Evidence map›Paper›PMID 31993306›Full record

ReviewActa pharmaceutica Sinica. B2020

Cytochrome P450 endoplasmic reticulum-associated degradation (ERAD): therapeutic and pathophysiological implications.

Doyoung Kwon, Sung-Mi Kim, Maria Almira Correia

Open access · diamondAbstract readReview
In one paragraph

Review in Acta pharmaceutica Sinica. B, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

27 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Ubiquitination and Metabolic Disease.Advances in experimental medicine and biology · 2024
    Review
  10. Article
  11. Acta pharmaceutica Sinica. B · 2023
    Article
  12. Review
  13. Review
  14. PGRMC1: An enigmatic heme-binding protein.Pharmacology & therapeutics · 2023
    Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. 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

3 authors at 1 institution in 1 country.

Doyoung KwonDepartment of Cellular and Molecular Pharmacology, University of California San Francisco, San Francisco, CA 94158-2517, USA.
Sung-Mi KimDepartment of Cellular and Molecular Pharmacology, University of California San Francisco, San Francisco, CA 94158-2517, USA.
Maria Almira CorreiaDepartment of Cellular and Molecular Pharmacology, University of California San Francisco, San Francisco, CA 94158-2517, USA.
University of California, San Francisco · US

Funding

UCSF Liver Core CenterP30DK026743 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Jennifer Y. Chen · 1986 to 2026
$30.7M
HEPATIC DEGRADATION OF P450P ISOZYMESR01GM044037 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CORREIA, MARIA ALMIRA · 1990 to 2023
$8.0M
REGULATION OF HEME METABOLISM IN THE LIVERR01DK026506 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CORREIA, MARIA ALMIRA · 1986 to 2016
$7.1M
NIDDK NIH HHS P30 DK026743NIDDK NIH HHS R01 DK026506NIGMS NIH HHS R01 GM044037
6 · The paper itself

Abstract

The hepatic endoplasmic reticulum (ER)-anchored cytochromes P450 (P450s) are mixed-function oxidases engaged in the biotransformation of physiologically relevant endobiotics as well as of myriad xenobiotics of therapeutic and environmental relevance. P450 ER-content and hence function is regulated by their coordinated hemoprotein syntheses and proteolytic turnover. Such P450 proteolytic turnover occurs through a process known as ER-associated degradation (ERAD) that involves ubiquitin-dependent proteasomal degradation (UPD) and/or autophagic-lysosomal degradation (ALD). Herein, on the basis of available literature reports and our own recent findings of

Indexed as

3MA, 3-methyladenineAAA, ATPases associated with various cellular activitiesACC1, acetyl-CoA carboxylase 1ACC2, acetyl-CoA carboxylase 2ACHE, acetylcholinesteraseACOX1, acyl-CoA oxidase 1AdipoR1, gene of adiponectin receptor 1ALD, autophagic-lysosomal degradationAMPK1AP-1, activator protein 1ASK1, apoptosis signal-regulating kinaseATF2, activating transcription factor 2Atg14, autophagy-related 14CBZ, carbamazepineCHIP, carboxy-terminus of Hsc70-interacting proteinCHIP E3 ubiquitin ligaseCytochromes P450Endoplasmic reticulum-associated degradationFas, fatty acid synthaseFOXO, forkhead box OGAPDH, glyceraldehyde 3-phosphate dehydrogenasegp78/AMFR, autocrine motility factor receptorgp78/AMFR E3 ubiquitin ligaseIl-1β, interleukin 1 βIl-6, interleukin 6INH, isoniazidInsig1, insulin-induced gene 1IRS1, insulin receptor substrate 1JNK1Lpl, lipoprotein lipaseMcp1, chemokine (C–C motif) ligand 1Non-alcoholic fatty liver diseaseNon-alcoholic steatohepatitisPgc1, peroxisome proliferator-activated receptor coactivator 1Scd1, stearoyl-coenzyme A desaturaseshRNAi, shRNA interferenceSREBP1c, sterol regulatory element binding transcription factor 1cTnf, tumor necrosis factorUb, ubiquitinUPD, ubiquitin (Ub)-dependent proteasomal degradation

Identifiers

PMID31993306
PMCPMC6976991
OpenAlexW2983797785

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.