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Polymeric black tea polyphenols inhibit mouse skin chemical carcinogenesis by decreasing cell proliferation

机译:聚合红茶多酚通过减少细胞增殖来抑制小鼠皮肤化学致癌作用

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摘要

: The aim of this study was to investigate the antitumour promoting effects and possible mechanisms of action of the most abundant polymeric black tea polyphenols (PBPs 1–5) or thearubigins, . : Effect of PBP pre‐treatments on 12‐ ‐tetradecanoylphorbol‐13‐acetate (TPA) promoted skin papillomas was studied in 7,12‐dimethylbenz(a)anthracene initiated mice over 40 weeks. Cell proliferation and apoptosis, in epidermis of the skin, were measured using appropriate immunohistochemical staining. Mitogen‐activated protein kinase signalling studies were conducted with Western blot analysis at 10, 20, 30 and 40 weeks of promotion. : Pre‐treatments with PBP fractions differentially altered latency, multiplicity and incidence of skin papillomas as compared to TPA treatments thereby exhibiting antipromoting effects. Most PBP fractions decreased TPA‐induced cell proliferation by decreasing activation of signalling kinases (c‐Jun N‐terminal protein kinase, extracellular signal‐regulated protein kinase, p38 protein kinase and Akt), transcription factors (activator protein‐1 and nuclear factor kappa B) and inflammatory protein (cyclooxygenase 2). TPA‐induced epidermal cell apoptosis was also decreased by pre‐treatment with most PBP fractions. Higher levels of p53 and p21 in skin cells pre‐treated with PBP fractions followed by TPA treatment as compared to only TPA‐treated animals suggested possible activation of a cell cycle checkpoint. : PBP‐2 was observed to be the most potent polymeric polyphenol fraction and PBP‐4 and PBP‐5 showed only marginal activity, whereas PBP‐1 and PBP‐3 displayed intermediate efficacies. In conclusion, the protective effects of PBP fractions could be attributed to inhibition of TPA‐induced cellular proliferation.
机译::这项研究的目的是研究最丰富的聚合红茶多酚(PBPs 1-5)或茶红素的抗肿瘤促进作用和可能的作用机理。在40周内,在7,12-二甲基苯并(a)蒽引发的小鼠中研究了PBP预处理对12-十四烷酰phorbol-13-乙酸盐(TPA)促进的皮肤乳头状瘤的影响。使用适当的免疫组织化学染色测量皮肤表皮中的细胞增殖和凋亡。在促进的10、20、30和40周使用Western blot分析进行了丝裂原活化的蛋白激酶信号转导研究。与TPA治疗相比,PBP分数的预处理差异性地改变了皮肤乳头状瘤的潜伏期,多样性和发生率,从而表现出抗促进作用。大多数PBP组分通过减少信号传导激酶(c-Jun N-末端蛋白激酶,细胞外信号调节蛋白激酶,p38蛋白激酶和Akt),转录因子(激活蛋白-1和核因子kappa)的激活来降低TPA诱导的细胞增殖B)和炎性蛋白质(环氧合酶2)。通过大多数PBP组分的预处理,TPA诱导的表皮细胞凋亡也减少了。与仅用TPA处理的动物相比,用PBP组分预处理并经TPA处理的皮肤细胞中较高的p53和p21水平提示可能激活了细胞周期检查点。 :观察到PBP-2是最有效的聚合物多酚馏分,PBP-4和PBP-5仅显示边缘活性,而PBP-1和PBP-3显示中等效力。总之,PBP组分的保护作用可能归因于TPA诱导的细胞增殖的抑制。

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