Tea polyphenol EGC suppresses colorectal cancer cell proliferation both in vitro and in vivo via downregulation of STAT3

[Display omitted] •EGC inhibited colorectal cancer SW480, SW620 and LS411N cell proliferation by induction of apoptosis.•EGC suppressed colon cancer cell migration and inhibited the phosphorylated STAT3 (p-STAT3) expression by inhibition STAT3 promoter activity and suppression STAT3 transcription.•E...

Full description

Saved in:
Bibliographic Details
Published in:Journal of functional foods Vol. 112; p. 105977
Main Authors: Luo, Ke-Wang, Ye, Wei, Li, Ning, Cheng, Bao-Hui
Format: Journal Article
Language:English
Published: Elsevier Ltd 01-01-2024
Elsevier
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:[Display omitted] •EGC inhibited colorectal cancer SW480, SW620 and LS411N cell proliferation by induction of apoptosis.•EGC suppressed colon cancer cell migration and inhibited the phosphorylated STAT3 (p-STAT3) expression by inhibition STAT3 promoter activity and suppression STAT3 transcription.•EGC decreased tumor growth in animal via down regulation of phosphorylated S TAT3.•EGC also led to inhibition of proliferation and activity in colorectal tumor organoids. Epigallocatechin (EGC) is one of the main bioactive polyphenols in green tea. This study aims to determine the anti-tumor effect of EGC against colorectal cancer. Our results revealed that treatment of EGC led to significant suppression of cell proliferation and apoptosis in three colorectal cancer cells. Western blot confirmed that EGC activated Caspase-3 and PARP, down-regulated the phosphorylation of STAT3 and decreased Bcl-2 expression. Luciferase-reporter-activity assay further determined that EGC suppressed the promoter activity of STAT3 and downregulated the transcription of STAT3. Besides, in vivo study proved that EGC (100 mg/kg) resulted in significant suppression of tumor volume and tumor weight (decreased by 63.7 %) in mice bearing SW620 tumors. Tumor organoid assays demonstrated the inhibitory efficacy of EGC in colorectal organoids. In conclusion, our study present evidence that EGC inhibited colon cancer cell proliferation both in vitro and in vivo by down-regulation phosphorylated STAT3 and activated downstreams.
ISSN:1756-4646
2214-9414
DOI:10.1016/j.jff.2023.105977