Agarwal Anshu, Kansal Vikash, Farooqi Humaira, Prasad Ram, Singh Vijay Kumar
Department of Zoology, Agra College, Dr. Bhimrao Ambedkar University, Agra 282004, India.
Department of Otolaryngology, Emory University, Atlanta, GA 30322, USA.
Biomedicines. 2023 Mar 5;11(3):789. doi: 10.3390/biomedicines11030789.
Head and neck cancers are among the deadliest cancers, ranked sixth globally in rates of high mortality and poor patient prognoses. The prevalence of head and neck squamous cell carcinoma (HNSCC) is associated with smoking and excessive alcohol consumption. Despite several advances in diagnostic and interventional methods, the morbidity of subjects with HNSCC has remained unchanged over the last 30 years. Epigenetic alterations, such as DNA hypermethylation, are commonly associated with several cancers, including HNSCC. Thus, epigenetic changes are considered promising therapeutic targets for chemoprevention. Here, we investigated the effect of EGCG on DNA hypermethylation and the growth of HNSCC. First, we assessed the expression levels of global DNA methylation in HNSCC cells (FaDu and SCC-1) and observed enhanced methylation levels compared with normal human bronchial epithelial cells (NHBE). Treatment of EGCG to HNSCC cells significantly inhibited global DNA hypermethylation by up to 70-80% after 6 days. Inhibition of DNA hypermethylation in HNSCC cells was confirmed by the conversion of 5-methylcytosine (5-mc) into 5-hydroxy methylcytosine (5hmC). DNA methyltransferases regulate DNA methylation. Next, we checked the effect of EGCG on the expression levels of DNA methyltransferases (DNMTs) and DNMT activity. Treatment of EGCG to HNSCC cells significantly reduced DNMT activity to 60% in SCC-1 and 80% in FaDu cells. The protein levels of DNMT3a and DNMT3b were downregulated in both cell lines after EGCG treatment. EGCG treatment to HNSCC cells reactivated tumor suppressors and caused decreased cell proliferation. Our in vivo study demonstrated that administration of EGCG (0.5%, /) as a supplement within an AIN76A diet resulted in inhibition of tumor growth in FaDu xenografts in nude mice (80%; < 0.01) compared with non-EGCG-treated controls. The growth inhibitory effect of dietary EGCG on the HNSCC xenograft tumors was associated with the inhibition of DNMTs and reactivation of silenced tumor suppressors. Together, our study provides evidence that EGCG acts as a DNA demethylating agent and can reactivate epigenetically silenced tumor suppressors to inhibit the growth of HNSCC cells.
头颈癌是最致命的癌症之一,在全球高死亡率和患者预后不良的癌症中排名第六。头颈部鳞状细胞癌(HNSCC)的患病率与吸烟和过量饮酒有关。尽管在诊断和介入方法方面取得了一些进展,但在过去30年中,HNSCC患者的发病率一直保持不变。表观遗传改变,如DNA高甲基化,通常与包括HNSCC在内的几种癌症有关。因此,表观遗传变化被认为是化学预防的有前景的治疗靶点。在这里,我们研究了表没食子儿茶素没食子酸酯(EGCG)对DNA高甲基化和HNSCC生长的影响。首先,我们评估了HNSCC细胞(FaDu和SCC-1)中整体DNA甲基化的表达水平,并观察到与正常人支气管上皮细胞(NHBE)相比甲基化水平有所提高。用EGCG处理HNSCC细胞6天后,显著抑制整体DNA高甲基化达70%-80%。通过将5-甲基胞嘧啶(5-mc)转化为5-羟甲基胞嘧啶(5hmC),证实了HNSCC细胞中DNA高甲基化的抑制。DNA甲基转移酶调节DNA甲基化。接下来,我们检查了EGCG对DNA甲基转移酶(DNMTs)表达水平和DNMT活性的影响。用EGCG处理HNSCC细胞后,SCC-1细胞中的DNMT活性显著降低至60%,FaDu细胞中的DNMT活性降低至80%。EGCG处理后,两种细胞系中DNMT3a和DNMT3b的蛋白水平均下调。用EGCG处理HNSCC细胞可重新激活肿瘤抑制因子并导致细胞增殖减少。我们的体内研究表明,在AIN76A饮食中添加EGCG(0.5%,/)可抑制裸鼠FaDu异种移植瘤的生长(80%;<0.01),与未用EGCG处理的对照组相比。饮食中的EGCG对HNSCC异种移植瘤的生长抑制作用与DNMTs的抑制和沉默肿瘤抑制因子的重新激活有关。总之