Evidence map›Paper›PMID 29317755›Full record

ArticleScientific reports2018

In vitro and in vivo antitumor potential of carvacrol nanoemulsion against human lung adenocarcinoma A549 cells via mitochondrial mediated apoptosis.

Imran Khan, Ashutosh Bahuguna, Pradeep Kumar, Vivek K Bajpai, Sun Chul Kang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 2 pooled it
18.1field-weighted citation impact, top 1% 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

45 citing papers in PubMed, 2 syntheses or guidelines pooled it, 155 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
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  5. Review
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  7. Review
  8. Article
  9. Article
  10. Plant Based Extract Oil-Based Nano emulsions: Impact on Human Melanoma Cell Line.Asian Pacific journal of cancer prevention : APJCP · 2024
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  11. Review
  12. Antiviral Effects of Secondary Metabolites fromPlants (Basel, Switzerland) · 2023
    Article
  13. Review
  14. Antimicrobial, Antibiofilm, and Anticancer Activities ofMolecules (Basel, Switzerland) · 2023
    Article
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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 3 institutions in 2 countries.

Imran KhanDepartment of Biotechnology, Daegu University, Gyeongsan, Gyeongbuk, 712-714, Republic of Korea.
Ashutosh BahugunaDepartment of Biotechnology, Daegu University, Gyeongsan, Gyeongbuk, 712-714, Republic of Korea.
Pradeep KumarDepartment of Forestry, North Eastern Regional Institute of Science and Technology, Nirjuli, India. pkbiotech@gmail.com.ORCID http://orcid.org/0000-0002-0892-5425
Vivek K BajpaiDepartment of Energy and Materials Engineering, Dongguk University-Seoul, Seoul, Republic of Korea. vbajpai04@yahoo.com.
Sun Chul KangDepartment of Biotechnology, Daegu University, Gyeongsan, Gyeongbuk, 712-714, Republic of Korea. sckang@daegu.ac.kr.
Daegu University · KRDongguk University · KRNorth Eastern Regional Institute of Science and Technology · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Carvacrol is present abundantly in the essential oils of many medicinal plants and well known for its numerous biological activities. Since partial solubility in water and physicochemical instability limits its industrial uses, the present study was performed to prepare a carvacrol nanoemulsion (CANE) using an ultrasonication technique and further evaluation of its anticancer potential against human lung adenocarcinoma A549 cells. The nanoemulsion formulation was optimized by varying carvacrol and polysorbate 80 ratios and characterized by dynamic light scattering (DLS), which revealed a negative surface charge with a mean droplet size between 105.5 ± 3.4 to 169.8 ± 4.9 nm. The CANE induced reactive oxygen species (ROS) production in A549 cells, leading to activation of key regulators of apoptosis such as p-JNK, Bax and Bcl2 as well as release of cytochrome C, and activation of the caspase cascade. Suppression of mitochondrial ROS using Mito-TEMPO reversed the apoptotic potential of CANE signifying involvement of mitochondrial ROS in cell death. Beside, CANE displayed a strong antitumor potential in vivo using an athymic nude mice model. The results strongly support that CANE induced apoptosis in A549 cells by induction of ROS and could be a promising candidate for lung cancer therapy.

Indexed as

EmulsionsA549 CellsAdenocarcinomaAdenocarcinoma of LungAnimalsAntineoplastic Agents, PhytogenicApoptosisApoptosis Regulatory ProteinsCell Line, TumorCell SurvivalCymenesGene Expression RegulationHumansLung NeoplasmsMembrane Potential, MitochondrialMiceAntineoplastic Agents, PhytogenicApoptosis Regulatory ProteinscarvacrolCymenesEmulsionsMonoterpenesReactive Oxygen Species

Identifiers

PMID29317755
PMCPMC5760660
OpenAlexW2781711310

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.