Prasad Ram, Katiyar Santosh K
Department of Dermatology, University of Alabama at Birmingham, Birmingham, AL, USA.
Department of Dermatology, University of Alabama at Birmingham, Birmingham, AL, USA ; Environmental Health Sciences, University of Alabama at Birmingham, Birmingham, AL, USA ; Nutrition Obesity Research Center, School of Public Health, University of Alabama at Birmingham, Birmingham, AL, USA ; Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, USA ; Birmingham Veterans Affairs Medical Center, Birmingham, AL, USA.
Genes Cancer. 2015 Jan;6(1-2):49-61. doi: 10.18632/genesandcancer.52.
Melanoma is the leading cause of skin cancer-related deaths. We have examined the effect of green tea polyphenols (GTPs), a natural mixture of epicatechin monomers, on melanoma cancer cell growth and the molecular mechanism underlying these effects using different human melanoma cell lines as an in vitro model. Treatment of melanoma cell lines (A375, Hs294t, SK-Mel28 and SK-Mel119) with GTPs significantly inhibited the cell viability as well as colony formation ability of melanoma cells in a dose-dependent manner. These effects of GTPs were associated with a significant inhibition of histone deacetylase (HDAC) activity, reduction in the levels of class I HDAC proteins, enhancement of histone acetyltransferase (HAT) activity and induction of DNA damage, as detected by Comet assay, in melanoma cells. GTPs-induced decrease in the levels of class I HDAC proteins is mediated through proteasomal degradation. Valproic acid, an inhibitor of HDACs, exhibited a similar pattern of reduced viability and induction of death of melanoma cells. Treatment of A375 and Hs294t cells with GTPs resulted in a decrease in the levels of cyclins and cyclin dependent kinases of G1 phase of cell cycle whereas upregulated the levels of tumor suppressor proteins (Cip1/WAF1/p21, p16 and p53).
黑色素瘤是皮肤癌相关死亡的主要原因。我们使用不同的人黑色素瘤细胞系作为体外模型,研究了绿茶多酚(GTPs)(一种表儿茶素单体的天然混合物)对黑色素瘤癌细胞生长的影响以及这些影响背后的分子机制。用GTPs处理黑色素瘤细胞系(A375、Hs294t、SK-Mel28和SK-Mel119)可显著抑制黑色素瘤细胞的活力以及集落形成能力,且呈剂量依赖性。GTPs的这些作用与组蛋白去乙酰化酶(HDAC)活性的显著抑制、I类HDAC蛋白水平的降低、组蛋白乙酰转移酶(HAT)活性的增强以及通过彗星试验检测到的黑色素瘤细胞中DNA损伤的诱导有关。GTPs诱导的I类HDAC蛋白水平降低是通过蛋白酶体降解介导的。HDAC抑制剂丙戊酸表现出类似的降低黑色素瘤细胞活力和诱导细胞死亡的模式。用GTPs处理A375和Hs294t细胞导致细胞周期G1期细胞周期蛋白和细胞周期蛋白依赖性激酶水平降低,而肿瘤抑制蛋白(Cip1/WAF1/p21、p16和p53)水平上调。