A new concept of tumor promotion by tumor necrosis factor-alpha, and cancer preventive agents (-)-epigallocatechin gallate and green tea--a review.

Cancer detection and prevention Pub Date : 2000-01-01
H Fujiki, M Suganuma, S Okabe, E Sueoka, K Suga, K Imai, K Nakachi
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Abstract

The study of tumor promotion in rodent carcinogenesis using chemical tumor promoters has revealed various tumor promotion pathways, such as the 12-O-tetradecanoylphorbol-13-acetate (TPA) pathway mediated through activation of protein kinase C, and the okadaic acid pathway mediated through inhibition of protein phosphatases 1 and 2A (PP-1 and PP-2A). We previously demonstrated that application of TPA and okadaic acid induced tumor necrosis factor-alpha (TNF-alpha) gene expression in mouse skin, but that tautomycin, which is an inhibitor of PP-1 and PP-2A and not a tumor promoter on mouse skin, did not. Moreover, we found that TNF-alpha stimulated transformation of BALB/3T3 cells initiated with 3-methylcholanthrene 1,000 times stronger than did TPA (Cancer Res. 53, 1982-1985, 1993). This evidence demonstrates a link between the okadaic acid pathway and the endogenous tumor promotion pathway of TNF-alpha. Recently we presented the first evidence that tumor promotion in TNF-alpha(-/-) mice was significantly depressed compared with TNF-alpha(+/+) mice. Thus, in human carcinogenesis, we think that TNF-alpha and other inflammatory cytokines in preneoplastic lesion stimulate tumor promotion and progression of initiated cells as well as premalignant cells. The first part of this paper reports on this TNF-alpha tumor promotion pathway. In the second part, we report a promising screening method for cancer preventive agents, based on evidence that pretreatment with agents such as tamoxifen, sulindac, 1alpha, 25-(OH)2 vitamin D3, quercetin, caffeic acid phenethyl ester, and (-)-epigallocatechin gallate (EGCG) commonly inhibited TNF-alpha release from BALB/3T3 cells induced by okadaic acid. EGCG, the main constituent of Japanese green tea, and green tea itself are acknowledged cancer preventives in Japan, and this paper presents evidence of their effectiveness in both a high-risk group and the general population.

肿瘤坏死因子- α和抗癌药物(-)-表没食子儿茶素没食子酸酯和绿茶促进肿瘤的新概念综述。
利用化学肿瘤启动子研究啮齿动物癌变的肿瘤促进作用,揭示了多种肿瘤促进途径,如通过激活蛋白激酶C介导的12- o -十四烷醇-13-乙酸酯(TPA)途径,以及通过抑制蛋白磷酸酶1和2A (PP-1和PP-2A)介导的冈田酸途径。我们之前证明,TPA和冈田酸的应用诱导小鼠皮肤中肿瘤坏死因子- α (tnf - α)基因的表达,但他霉素(PP-1和PP-2A的抑制剂,而不是小鼠皮肤上的肿瘤启动子)没有。此外,我们发现tnf - α对3-甲基胆蒽诱导的BALB/3T3细胞转化的刺激比TPA强1000倍(Cancer Res. 53, 1982-1985, 1993)。这一证据表明冈田酸途径与内源性tnf - α促肿瘤途径之间存在联系。最近,我们首次提出证据表明,与tnf - α(+/+)小鼠相比,tnf - α(-/-)小鼠的肿瘤促进作用明显受到抑制。因此,在人类癌变中,我们认为肿瘤前病变中的tnf - α和其他炎性细胞因子刺激了起始细胞和癌前细胞的肿瘤促进和进展。本文第一部分报道了tnf - α促进肿瘤的途径。在第二部分,我们报道了一种很有前景的癌症预防药物筛选方法,基于有证据表明,预处理药物如他莫昔芬、舒林酸、1 α、25-(OH)2维生素D3、槲皮素、咖啡酸苯乙酯和(-)-表没食子儿茶素没食子酸酯(EGCG)通常可以抑制冈酸诱导的BALB/3T3细胞中tnf - α的释放。日本绿茶的主要成分EGCG和绿茶本身在日本都是公认的癌症预防物质,本文提出了它们在高危人群和普通人群中都有效的证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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