Evidence map›Paper›PMID 32750222›Full record

ArticleFEBS open bio2020

Vortioxetine induces apoptosis and autophagy of gastric cancer AGS cells via the PI3K/AKT pathway.

Gao-Bo Lv, Ting-Ting Wang, Hai-Lin Zhu, Hong-Ke Wang, Wen Sun, Li-Feng Zhao

Open access · goldAbstract read
In one paragraph

Article in FEBS open bio, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 30 citations in OpenAlex.

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  8. Targetable pathways for drug repurposing in gastric cancer.World journal of gastroenterology · 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

6 authors at 2 institutions in 1 country.

Gao-Bo LvDepartment of Anal-colorectal Surgery, Baoji Municipal Central Hospital, Baoji, China.
Ting-Ting WangDepartment of Administration Center Outpatient, Baoji Municipal Central Hospital, Baoji, China.
Hai-Lin ZhuDepartment of Hepatobiliary Pancreatic Surgery, Baoji Municipal Central Hospital, Baoji, China.
Hong-Ke WangDepartment of Gastroenterology, Baoji Municipal Central Hospital, Baoji, China.
Wen SunBeijing Splinger Institute of Medicine, Jinan, China.
Li-Feng ZhaoDepartment of Hepatobiliary Pancreatic Surgery, Baoji Municipal Central Hospital, Baoji, China.ORCID 0000-0002-6882-9128
Baoji City Central Hospital · CNJinling Institute of Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vortioxetine is a potent antagonist of the 5-hydroxytryptamine receptor and serotonin transporter and has been reported to function as an antidepressant in the treatment of major depressive disorder. However, its antitumor effects remain unclear. Here, we examined whether vortioxetine affects the characteristics of GC cells. Cell viability was measured by a colony formation assay and, in addition, cell invasion, migration and apoptosis assays were performed with a transwell assay and a flow cytometry assay. Protein levels were measured by western blotting. We found that vortioxetine inhibited the proliferation, invasion and migration abilities of AGS cells. Additionally, vortioxetine could induce apoptosis and autophagy by increasing the levels of Bax, active caspase-3/-9, Beclin-1 and light chain 3, as well as by downregulating Bcl-2 and P62. Further investigations indicated that vortioxetine regulated apoptosis and autophagy via activation of the phosphoinositide 3-kinase/AKT pathway. Taken together, our data suggest that vortioxetine has cytotoxic effects against GC AGS cells as a result of inhibiting proliferation, invasion and migration, as well as by inducing apoptosis and autophagy through the phosphoinositide 3-kinase/AKT pathway.

Indexed as

ApoptosisAutophagyCell DeathCell Line, TumorCell ProliferationCell SurvivalChinaHumansNeoplasm InvasivenessPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionStomach NeoplasmsVortioxetinePhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktVortioxetineapoptosisautophagygastric cancerPI3K/AKT pathwaytumorigenicityvortioxetine

Identifiers

PMID32750222
PMCPMC7530385
OpenAlexW3047296368

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.