Evidence map›Paper›PMID 18549879›Full record

ArticleGastroenterology2008

A green tea component suppresses posttranslational expression of basic fibroblast growth factor in colorectal cancer.

Mugdha Sukhthankar, Kiyoshi Yamaguchi, Seong-Ho Lee, Michael F McEntee, Thomas E Eling, Yukihiko Hara, Seung Joon Baek

Open access · bronzeAbstract read
In one paragraph

Article in Gastroenterology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Pooled it
  2. New insights into the role of ubiquitination in angiogenesis (Review).International journal of molecular medicine · 2025
    Review
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  6. Article
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  8. Review
  9. Article
  10. Article
  11. Review
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  13. Effects of tea polyphenols on proliferation and apoptosis of cadmium-transformed cells.International journal of clinical and experimental medicine · 2015
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Phytochemicals and colorectal cancer prevention--myth or reality?Nature reviews. Gastroenterology & hepatology · 2011
    Article
  19. Review
  20. 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

7 authors at 2 institutions in 1 country.

Mugdha SukhthankarLaboratory of Environmental Carcinogenesis, Department of Pathobiology, College of Veterinary Medicine, University of Tennessee, Knoxville, Tennessee 37996, USA.
Kiyoshi Yamaguchi
Seong-Ho Lee
Michael F McEntee
Thomas E Eling
Yukihiko Hara
Seung Joon Baek
University of Tennessee at Knoxville · USResearch Triangle Park Foundation · US

Funding

Anti-carcinogenic Activity Of Cox inhibitors and NAG-1ZIAES010016 · NIEHS · NATIONAL INSTITUTE OF ENVIRONMENTAL HEALTH SCIENCES · PI ELING, THOMAS · 2009 to 2013
$8.3M
Murine Intestinal Tumorigenesis and PathobiologyK26RR016645 · NCRR · UNIVERSITY OF TENNESSEE KNOXVILLE · PI MCENTEE, MICHAEL F · 2001 to 2005
$485k
Anti-cancer effects by the green tea catechinsR21CA109423 · NCI · UNIVERSITY OF TENNESSEE KNOXVILLE · PI BAEK, SEUNG JOON · 2005 to 2006
$337k
NCI NIH HHS R21 CA109423NCI NIH HHS R21CA109423NCRR NIH HHS K26 RR016645NCRR NIH HHS K26RR016645
6 · The paper itself

Abstract

BACKGROUND &

aimsGreen tea catechins are known to have anticarcinogenic effects. Epigallocatechin-3-gallate (EGCG) accounts for almost 50% of the total catechin content in green tea extract and has very potent antioxidant effects. EGCG also inhibits angiogenesis, possibly through the inhibition of proangiogenic factors including vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF), which in turn, inhibits tumor growth and metastasis. However, the exact molecular mechanism by which EGCG suppresses bFGF expression is not known. Our objective was to elucidate the molecular mechanisms by which EGCG inhibits bFGF expression in colorectal cancer.

methodsWe examined posttranslational regulation of bFGF by EGCG in human colorectal cancer cells. We also examined bFGF in intestinal tumor formation of APC(Min/+) mice with and without catechin treatment.

resultsThe bFGF protein was quickly degraded in the presence of EGCG, but a proteasome inhibitor suppressed this degradation. EGCG was also found to increase ubiquitination of bFGF and trypsin-like activity of the 20S proteasome, thereby resulting in the degradation of bFGF protein. Furthermore, EGCG suppressed tumor formation in APC(Min/+) mice, compared with vehicle-treated mice, in association with reduced bFGF expression.

conclusionsThe ubiquitin-proteasome degradation pathway contributes significantly to down-regulation of bFGF expression by EGCG. Catechin compounds have fewer adverse effects than chemotherapeutic agents and hence can be used as proof-of-concept in cancer therapeutics to suppress growth and metastasis by targeting proteins such as bFGF.

Indexed as

Camellia sinensisAcetylcysteineAdenomatous Polyposis ColiAnimalsAntineoplastic Agents, PhytogenicCatechinCell Transformation, NeoplasticColorectal NeoplasmsCycloheximideCysteine Proteinase InhibitorsDisease Models, AnimalDose-Response Relationship, DrugDown-RegulationFibroblast Growth Factor 2Genes, APCHCT116 CellsAcetylcysteineAntineoplastic Agents, PhytogenicCatechinCycloheximideCysteine Proteinase Inhibitorsepigallocatechin gallateFibroblast Growth Factor 2lactacystinProteasome Endopeptidase ComplexProteasome InhibitorsProtein Synthesis Inhibitors

Identifiers

PMID18549879
PMCPMC2562743
OpenAlexW2052234372

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.