Evidence map›Paper›PMID 26702935›Full record

ArticleJournal of cancer research and clinical oncology2016

Naringin, a natural dietary compound, prevents intestinal tumorigenesis in Apc (Min/+) mouse model.

Yu-Sheng Zhang, Ye Li, Yan Wang, Shi-Yue Sun, Tao Jiang, Cong Li, Shu-Xiang Cui, Xian-Jun Qu

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Review
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  7. Article
  8. Intestinal CaWorld journal of gastroenterology · 2020
    Review
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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

8 authors at 4 institutions in 1 country.

Yu-Sheng ZhangSchool of Pharmaceutical Sciences, Shandong University, Jinan, China.
Ye LiDepartment of Pharmacology, School of Chemical Biology & Pharmaceutical Sciences, Capital Medical University, Beijing, China.
Yan WangDepartment of Pharmacology, Institute of Materia Medica, Shandong Academy of Medical Sciences, Jinan, China.
Shi-Yue SunDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Tao JiangShandong Tumor Hospital, Jinan, China.
Cong LiDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Shu-Xiang CuiDepartment of Pharmacology, School of Basic Medical Sciences, Capital Medical University, Beijing, China.
Xian-Jun QuSchool of Pharmaceutical Sciences, Shandong University, Jinan, China. quxj@ccmu.edu.cn.
Capital Medical University · CNShandong First Medical University · CNShandong Tumor Hospital · CNShandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeNaringin is a natural dietary flavonoid compound. We aimed to evaluate the effects of naringin on intestinal tumorigenesis in the adenomatous polyposis coli multiple intestinal neoplasia (Apc (Min/+)) mouse model.

methodsApc (Min/+) mice were given either naringin (150 mg/kg) or vehicle by p.o. gavage daily for 12 consecutive weeks. Mice were killed with ether, and blood samples were collected to assess the concentrations of IL-6 and PGE2. Total intestines were removed, and the number of polyps was examined. Tissue samples of intestinal polyps were subjected to the assays of histopathology, immunohistochemical analysis and Western blotting analysis.

resultsApc (Min/+) mice fed with naringin developed less and smaller polyps in total intestines. Naringin prevented intestinal tumorigenesis without adverse effects. Histopathologic analysis revealed the reduction of dysplastic cells and dysplasia in the adenomatous polyps. The treatments' effects might arise from its anti-proliferation, induction of apoptosis and modulation of GSK-3β and APC/β-catenin signaling pathways. Naringin also exerted its effects on tumorigenesis through anti-chronic inflammation.

conclusionNaringin prevented intestinal tumorigenesis likely through a collection of activities including anti-proliferation, induction of apoptosis, modulation of GSK-3β and APC/β-catenin pathways and anti-inflammation. Naringin is a potential chemopreventive agent for reducing the risk of colonic cancers.

Indexed as

Dietary SupplementsDisease Models, AnimalAdenomatous Polyposis Coli ProteinAnimalsApoptosisBlotting, WesternCell ProliferationCell Transformation, NeoplasticCytokinesFemaleFlavanonesHumansImmunoenzyme TechniquesInflammation MediatorsIntestinal NeoplasmsIntestinal PolypsAdenomatous Polyposis Coli ProteinCytokinesFlavanonesInflammation MediatorsnaringinAnti-inflammationAnti-proliferationApc Min/+ mouse modelAPC/β-catenin signaling pathwayApoptosisIntestinal adenomatous polypsNaringin

Identifiers

PMID26702935
PMCPMC11819250
OpenAlexW2275879912

What OpenQuestion holds

Textmetadata
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.