Evidence map›Paper›PMID 26199554›Full record

ArticleJournal of ginseng research2015

American ginseng significantly reduced the progression of high-fat-diet-enhanced colon carcinogenesis in Apc (Min/+) mice.

Chunhao Yu, Xiao-Dong Wen, Zhiyu Zhang, Chun-Feng Zhang, Xiaohui Wu, Xin He, Yang Liao, Ningning Wu, Chong-Zhi Wang, Wei Du and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of ginseng research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed, 23 citations in OpenAlex.

  1. Trial
  2. Colorectal cancer and microbiota: systematic review.Przeglad gastroenterologiczny · 2024
    Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Role of intestinal microbiome in American ginseng-mediated colon cancer prevention in high fat diet-fed AOM/DSS mice [corrected].Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2018
    Article
  8. Review
  9. Article
  10. Article
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

12 authors at 1 institution in 2 countries.

Chunhao YuSchool of Life Science and Chemical Engineering, Huaiyin Institute of Technology, Jiangsu, China ; Jiangsu Provincial Engineering Laboratory for Biomass Conversion and Process Integration, Huaiyin Institute of Technology, Jiangsu, China ; Tang Center for Herbal Medicine Research, University of Chicago, Chicago, IL, USA ; Department of Anesthesia and Critical Care, University of Chicago, Chicago, IL, USA.
Xiao-Dong WenTang Center for Herbal Medicine Research, University of Chicago, Chicago, IL, USA ; Department of Anesthesia and Critical Care, University of Chicago, Chicago, IL, USA.
Zhiyu ZhangTang Center for Herbal Medicine Research, University of Chicago, Chicago, IL, USA ; Department of Anesthesia and Critical Care, University of Chicago, Chicago, IL, USA.
Chun-Feng ZhangTang Center for Herbal Medicine Research, University of Chicago, Chicago, IL, USA ; Department of Anesthesia and Critical Care, University of Chicago, Chicago, IL, USA.
Xiaohui WuTang Center for Herbal Medicine Research, University of Chicago, Chicago, IL, USA ; Department of Anesthesia and Critical Care, University of Chicago, Chicago, IL, USA.
Xin HeTang Center for Herbal Medicine Research, University of Chicago, Chicago, IL, USA ; Department of Anesthesia and Critical Care, University of Chicago, Chicago, IL, USA.
Yang LiaoTang Center for Herbal Medicine Research, University of Chicago, Chicago, IL, USA ; Ben May Department for Cancer Research, University of Chicago, Chicago, IL, USA.
Ningning WuTang Center for Herbal Medicine Research, University of Chicago, Chicago, IL, USA ; Molecular Oncology Laboratory, Department of Surgery, University of Chicago Medical Center, Chicago, IL, USA.
Chong-Zhi WangTang Center for Herbal Medicine Research, University of Chicago, Chicago, IL, USA ; Department of Anesthesia and Critical Care, University of Chicago, Chicago, IL, USA.
Wei DuTang Center for Herbal Medicine Research, University of Chicago, Chicago, IL, USA ; Ben May Department for Cancer Research, University of Chicago, Chicago, IL, USA.
Tong-Chuan HeTang Center for Herbal Medicine Research, University of Chicago, Chicago, IL, USA ; Molecular Oncology Laboratory, Department of Surgery, University of Chicago Medical Center, Chicago, IL, USA.
Chun-Su YuanTang Center for Herbal Medicine Research, University of Chicago, Chicago, IL, USA ; Department of Anesthesia and Critical Care, University of Chicago, Chicago, IL, USA ; Committee on Clinical Pharmacology and Pharmacogenomics, University of Chicago, Chicago, IL, USA.
University of Chicago · US

Funding

Center for Herbal Research on Colorectal CancerP01AT004418 · NCCIH · UNIVERSITY OF CHICAGO · PI YUAN, CHUN-SU · 2008 to 2012
$5.9M
Chemoprevention of Active Scutellaria baicalensis Fraction on Colon CancerK01AT005362 · NCCIH · UNIVERSITY OF CHICAGO · PI WANG, CHONG-ZHI · 2010 to 2014
$486k
NCCIH NIH HHS K01 AT005362NCCIH NIH HHS P01 AT004418
6 · The paper itself

Abstract

backgroundColorectal cancer (CRC) is a leading cause of death worldwide. Chronic gut inflammation is recognized as a risk factor for tumor development, including CRC. American ginseng is a very commonly used ginseng species in the West.

methodsA genetically engineered Apc (Min/+) mouse model was used in this study. We analyzed the saponin composition of American ginseng used in this project, and evaluated its effects on the progression of high-fat-diet-enhanced CRC carcinogenesis.

resultsAfter oral ginseng administration (10-20 mg/kg/d for up to 32 wk), experimental data showed that, compared with the untreated mice, ginseng very significantly reduced tumor initiation and progression in both the small intestine (including the proximal end, middle end, and distal end) and the colon (all p < 0.01). This tumor number reduction was more obvious in those mice treated with a low dose of ginseng. The tumor multiplicity data were supported by body weight changes and gut tissue histology examinations. In addition, quantitative real-time polymerase chain reaction analysis showed that compared with the untreated group, ginseng very significantly reduced the gene expression of inflammatory cytokines, including interleukin-1α (IL-1α), IL-1β, IL-6, tumor necrosis factor-α, granulocyte-colony stimulating factor, and granulocyte-macrophage colony-stimulating factor in both the small intestine and the colon (all p < 0.01).

conclusionFurther studies are needed to link our observed effects to the actions of the gut microbiome in converting the parent ginsenosides to bioactive ginseng metabolites. Our data suggest that American ginseng may have potential value in CRC chemoprevention.

Indexed as

ApcMin/+micecolorectal cancerginsenoside metabolitesinflammatory cytokinesPanax quinquefolius L.

Identifiers

PMID26199554
PMCPMC4506368
OpenAlexW2143360088

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.