Evidence map›Paper›PMID 31817878›Full record

ReviewInternational journal of molecular sciences2019

Circulating Extracellular Vesicles Containing Xenobiotic Metabolizing CYP Enzymes and Their Potential Roles in Extrahepatic Cells Via Cell-Cell Interactions.

Kelli Gerth, Sunitha Kodidela, Madeline Mahon, Sanjana Haque, Neha Verma, Santosh Kumar

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
1.8field-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

24 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Designing cytochrome P450 enzymes for use in cancer gene therapy.Frontiers in bioengineering and biotechnology · 2024
    Review
  8. Role of Extracellular Vesicles in Liver Diseases.Life (Basel, Switzerland) · 2023
    Review
  9. Article
  10. Article
  11. Review
  12. The Role of Extracellular Vesicles in Liver Pathogenesis.The American journal of pathology · 2022
    Review
  13. Review
  14. Review
  15. Microvesicles: the functional mediators in sorafenib resistance.Cancer drug resistance (Alhambra, Calif.) · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
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

6 authors at 1 institution in 1 country.

Kelli GerthDepartment of Pharmaceutical sciences, University of Tennessee Health Science Center, 881 Madison Avenue, Memphis, TN 38163, USA.
Sunitha KodidelaDepartment of Pharmaceutical sciences, University of Tennessee Health Science Center, 881 Madison Avenue, Memphis, TN 38163, USA.ORCID 0000-0002-9385-5985
Madeline MahonDepartment of Pharmaceutical sciences, University of Tennessee Health Science Center, 881 Madison Avenue, Memphis, TN 38163, USA.
Sanjana HaqueDepartment of Pharmaceutical sciences, University of Tennessee Health Science Center, 881 Madison Avenue, Memphis, TN 38163, USA.
Neha VermaDepartment of Pharmaceutical sciences, University of Tennessee Health Science Center, 881 Madison Avenue, Memphis, TN 38163, USA.
Santosh KumarDepartment of Pharmaceutical sciences, University of Tennessee Health Science Center, 881 Madison Avenue, Memphis, TN 38163, USA.
University of Tennessee Health Science Center · US

Funding

NIH HHS DA047178
6 · The paper itself

Abstract

The cytochrome P450 (CYP) family of enzymes is known to metabolize the majority of xenobiotics. Hepatocytes, powerhouses of CYP enzymes, are where most drugs are metabolized into non-toxic metabolites. Additional tissues/cells such as gut, kidneys, lungs, blood, and brain cells express selective CYP enzymes. Extrahepatic CYP enzymes, especially in kidneys, also metabolize drugs into excretable forms. However, extrahepatic cells express a much lower level of CYPs than hepatocytes. It is possible that the liver secretes CYP enzymes, which circulate via plasma and are eventually delivered to extrahepatic cells (e.g., brain cells). CYP circulation likely occurs via extracellular vesicles (EVs), which carry important biomolecules for delivery to distant cells. Recent studies have revealed an abundance of several CYPs in plasma EVs and other cell-derived EVs, and have demonstrated the role of CYP-containing EVs in xenobiotic-induced toxicity via cell-cell interactions. Thus, it is important to study the mechanism for packaging CYP into EVs, their circulation via plasma, and their role in extrahepatic cells. Future studies could help to find novel EV biomarkers and help to utilize EVs in novel interventions via CYP-containing EV drug delivery. This review mainly covers the abundance of CYPs in plasma EVs and EVs derived from CYP-expressing cells, as well as the potential role of EV CYPs in cell-cell communication and their application with respect to novel biomarkers and therapeutic interventions.

Indexed as

Cell CommunicationAnimalsCytochrome P-450 Enzyme SystemExtracellular VesiclesHumansInactivation, MetabolicLiverXenobioticsCytochrome P-450 Enzyme SystemXenobioticscirculatory CYPscytochrome P450exosomesextracellular vesiclesextrahepatic tissuesplasma

Identifiers

PMID31817878
PMCPMC6940889
OpenAlexW2992985923

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.