Evidence map›Paper›PMID 37642045›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2023

In Silico Prediction of Selected Bioactive Compounds Present in Alpinia elegans (C.Presl) K.Schum Seed Oil as Potential Drug Candidates Against Human Cancer Cell Lines.

Jane Marie N Caasi, Raiza Isabel D G Baldoza, Mary Sophia C Bauzon, Mirabella Anne F Odtohan, Librado A Santiago, Myla R Santiago-Bautista

Open access · goldAbstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

6 authors at 1 institution in 1 country.

Jane Marie N CaasiDepartment of Biochemistry, Faculty of Pharmacy, University of Santo Tomas, Manila, Philippines.
Raiza Isabel D G BaldozaDepartment of Biochemistry, Faculty of Pharmacy, University of Santo Tomas, Manila, Philippines.
Mary Sophia C BauzonDepartment of Biochemistry, Faculty of Pharmacy, University of Santo Tomas, Manila, Philippines.
Mirabella Anne F OdtohanDepartment of Biochemistry, Faculty of Pharmacy, University of Santo Tomas, Manila, Philippines.
Librado A SantiagoDepartment of Biochemistry, Faculty of Pharmacy, University of Santo Tomas, Manila, Philippines.ORCID 0000-0003-3188-0699
Myla R Santiago-BautistaDepartment of Biochemistry, Faculty of Pharmacy, University of Santo Tomas, Manila, Philippines.ORCID 0000-0001-9173-7320
University of Santo Tomas · PH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAlpinia elegans (Zingiberaceae) is a Philippine endemic plant reported to have various folkloric uses. The seed oil of A. elegans has been shown to contain a majority of the following bioactive compounds: D-limonene, α-pinene, and caryophyllene oxide. The study sought to determine if the bioactive compounds found in A. elegans seed oil would be a good natural, inexpensive, and less-detrimental alternative for cancer treatment.

methodsThe study utilized in silico (Way2Drug predictive services, SwissADME, AutoDock 4) experiment to examine the aforementioned compounds as viable therapeutic candidates against human cancer cell lines.

resultResults determined that the compounds D-limonene, α-pinene, and caryophyllene oxide were most potent against thyroid gland carcinoma (8505C) cells, brain glaucoma (Hs 683) cells, and promyeloblast leukemia (HL-60) cells, respectively. Additionally, D-limonene was the only compound to show arrhythmia as an adverse effect. Predictions showed that the compounds could inhibit cellular growth factors and serine/threonine-protein kinase activity. The compounds generated a bioavailability score of 0.55 and exhibited blood-brain barrier (BBB) penetration. D-limonene, α-pinene, and caryophyllene oxide had binding energy of -4.59, -5.43, and -6.92, respectively.

conclusionThe binding energy indicated that the ligands could securely dock to the receptors, thus suggesting that interaction between the ligands and receptors was stable. Results have shown that the compounds are promising candidates against human cancer cell lines by inhibiting cell proliferation and inducing apoptosis.

Indexed as

AlpiniaNeoplasmsBicyclic MonoterpenesHL-60 CellsHumansLigandsLimonenePlant OilsPolycyclic Sesquiterpenesalpha-pineneBicyclic Monoterpenescaryophyllene oxideLigandsLimonenePlant OilsPolycyclic SesquiterpenesApoptosiscancercaryophyllene oxideD-limoneneα -pinene

Identifiers

PMID37642045
PMCPMC10685237
OpenAlexW4386258037

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.