Katiyar Santosh K
Department of Dermatology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Cancer Lett. 2007 Sep 18;255(1):1-11. doi: 10.1016/j.canlet.2007.02.010. Epub 2007 Mar 26.
Studies of immune-suppressed transplant recipients and patients with biopsy-proven skin cancer have confirmed that ultraviolet (UV) radiation-induced immune suppression is a risk factor for the development of skin cancer in humans. UV radiation suppresses the immune system in several ways. The UVB spectrum inhibits antigen presentation, induces the release of immunosuppressive cytokines, and elicits DNA damage that is a molecular trigger of UV-mediated immunosuppression. It is therefore important to elucidate the mechanisms underlying UV-induced immunosuppression as a basis for developing strategies to protect individuals from this effect and subsequent development of skin cancer. Dietary botanicals are of particular interest as they have been shown to inhibit UV-induced immune suppression and photocarcinogenesis. In this review, we summarize the most recent investigations and mechanistic studies regarding the photoprotective efficacy of selected dietary agents, including, green tea polyphenols, grape seed proanthocyanidins and silymarin. We present evidence that these chemopreventive agents prevent UVB-induced immunosuppression and photocarcinogenesis through: (i) the induction of immunoregulatory cytokine interleukin (IL)-12; (ii) IL-12-dependent DNA repair; and (iii) stimulation of cytotoxic T cells in the tumor microenvironment. The new information regarding the mechanisms of action of these agents supports their potential use as adjuncts in the prevention of photocarcinogenesis.
对免疫抑制的移植受者和经活检证实患有皮肤癌的患者的研究证实,紫外线(UV)辐射诱导的免疫抑制是人类患皮肤癌的一个风险因素。紫外线辐射通过多种方式抑制免疫系统。UVB光谱抑制抗原呈递,诱导免疫抑制细胞因子的释放,并引发DNA损伤,这是紫外线介导的免疫抑制的分子触发因素。因此,阐明紫外线诱导免疫抑制的潜在机制,对于制定保护个体免受这种影响及后续皮肤癌发生的策略至关重要。膳食植物成分尤其令人关注,因为它们已被证明能抑制紫外线诱导的免疫抑制和光致癌作用。在这篇综述中,我们总结了有关选定膳食成分(包括绿茶多酚、葡萄籽原花青素和水飞蓟宾)光保护功效的最新研究和机制研究。我们提供的证据表明,这些化学预防剂通过以下方式预防UVB诱导的免疫抑制和光致癌作用:(i)诱导免疫调节细胞因子白细胞介素(IL)-12;(ii)依赖IL-12的DNA修复;以及(iii)刺激肿瘤微环境中的细胞毒性T细胞。有关这些成分作用机制的新信息支持了它们作为预防光致癌作用辅助手段的潜在用途。