Evidence map›Paper›PMID 34495991›Full record

ArticlePloS one2021

Analysis of electric cigarette liquid effect on mouse brain tumor growth through EGFR and ERK activation.

Hyung Joon Kwon, Young Taek Oh, Saewhan Park, Sung Soo Kim, Jinju Park, Jinlong Yin, Jun Hee Hong, Chan Il Kim, Haseo Ryu, Jong Bae Park and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Toxicity and Appeal of Flavoured E-Cigarettes and Flavour Ban Outcomes: A Narrative Review.International journal of environmental research and public health · 2026
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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

11 authors at 2 institutions in 1 country.

Hyung Joon KwonDepartment of Cancer Control and Population Health, National Cancer Center Graduate School of Cancer Science and Policy, Goyang, South Korea.
Young Taek OhDivision of Clinical Research Institute and Hospital, National Cancer Center, Goyang, Republic of Korea.
Saewhan ParkDepartment of Cancer Biomedical Science, National Cancer Center Graduate School of Cancer Science and Policy, Goyang, South Korea.
Sung Soo KimDepartment of Cancer Biomedical Science, National Cancer Center Graduate School of Cancer Science and Policy, Goyang, South Korea.
Jinju ParkDepartment of Cancer Control and Population Health, National Cancer Center Graduate School of Cancer Science and Policy, Goyang, South Korea.
Jinlong YinDivision of Clinical Research Institute and Hospital, National Cancer Center, Goyang, Republic of Korea.
Jun Hee HongDivision of Clinical Research Institute and Hospital, National Cancer Center, Goyang, Republic of Korea.
Chan Il KimDepartment of Cancer Biomedical Science, National Cancer Center Graduate School of Cancer Science and Policy, Goyang, South Korea.
Haseo RyuDepartment of Cancer Biomedical Science, National Cancer Center Graduate School of Cancer Science and Policy, Goyang, South Korea.
Jong Bae ParkDivision of Clinical Research Institute and Hospital, National Cancer Center, Goyang, Republic of Korea.
Min Kyung LimDepartment of Cancer Control and Population Health, National Cancer Center Graduate School of Cancer Science and Policy, Goyang, South Korea.ORCID 0000-0002-8224-2171
National Cancer Center · KRInha University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionRecently, electric cigarettes with liquid (e-liquid) were introduced as an alternative to tobacco smoking. They were promoted as possible cessation aids and were considered to be potentially less harmful than traditional tobacco-based cigarettes. However, there is little information on the toxicants present in e-liquids and their possible carcinogenic effects.

methodsWestern blot analysis was performed to identify the protein levels of cancer progression related signal transducers. Patient-derived brain tumor cells (CSC2) were injected into mouse brains and tumor growth was then observed by performing magnetic resonance imaging (MRI) and hematoxylin and eosin (H&E) staining of the whole brain. Immunohistochemistry (IHC) staining and Immunofluorescence staining were performed to study the expression of pEGFR and pERK.

resultsWestern blotting revealed that e-liquids increased pEGFR and pERK expression in a dose dependent manner. Animal experiments revealed that the e-liquid treated group had accelerated tumor growth and poor prognosis compared to the vehicle group. Histological staining showed activation of pEGFR and pERK in the e-liquid treated group.

conclusionOur study revealed that e-liquid activates pEGFR and pERK, leading to accelerated brain tumor growth and poor prognosis.

Indexed as

Electronic Nicotine Delivery SystemsAnimalsAstrocytesBrain NeoplasmsCarcinogenesisCell ProliferationCells, CulturedCigarette SmokingDisease Models, AnimalErbB ReceptorsExtracellular Signal-Regulated MAP KinasesFemaleGlioblastomaHeterograftsHumansMAP Kinase Signaling SystemEGFR protein, humanErbB ReceptorsExtracellular Signal-Regulated MAP KinasesNicotinePropylene GlycolSolutionsSolvents

Identifiers

PMID34495991
PMCPMC8425573
OpenAlexW3196644303

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.