Evidence map›Paper›PMID 39125600›Full record

SynthesisInternational journal of molecular sciences2024

Systematic Review of Naturally Derived Substances That Act as Inhibitors of the Nicotine Metabolizing Enzyme Cytochrome P450 2A6.

Haralampos Tzoupis, Konstantinos D Papavasileiou, Stavros Papatzelos, Angelos Mavrogiorgis, Lefteris C Zacharia, Georgia Melagraki, Antreas Afantitis

Abstract readSystematic Review
In one paragraph

Synthesis in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. 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

7 authors.

Haralampos TzoupisDepartment of ChemInformatics, NovaMechanics Ltd., Nicosia 1070, Cyprus.
Konstantinos D PapavasileiouDepartment of ChemInformatics, NovaMechanics Ltd., Nicosia 1070, Cyprus.ORCID 0000-0002-2322-7422
Stavros PapatzelosDepartment of ChemInformatics, NovaMechanics Ltd., Nicosia 1070, Cyprus.
Angelos MavrogiorgisDepartment of ChemInformatics, NovaMechanics Ltd., Nicosia 1070, Cyprus.
Lefteris C ZachariaSchool of Life and Health Sciences, University of Nicosia, Nicosia 1700, Cyprus.ORCID 0000-0002-0327-2373
Georgia MelagrakiDivision of Physical Sciences and Applications, Hellenic Military Academy, 16672 Vari, Greece.
Antreas AfantitisDepartment of ChemInformatics, NovaMechanics Ltd., Nicosia 1070, Cyprus.ORCID 0000-0002-0977-8180

Funding

Research and Innovation Foundation RNSMOKE ENTERPRISES/0223/Sub-call1/0262
6 · The paper itself

Abstract

Tobacco smoking has been highlighted as a major health challenge in modern societies. Despite not causing death directly, smoking has been associated with several health issues, such as cardiovascular diseases, respiratory disorders, and several cancer types. Moreover, exposure to nicotine during pregnancy has been associated with adverse neurological disorders in babies. Nicotine Replacement Therapy (NRT) is the most common strategy employed for smoking cessation, but despite its widespread use, NRT presents with low success and adherence rates. This is attributed partially to the rate of nicotine metabolism by cytochrome P450 2A6 (CYP2A6) in each individual. Nicotine addiction is correlated with the high rate of its metabolism, and thus, novel strategies need to be implemented in NRT protocols. Naturally derived products are a cost-efficient and rich source for potential inhibitors, with the main advantages being their abundance and ease of isolation. This systematic review aims to summarize the natural products that have been identified as CYP2A6 inhibitors, validated through in vitro and/or in vivo assays, and could be implemented as nicotine metabolism inhibitors. The scope is to present the different compounds and highlight their possible implementation in NRT strategies. Additionally, this information would provide valuable insight regarding CYP2A6 inhibitors, that can be utilized in drug development via the use of in silico methodologies and machine-learning models to identify new potential lead compounds for optimization and implementation in NRT regimes.

Indexed as

Cytochrome P-450 CYP2A6NicotineAnimalsBiological ProductsHumansBiological ProductsCYP2A6 protein, humanCytochrome P-450 CYP2A6NicotineCYP450 inhibitioncytochrome P450natural productsnicotinereplacement therapysmoking cessation

Identifiers

PMID39125600
PMCPMC11312336

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.