Evidence map›Paper›PMID 33437164›Full record

ArticleJournal of ginseng research2021

Ginsenoside 20(S)-protopanaxadiol induces cell death in human endometrial cancer cells via apoptosis.

Hantae Jo, Dongmin Jang, Sun Kyu Park, Mi-Gi Lee, Byungsun Cha, Chaewon Park, Yong Sub Shin, Hyein Park, Jin-Myoung Baek, Hyojin Heo and 7 more

Open access · goldAbstract read
In one paragraph

Article in Journal of ginseng research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

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  17. Phytochemicals in Gynecological Cancer Prevention.International journal of molecular sciences · 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

17 authors at 6 institutions in 1 country.

Hantae JoDepartment of Biological Sciences, Ajou University, Suwon, Republic of Korea.
Dongmin JangDepartment of Biomedical Sciences, Graduate Program of Molecular Medicine, Ajou University Graduate School of Medicine, Suwon, Republic of Korea.
Sun Kyu ParkDepartment of Conservative Dentistry, Gangnam Severance Hospital, Yonsei University College of Dentistry, Seoul, Republic of Korea.
Mi-Gi LeeGyeonggido Business and Science Accelerator, Suwon, Republic of Korea.
Byungsun ChaDepartment of Applied Biotechnology, Ajou University Graduate School, Suwon, Republic of Korea.
Chaewon ParkDepartment of Applied Biotechnology, Ajou University Graduate School, Suwon, Republic of Korea.
Yong Sub ShinGraduate School of Biotechnology, Kyung Hee University, Yongin, Republic of Korea.
Hyein ParkDepartment of Applied Biotechnology, Ajou University Graduate School, Suwon, Republic of Korea.
Jin-Myoung BaekDepartment of Applied Biotechnology, Ajou University Graduate School, Suwon, Republic of Korea.
Hyojin HeoDepartment of Applied Biotechnology, Ajou University Graduate School, Suwon, Republic of Korea.
Sofia BritoDepartment of Applied Biotechnology, Ajou University Graduate School, Suwon, Republic of Korea.
Hyun Gyu HwanCollege of Pharmacy, Seoul National University, Seoul, Republic of Korea.
Sehyun ChaeKorea Brain Bank, Korea Brain Research Institute, Daegu, Republic of Korea.
Shao-Wei YanDepartment of Applied Biotechnology, Ajou University Graduate School, Suwon, Republic of Korea.
Changho LeeDepartment of Pharmacology and Biomedical Science, College of Medicine, Hanyang University, Seoul, Republic of Korea.
Churl K MinDepartment of Biological Sciences, Ajou University, Suwon, Republic of Korea.
Bum-Ho BinDepartment of Biological Sciences, Ajou University, Suwon, Republic of Korea.
Ajou University · KRGangnam Severance Hospital · KRHanyang University · KRKorea Brain Research Institute · KRKyung Hee University · KRSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background20(S)-protopanaxadiol (20(S)-PPD), one of the aglycone derivatives of major ginsenosides, has been shown to have an anticancer activity toward a variety of cancers. This study was initiated with an attempt to evaluate its anti-cancer activity toward human endometrial cancer by cell and xenograft mouse models.

methodsHuman endometrial cancer (HEC)-1A cells were incubated with different 20(S)-PPD concentrations. 20(S)-PPD cytotoxicity was evaluated using MTT assay. Apoptosis was detected using the annexin V binding assay and cell cycle analysis. Cleaved poly (ADP-ribose) polymerase (PARP) and activated caspase-9 were assessed using western blotting. HEC-1A cell tumor xenografts in athymic mice were generated by inoculating HEC-1A cells into the flank of BALB/c female mice and explored to validate 20(S)-PPD anti-endometrial cancer toxicity.

results20(S)-PPD inhibited HEC-1A cell proliferation in a dose-dependent manner with an IC

conclusion20(S)-PPD inhibits endometrial cancer cell proliferation by inducing cell death via a caspase-mediated apoptosis pathway. Therefore, the 20(S)-PPD-like ginsenosides are endowed with ample structural information that could be utilized to develop other ginsenoside-based anticancer agents.

Indexed as

20(S)-PPDapoptosisathymic miceendometrial cancerxenograft

Identifiers

PMID33437164
PMCPMC7790893
OpenAlexW3038859202

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.