Evidence map›Paper›PMID 33672718›Full record

ReviewInternational journal of molecular sciences2021

Molecular Regulation of Canalicular ABC Transporters.

Amel Ben Saad, Alix Bruneau, Elodie Mareux, Martine Lapalus, Jean-Louis Delaunay, Emmanuel Gonzales, Emmanuel Jacquemin, Tounsia Aït-Slimane, Thomas Falguières

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Molecular Basis of Bile Acid-FXR-FGF15/19 Signaling Axis.International journal of molecular sciences · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. RAB10 Interacts with ABCB4 and Regulates Its Intracellular Traffic.International journal of molecular sciences · 2021
    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

9 authors at 1 institution in 2 countries.

Amel Ben SaadPhysiopathogénèse et Traitement des Maladies du foie, Inserm, Université Paris-Saclay, UMR_S 1193, Hepatinov, 91400 Orsay, France.ORCID 0000-0003-2105-1491
Alix BruneauCentre de Recherche Saint-Antoine (CRSA), Inserm, Sorbonne Université, UMR_S 938, Institute of Cardiometabolism and Nutrition (ICAN), 75012 Paris, France.ORCID 0000-0002-5740-2372
Elodie MareuxPhysiopathogénèse et Traitement des Maladies du foie, Inserm, Université Paris-Saclay, UMR_S 1193, Hepatinov, 91400 Orsay, France.ORCID 0000-0002-0474-9217
Martine LapalusPhysiopathogénèse et Traitement des Maladies du foie, Inserm, Université Paris-Saclay, UMR_S 1193, Hepatinov, 91400 Orsay, France.ORCID 0000-0002-7033-831X
Jean-Louis DelaunayCentre de Recherche Saint-Antoine (CRSA), Inserm, Sorbonne Université, UMR_S 938, Institute of Cardiometabolism and Nutrition (ICAN), 75012 Paris, France.
Emmanuel GonzalesPhysiopathogénèse et Traitement des Maladies du foie, Inserm, Université Paris-Saclay, UMR_S 1193, Hepatinov, 91400 Orsay, France.ORCID 0000-0002-1546-3193
Emmanuel JacqueminPhysiopathogénèse et Traitement des Maladies du foie, Inserm, Université Paris-Saclay, UMR_S 1193, Hepatinov, 91400 Orsay, France.
Tounsia Aït-SlimaneCentre de Recherche Saint-Antoine (CRSA), Inserm, Sorbonne Université, UMR_S 938, Institute of Cardiometabolism and Nutrition (ICAN), 75012 Paris, France.
Thomas FalguièresPhysiopathogénèse et Traitement des Maladies du foie, Inserm, Université Paris-Saclay, UMR_S 1193, Hepatinov, 91400 Orsay, France.ORCID 0000-0003-2867-0500
Inserm · FR

Funding

Agence Nationale de la Recherche ANR-15-CE14-0008-01Association Française pour l'Etude du Foie XXXAssociation Mucoviscidose-ABCF2 XXXFondation pour la Recherche Médicale FRM-EQU-2020-03010517German Research Foundation 403224013Ministère de l'Enseignement supérieur, de la Recherche et de l'Innovation XXX
6 · The paper itself

Abstract

The ATP-binding cassette (ABC) transporters expressed at the canalicular membrane of hepatocytes mediate the secretion of several compounds into the bile canaliculi and therefore play a key role in bile secretion. Among these transporters, ABCB11 secretes bile acids, ABCB4 translocates phosphatidylcholine and ABCG5/G8 is responsible for cholesterol secretion, while ABCB1 and ABCC2 transport a variety of drugs and other compounds. The dysfunction of these transporters leads to severe, rare, evolutionary biliary diseases. The development of new therapies for patients with these diseases requires a deep understanding of the biology of these transporters. In this review, we report the current knowledge regarding the regulation of canalicular ABC transporters' folding, trafficking, membrane stability and function, and we highlight the role of molecular partners in these regulating mechanisms.

Indexed as

AnimalsATP-Binding Cassette TransportersBile CanaliculiEndocytosisGlycosylationHepatocytesHumansMultidrug Resistance-Associated Protein 2UbiquitinationABCC2 protein, humanATP-Binding Cassette TransportersMultidrug Resistance-Associated Protein 2ABCB1ABCB11ABCB4ABCC2ABCG5/G8bile secretionmolecular partners

Identifiers

PMID33672718
PMCPMC7924332
OpenAlexW3132003040

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.