Evidence map›Paper›PMID 36568260›Full record

ArticleCurrent research in pharmacology and drug discovery2022

Structural analysis of cannabinoids against EGFR-TK leads a novel target against EGFR-driven cell lines.

Thomanai Lamtha, Lueacha Tabtimmai, Napat Songtawee, Natthasit Tansakul, Kiattawee Choowongkomon

Open access · goldAbstract read
In one paragraph

Article in Current research in pharmacology and drug discovery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
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  5. Identification of MAPK3 inhibitors againstJournal of veterinary science · 2025
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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

5 authors at 4 institutions in 1 country.

Thomanai LamthaLaboratory of Protein Engineering and Bioinformatics (PROTEB), Department of Biochemistry, Faculty of Science, Kasetsart University, Bangkok, 10900, Thailand.
Lueacha TabtimmaiDepartment of Biotechnology, Faculty of Applied Science, King Mongkut's University of Technology North Bangkok, Bangkok, 10800, Thailand.
Napat SongtaweeDepartment of Clinical Chemistry, Faculty of Medical Technology, Mahidol University, Nakhon Pathom, 73170, Thailand.
Natthasit TansakulDepartment of Pharmacology, Faculty of Veterinary Medicine, Kasetsart University, Bangkok, 10900, Thailand.
Kiattawee ChoowongkomonLaboratory of Protein Engineering and Bioinformatics (PROTEB), Department of Biochemistry, Faculty of Science, Kasetsart University, Bangkok, 10900, Thailand.
Kasetsart University · THKing Mongkut's University of Technology North Bangkok · THMahidol University · THNational Science and Technology Development Agency · TH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epidermal growth factor receptor (EGFR) is a member of the ErbB family of proteins and are involved in downstream signal transduction, plays prominent roles in cell growth regulation, proliferation, and the differentiation of many cell types. They are correlated with the stage and severity of cancer. Therefore, EGFRs are targeted proteins for the design of new drugs to treat cancers that overexpress these proteins. Currently, several bioactive natural extracts are being studied for therapeutic purposes. Cannabis has been reported in many studies to have beneficial medicinal effects, such as anti-inflammatory, analgesic, antibacterial, and anti-inflammatory effects, and antitumor activity. However, it is unclear whether cannabinoids reduce intracellular signaling by inhibiting tyrosine kinase phosphorylation. In this study, cannabinoids (CBD, CBG, and CBN) were simulated for binding to the EGFR-intracellular domain to evaluate the binding energy and binding mode based on molecular docking simulation. The results showed that the binding site was almost always located at the kinase active site. In addition, the compounds were tested for binding affinity and demonstrated their ability to inhibit kinase enzymes. Furthermore, the compounds potently inhibited cellular survival and apoptosis induction in either of the EGFR-overexpressing cell lines.

Indexed as

CBDCBD, CannabidiolCBGCBG, CannabigerolCBNCBN, CannabinolEGFREGFR-TK, Epidermal growth factor receptor-tyrosine kinaseMolecular dynamics simulationsSPR, Surface plasmon resonanceTyrosine-kinase inhibition

Identifiers

PMID36568260
PMCPMC9780064
OpenAlexW4298127550

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.