Evidence map›Paper›PMID 31058847›Full record

ReviewMolecules (Basel, Switzerland)2019

Advances in the Antagonism of Epigallocatechin-3-gallate in the Treatment of Digestive Tract Tumors.

Changwei Liu, Penghui Li, Zhihao Qu, Wei Xiong, Ailing Liu, Sheng Zhang

Open access · goldAbstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Apoptotic-Induced Effects ofInternational journal of molecular sciences · 2020
    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

6 authors at 2 institutions in 1 country.

Changwei LiuKey Laboratory of Tea Science of Ministry of Education, Hunan Agricultural University, Changsha 410128, China. liuchangwvv@163.com.
Penghui LiKey Laboratory of Tea Science of Ministry of Education, Hunan Agricultural University, Changsha 410128, China. lpflstt111@163.com.
Zhihao QuKey Laboratory of Tea Science of Ministry of Education, Hunan Agricultural University, Changsha 410128, China. 18579546687@163.com.
Wei XiongThe Key Laboratory of Carcinogenesis and Cancer Invasion of the Chinese Ministry of Education, Cancer Research Institute, Central South University, Changsha 410078, China. xiongwei@csu.edu.cn.
Ailing LiuCollege of Bioscience and Biotechnology, Hunan Agricultural University, Changsha 410128, China. liuailing@hunau.edu.cn.
Sheng ZhangKey Laboratory of Tea Science of Ministry of Education, Hunan Agricultural University, Changsha 410128, China. zhangsheng@hunau.edu.cn.ORCID 0000-0003-2288-1120
Hunan Agricultural University · CNCentral South University · CN

Funding

Changsha Science and Technology Major Project kq1703003Natural Science Foundation of Hunan Province 2019JJ40120the National Key R&D Project 2017YFD0400803
6 · The paper itself

Abstract

Due to changes in the dietary structure of individuals, the incidence of digestive tract tumors has increased significantly in recent years, causing a serious threat to the life and health of patients. This has in turn led to an increase in cancer prevention research. Many studies have shown that epigallocatechin-3-gallate (EGCG), an active ingredient in green tea, is in direct contact with the digestive tract upon ingestion, which allows it to elicit a significant antagonizing effect on digestive tract tumors. The main results of EGCG treatment include the prevention of tumor development in the digestive tract and the induction of cell cycle arrest and apoptosis. EGCG can be orally administered, is safe, and combats other resistances. The synergistic use of cancer drugs can promote the efficacy and reduce the anti-allergic properties of drugs, and is thus, favored in medical research. EGCG, however, currently possesses several shortcomings such as poor stability and low bioavailability, and its clinical application prospects need further development. In this paper, we have systematically summarized the research progress on the ability of EGCG to antagonize the activity and mechanism of action of digestive tract tumors, to achieve prevention, alleviation, delay, and even treat human gastrointestinal tract tumors via exogenous dietary EGCG supplementation or the development of new drugs containing EGCG.

Indexed as

Administration, OralBiological AvailabilityCatechinCell CycleCell Line, TumorCell SurvivalDrug DiscoveryGastrointestinal NeoplasmsHumansTeaCatechinepigallocatechin gallateTeaanti-cancer therapyapoptosiscellular signaling cascadescolorectal cancerdigestive tract tumorepigallocatechin-3-gallate

Identifiers

PMID31058847
PMCPMC6539113
OpenAlexW2943197695

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.