Evidence map›Paper›PMID 38706437›Full record

ReviewExpert opinion on drug metabolism & toxicology2024

Regulation of carboxylesterases and its impact on pharmacokinetics and pharmacodynamics: an up-to-date review.

Yaping Liu, Jiapeng Li, Hao-Jie Zhu

Abstract readReview
In one paragraph

Review in Expert opinion on drug metabolism & toxicology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
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

17 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Biological sex differences in pharmacokinetics and adverse drug reactions.Naunyn-Schmiedeberg's archives of pharmacology · 2026
    Review
  6. Review
  7. Review
  8. Article
  9. Increased Plasma Concentrations of 6-oxo-Methylphenidate inMedicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. 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.

Yaping LiuDepartment of Clinical Pharmacy, University of Michigan, Ann Arbor, MI, USA.
Jiapeng LiDepartment of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, CA, USA.
Hao-Jie ZhuDepartment of Clinical Pharmacy, University of Michigan, Ann Arbor, MI, USA.

Funding

Carboxylesterase 1 Plasma Biomarker for Precision PharmacotherapyR01GM144401 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHU, HAOJIE · 2022 to 2024
$936k
NIGMS NIH HHS R01 GM144401
6 · The paper itself

Abstract

introductionCarboxylesterase 1 (CES1) and carboxylesterase 2 (CES2) are among the most abundant hydrolases in humans, catalyzing the metabolism of numerous clinically important medications, such as methylphenidate and clopidogrel. The large interindividual variability in the expression and activity of CES1 and CES2 affects the pharmacokinetics (PK) and pharmacodynamics (PD) of substrate drugs. AREAS COVERED: This review provides an up-to-date overview of CES expression and activity regulations and examines their impact on the PK and PD of CES substrate drugs. The literature search was conducted on PubMed from inception to January 2024. EXPERT OPINION: Current research revealed modest associations of CES genetic polymorphisms with drug exposure and response. Beyond genomic polymorphisms, transcriptional and posttranslational regulations can also significantly affect CES expression and activity and consequently alter PK and PD. Recent advances in plasma biomarkers of drug-metabolizing enzymes encourage the research of plasma protein and metabolite biomarkers for CES1 and CES2, which could lead to the establishment of precision pharmacotherapy regimens for drugs metabolized by CESs. Moreover, our understanding of tissue-specific expression and substrate selectivity of CES1 and CES2 has shed light on improving the design of CES1- and CES2-activated prodrugs.

Indexed as

Carboxylic Ester HydrolasesAnimalsBiomarkersCarboxylesteraseHumansPharmaceutical PreparationsPolymorphism, GeneticProdrugsBiomarkersCarboxylesteraseCarboxylic Ester HydrolasesCES1 protein, humanCES2 protein, humanPharmaceutical PreparationsProdrugsCarboxylesteraseCES1CES2drug metabolismenvironmental regulatorsgenetic polymorphismspharmacodynamicspharmacokinetics

Identifiers

PMID38706437
PMCPMC11151177

What OpenQuestion holds

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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.