Department of Otolaryngology, Mackay Memorial Hospital, Taipei, Taiwan; School of Medicine, Mackay Medical College, New Taipei City, Taiwan.
Department of Anatomy, College of Medicine, Chang Gung University, Tao-Yuan, Taiwan.
Cancer Lett. 2015 May 1;360(2):310-8. doi: 10.1016/j.canlet.2015.02.034. Epub 2015 Feb 23.
Oral squamous cell carcinoma (OSCC) is a well-known malignancy that accounts for the majority of oral cancers. B-cell translocation gene 2 (BTG2) is an important regulator of cell cycle dynamics in cancer cells. However, the role of BTG2 in OSCC cells and the influences of epigallocatechin-3-gallate (EGCG) on BTG2 gene expressions have not been well evaluated. The objectives of this study were to examine the effect of EGCG-induced BTG2 expression and the potential signal pathways involved. The (3)H-thymidine incorporation and Western-blot assays revealed cell proliferation was attenuated by EGCG via upregulation of BTG2 expression causing cell cycle G1 phase arrest in OSCC cells. BTG2 overexpression decreased tumor cell growth, while BTG2 knockdown illuminated the opposite effect in xenograft animal studies. Overexpressed BTG2 arrested the cell cycle at the G1 phase and downregulated protein expressions of cyclin A, cyclin D, and cyclin E. Western-blot assays indicated that EGCG induced phosphorylation of p38, JNK, and ERK. However, pretreatments with selective mitogen-activated protein kinase (MAPK) inhibitors, SB203580 (p38 inhibitor) and PD0325901 (ERK1/2 inhibitor), significantly suppressed the activation of EGCG on BTG2 expression. Our results indicate that EGCG attenuates cell proliferation of OSCC cells by upregulating BTG2 expression via p38 and ERK pathways.
口腔鳞状细胞癌(OSCC)是一种众所周知的恶性肿瘤,占口腔癌的大多数。B 细胞易位基因 2(BTG2)是癌细胞细胞周期动力学的重要调节剂。然而,BTG2 在 OSCC 细胞中的作用以及表没食子儿茶素没食子酸酯(EGCG)对 BTG2 基因表达的影响尚未得到很好的评估。本研究旨在探讨 EGCG 诱导的 BTG2 表达的作用及其潜在的信号通路。(3)H-胸腺嘧啶掺入和 Western-blot 分析显示,EGCG 通过上调 BTG2 表达来抑制 OSCC 细胞的细胞增殖,导致细胞周期 G1 期停滞。BTG2 的过表达降低了肿瘤细胞的生长,而 BTG2 的敲低在异种移植动物研究中则显示出相反的效果。过表达的 BTG2 将细胞周期阻滞在 G1 期,并下调细胞周期蛋白 A、D 和 E 的蛋白表达。Western-blot 分析表明,EGCG 诱导 p38、JNK 和 ERK 的磷酸化。然而,用选择性丝裂原活化蛋白激酶(MAPK)抑制剂 SB203580(p38 抑制剂)和 PD0325901(ERK1/2 抑制剂)预处理显著抑制了 EGCG 对 BTG2 表达的激活。我们的结果表明,EGCG 通过 p38 和 ERK 通路上调 BTG2 表达来抑制 OSCC 细胞的增殖。