Evidence map›Paper›PMID 30942438›Full record

ArticleMolecular medicine reports2019

Ginsenoside Rg5 induces apoptosis in human esophageal cancer cells through the phosphoinositide‑3 kinase/protein kinase B signaling pathway.

Daoming Zhang, Aifu Wang, Jueping Feng, Qi Zhang, Linlin Liu, Hui Ren

Open access · hybridAbstract read
In one paragraph

Article in Molecular medicine reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

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  11. Pharmacological activities of ginsenoside Rg5 (Review).Experimental and therapeutic medicine · 2021
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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 3 institutions in 1 country.

Daoming ZhangDepartment of Radiotherapy, The Second Hospital of Jilin University, Changchun, Jilin 130041, P.R. China.
Aifu WangDepartment of Radiotherapy, The Second Hospital of Jilin University, Changchun, Jilin 130041, P.R. China.
Jueping FengDepartment of Oncology, Wuhan Puai Hospital of Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430035, P.R. China.
Qi ZhangDepartment of Radiotherapy, The Second Hospital of Jilin University, Changchun, Jilin 130041, P.R. China.
Linlin LiuDepartment of Radiotherapy, The Second Hospital of Jilin University, Changchun, Jilin 130041, P.R. China.
Hui RenDepartment of General Surgery, The China‑Japan Union Hospital of Jilin University, Changchun, Jilin 130000, P.R. China.
Second Affiliated Hospital of Jilin University · CNHuazhong University of Science and Technology · CNJilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role of ginsenoside in the prevention of cancer has been well established. Ginsenoside Rg5 is one of the main components isolated from red ginseng, which has been demonstrated to have anti‑tumor effects by inhibiting cell proliferation and causing DNA damage. However, the role of ginsenoside Rg5 and its molecular mechanisms remain unclear in human esophageal cancer. In the present study, Rg5 was investigated as a novel drug for the chemotherapy of esophageal cancer in in vitro experiments. Esophageal cancer Eca109 cells were exposed to various concentrations of ginsenoside Rg5 (0‑32 µΜ) for 24 h. Subsequent cell proliferation assays demonstrated that treatment with ginsenoside Rg5 resulted in the dose‑dependent inhibition of proliferation, while a significant increase in apoptotic rate and increased activities of caspase‑3, ‑8 and ‑9 were observed. In addition, the mitochondrial membrane potential was decreased and the cytoplasmic free calcium level increased following treatment with ginsenoside Rg5. Furthermore, the expression of B‑cell lymphoma 2 and phosphorylated‑protein kinase B (p‑Akt) decreased. The specific phosphoinositide‑3 kinase (PI3K) inhibitor LY294002 promoted this effect, while insulin‑like growth factor‑1, a specific PI3K activator, inhibited this action. Taken together, the results suggested that ginsenoside Rg5 may have a tumor‑suppressive effect on esophageal cancer by promoting apoptosis and may be associated with the downregulation of the PI3K/Akt signaling pathway.

Indexed as

ApoptosisCalciumCaspase 3Cell Line, TumorChromonesGinsenosidesHumansMembrane Potential, MitochondrialMorpholinesPhosphatidylinositol 3-KinasesPhosphorylationPoly(ADP-ribose) PolymerasesProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-bcl-2Signal Transduction2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-oneCalciumCaspase 3Chromonesginsenoside Rg5GinsenosidesMorpholinesPhosphatidylinositol 3-KinasesPoly(ADP-ribose) PolymerasesProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-bcl-2

Identifiers

PMID30942438
PMCPMC6471319
OpenAlexW2925117916

What OpenQuestion holds

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Registered trials

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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.