Evidence map›Paper›PMID 27186294›Full record

ArticleAmerican journal of translational research2016

The antitumor activity study of ginsenosides and metabolites in lung cancer cell.

Feng-Yuan Xu, Wen-Qing Shang, Jia-Jun Yu, Qian Sun, Ming-Qing Li, Jian-Song Sun

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 44 citations in OpenAlex.

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  10. Anti-inflammatory cytokines in endometriosis.Cellular and molecular life sciences : CMLS · 2019
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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 2 countries.

Feng-Yuan XuNational Engineering Research Center of Chemical Synthesis of Monosaccharide, Jiangxi Normal UniversityNanchang, Jiangxi Province 330027, People's Republic of China; Department of Chemistry, High School Affiliated to Shanghai Jiaotong UniversityShanghai 200493, People's Republic of China.
Wen-Qing ShangLaboratory for Reproductive Immunology, Hospital of Obstetrics and Gynecology, Fudan University Shanghai Medical College Shanghai 200011, People's Republic of China.
Jia-Jun YuLaboratory for Reproductive Immunology, Hospital of Obstetrics and Gynecology, Fudan University Shanghai Medical College Shanghai 200011, People's Republic of China.
Qian SunYerkes National Primate Research Center, Emory University Atlanta, GA 30329, USA.
Ming-Qing LiLaboratory for Reproductive Immunology, Hospital of Obstetrics and Gynecology, Fudan University Shanghai Medical CollegeShanghai 200011, People's Republic of China; Shanghai Key Laboratory of Female Reproductive Endocrine Related DiseasesShanghai 200011, People's Republic of China.
Jian-Song SunNational Engineering Research Center of Chemical Synthesis of Monosaccharide, Jiangxi Normal University Nanchang, Jiangxi Province 330027, People's Republic of China.
Shanghai Medical College of Fudan University · CNJiangxi Normal University · CNOregon National Primate Research Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ginseng and its components exert various biological effects, including antioxidant, anti-carcinogenic, anti-mutagenic, and antitumor activity. Ginsenosides are the main biological components of ginseng. Protopanaxadiol (PPD) and protopanaxatriol (PPT) are two metabolites of ginsenosides. However, the difference between these compounds in anti-lung cancer is unclear. The present study aimed to evaluate the antitumor activity of PPD, PPT, Ginsenosides-Rg3 (G-Rg3) and Ginsenosides-Rh2 (G-Rh2) in lung cancer cell. After treatment with cisplatin, PPD, PPT, G-Rg3 or G-Rh2, the viability, apoptosis level and invasiveness of lung cell lines (A549 cell, a lung adenocarcinoma cell line and SK-MES-1 cell, a lung squamous cell line) in vitro were analyzed by Cell Counting Kit-8 (CCK8), Annexin V/PI apoptosis and Matrigel invasion assays, respectively. Here we found that all these compounds led to significant decreases of viability and invasiveness and an obvious increase of apoptosis of A549 and SK-MES-1 cells. Among these, the viability of SK-MES-1 cell treated with PPT was decreased to 66.8%, and this effect was closest to Cisplatin. G-Rg3 had the highest stimulatory effect on apoptosis, and PTT had the highest inhibitory effect on cell invasiveness in A549 and SK-MES-1 cells. These results indicate that both ginsenosides and two metabolites have antitumor activity on lung cancer cell in vitro. However, PPT is more powerful for inhibiting the viability and invasiveness of lung cancer cell, especially lung squamous cell. G-Rg3 has the best pro-apoptosis effects. This study provides a scientific basis for potential therapeutic strategies targeted to lung cancer by further structure modification.

Indexed as

antitumor activityGinsenosideslung cancer cellPPDPPT

Identifiers

PMID27186294
PMCPMC4859899
OpenAlexW2474906923

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.