Evidence map›Paper›PMID 36012510›Full record

ArticleInternational journal of molecular sciences2022

Protective Effect of Escitalopram on Hepatocellular Carcinoma by Inducing Autophagy.

Li-Jeng Chen, Tsai-Ching Hsu, Hsiang-Lin Chan, Chiao-Fan Lin, Jing-Yu Huang, Robert Stewart, Bor-Show Tzang, Vincent Chin-Hung Chen

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

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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

8 authors at 5 institutions in 2 countries.

Li-Jeng ChenInstitute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan.
Tsai-Ching HsuInstitute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan.
Hsiang-Lin ChanDepartment of Child Psychiatry, Linkou Chang Gung Memorial Hospital, Taoyuan 33305, Taiwan.ORCID 0000-0002-9911-1274
Chiao-Fan LinDepartment of Child Psychiatry, Linkou Chang Gung Memorial Hospital, Taoyuan 33305, Taiwan.
Jing-Yu HuangDepartment of Psychiatry, Chang Gung Medical Foundation, Chiayi Chang Gung Memorial Hospital, Chiayi 61303, Taiwan.
Robert StewartInstitute of Psychiatry, Psychology and Neuroscience, King's College London, London WC2R 2LS, UK.
Bor-Show TzangInstitute of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan.ORCID 0000-0003-0140-9943
Vincent Chin-Hung ChenDepartment of Psychiatry, School of Medicine, Chang Gung University, Taoyuan 33302, Taiwan.
Chang Gung University · TWChung Shan Medical University Hospital · TWChiayi Chang Gung Memorial Hospital · TWChung Shan Medical University · TWKing's College London · GB

Funding

Chiayi Chang Gung Memorial Hospital CMRPG6E0273Chung Shan Medical University Grant 104-CSMU37 and 104-CSMU38
6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is an aggressive cancer with poor prognosis. Although recent research has indicated that selective serotonin reuptake inhibitors (SSRIs), including escitalopram, have anticancer effects, little is known about the effects of escitalopram on HCC.

methodsBoth in vitro and in vivo studies were conducted to verify the potentials of escitalopram on HCC treatment. To explore whether the effects of escitalopram are clinically consistent with laboratory findings, a nationwide population-based cohort study was also adopted to examine the association between escitalopram and HCC risk.

resultsAs compared with THLE-3 cells, escitalopram significantly inhibited the proliferation of HepG2 and Huh-7 cells. Specifically, escitalopram significantly induced autophagy in HepG2 and Huh-7 cells by increasing the LC3-II/LC3-I ratio and the expression of ATG-3, ATG-5, ATG-7, and Beclin-1 proteins. Moreover, escitalopram significantly inhibited the growth of xenografted Huh-7 cells in SCID mice that were treated with 12.5 mg/kg escitalopram. Accordingly, the risk of HCC was negatively correlated with escitalopram use.

conclusionsThese findings provided evidence supporting the therapeutic potential of escitalopram for HCC. Both laboratory and nationwide population-based cohort evidence demonstrated the attenuated effects of escitalopram on HCC.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsAnimalsAutophagyCell Line, TumorCohort StudiesEscitalopramHumansMiceMice, SCIDEscitalopramautophagyescitalopramhepatocellular carcinoma (HCC)nationwide population-based cohort studyselective serotonin reuptake inhibitors (SSRIs)

Identifiers

PMID36012510
PMCPMC9408912
OpenAlexW4292164325

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.