Suetsugu Fumiyuki, Tadokoro Tomoko, Fujita Koji, Fujihara Shintaro, Sasaki Kota, Omayu Erika, Nakatani Kaho, Koyama Yukiko, Kozuka Kazuhiro, Matsui Takanori, Nakahara Mai, Oura Kyoko, Kitaoka Atsuo, Yachida Tatsuo, Tani Joji, Morishita Asahiro, Masaki Tsutomu, Kobara Hideki
Department of Gastroenterology and Neurology, Faculty of Medicine, Kagawa University, Kagawa, Japan.
Department of Gastroenterology and Neurology, Faculty of Medicine, Kagawa University, Kagawa, Japan
Anticancer Res. 2025 Jul;45(7):2937-2947. doi: 10.21873/anticanres.17661.
BACKGROUND/AIM: Tea consumption is widely reported to have beneficial effects on cancer prevention. Epigallocatechin-3-gallate (EGCG), a major bioactive component of green tea, has demonstrated anti-proliferative effects against various cancer cell types. This study aimed to evaluate the antitumor effects of EGCG on human colon and colorectal cancer cells both and and to identify microRNAs (miRNAs) associated with its antitumor activity.
We investigated the ability of EGCG to inhibit cell proliferation by apoptosis and analyzed its effects on cell cycle-related molecules in multiple human colon cancer cell lines. Additionally, EGCG-induced alterations in activated receptor tyrosine kinases and angiogenesis-related proteins were assessed using protein arrays. miRNA array analysis was performed to identify EGCG-regulated miRNAs. An mouse xenograft model was used to assess the tumor-suppressive potential of EGCG.
EGCG induced apoptosis and significantly suppressed the proliferation of colon cancer cells, both and . In the miRNA array analysis, EGCG-treated CW-2 cells exhibited up-regulation of seven miRNAs and down-regulation of eight miRNAs. Notably, the down-regulation of hsa-miR-187-5p was most significant.
EGCG suppresses the proliferation of human colon cancer cells through induction of apoptosis. Down-regulation of hsa-miR-187-5p may be a potential marker for the effect of EGCG in regulating colorectal cancer. These findings suggest that EGCG may serve as a promising therapeutic agent or adjunct in the treatment of colorectal cancer.
背景/目的:大量报道称饮茶对癌症预防有益。表没食子儿茶素没食子酸酯(EGCG)是绿茶的主要生物活性成分,已显示出对多种癌细胞类型具有抗增殖作用。本研究旨在评估EGCG对人结肠癌和结肠直肠癌细胞的抗肿瘤作用,并鉴定与其抗肿瘤活性相关的微小RNA(miRNA)。
我们研究了EGCG通过凋亡抑制细胞增殖的能力,并分析了其对多种人结肠癌细胞系中细胞周期相关分子的影响。此外,使用蛋白质阵列评估EGCG诱导的活化受体酪氨酸激酶和血管生成相关蛋白的变化。进行miRNA阵列分析以鉴定EGCG调节的miRNA。使用小鼠异种移植模型评估EGCG的肿瘤抑制潜力。
EGCG诱导凋亡并显著抑制结肠癌细胞的增殖。在miRNA阵列分析中,EGCG处理的CW-2细胞表现出7种miRNA上调和8种miRNA下调。值得注意的是,hsa-miR-187-5p的下调最为显著。
EGCG通过诱导凋亡抑制人结肠癌细胞的增殖。hsa-miR-187-5p的下调可能是EGCG调节结肠直肠癌作用的潜在标志物。这些发现表明EGCG可能成为治疗结肠直肠癌的有前景的治疗药物或辅助药物。