Evidence map›Paper›PMID 34257801›Full record

ArticleOxidative medicine and cellular longevity2021

Ginsenoside Rg5 Inhibits Human Osteosarcoma Cell Proliferation and Induces Cell Apoptosis through PI3K/Akt/mTORC1-Related LC3 Autophagy Pathway.

Ming-Yang Liu, Fei Liu, Yan-Jiao Li, Jia-Ning Yin, Yan-Li Gao, Xin-Yue Wang, Chen Yang, Jian-Guo Liu, Hai-Jun Li

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 30 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

9 authors at 1 institution in 1 country.

Ming-Yang LiuDepartment of Immunity, Institute of Translational Medicine, The First Hospital of Jilin University, China.
Fei LiuDepartment of Obstetrics, The First Hospital of Jilin University, China.
Yan-Jiao LiDepartment of Pharmacy, The First Hospital of Jilin University, China.
Jia-Ning YinDepartment of Pediatrics, The First Hospital of Jilin University, China.
Yan-Li GaoDepartment of Pediatrics, The First Hospital of Jilin University, China.
Xin-Yue WangDepartment of Scientific Research, College of Basic Medicine, Jilin University, China.
Chen YangDepartments of Orthopaedics, The First Hospital of Jilin University, China.
Jian-Guo LiuDepartments of Orthopaedics, The First Hospital of Jilin University, China.
Hai-Jun LiDepartment of Immunity, Institute of Translational Medicine, The First Hospital of Jilin University, China.ORCID https://orcid.org/0000-0002-2515-3076
Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The function and mechanism underlying the suppression of human osteosarcoma cells by ginsenoside-Rg5 (Rg5) was investigated in the present study. MG-63, HOS, and U2OS cell proliferation was determined by MTT assay after Rg5 treatment for 24 h. Rg5 inhibited human osteosarcoma cell proliferation effectively in a dose-dependent manner. The range of effective inhibitory concentrations was 160-1280 nM. Annexin V-FITC and PI double-staining assay revealed that Rg5 induced human osteosarcoma cell apoptosis. Western blotting, qRT-PCR, and FACS experiments revealed that Rg5 inhibited human osteosarcoma cells via caspase-3 activity which was related to the LC3-mediated autophagy pathway. Rg5 decreased the phosphorylation of PI3K, Akt, and mTORC1 activation. In contrast, LC3-mediated autophagy and caspase-3 activity increased significantly. A PI3K/AKT stimulator, IGF-1, reversed Rg5-induced cell autophagy and apoptosis in MG-63 cells. Collectively, the current study demonstrated that Rg5 induced human osteosarcoma cell apoptosis through the LC3-mediated autophagy pathway. Under physiological conditions, activation of PI3K/AKT/mTORC1 inhibits LC3 activity and caspase-3-related cell apoptosis. However, Rg5 activated LC3 activity by inhibiting the activation of PI3K/AKT/mTORC1. The present study indicated that Rg5 could be a promising candidate as a chemotherapeutic agent against human osteosarcoma.

Indexed as

ApoptosisAutophagyCell Line, TumorCell ProliferationGinsenosidesHumansOsteosarcomaPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionGinsenosidesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-akt

Identifiers

PMID34257801
PMCPMC8257372
OpenAlexW3175670325

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.