestion holds

Textmetadata
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.