Noonan Douglas M, Benelli Roberto, Albini Adriana
Dipartimento di Scienze Biologiche e Cliniche, Università dell'Insubria, Varese, Italy.
Recent Results Cancer Res. 2007;174:219-24. doi: 10.1007/978-3-540-37696-5_19.
Angiogenesis is necessary for solid tumor growth and dissemination. In addition to angiogenesis, it has become increasingly clear that inflammation is a key component in cancer insurgence that can promote tumor angiogenesis. We noted that angiogenesis is a common and key target of most chemopreventive molecules, where they most likely suppress the angiogenic switch in premalignant tumors, a concept we termed angioprevention. We have shown that various molecules, such as flavonoids, antioxidants, and retinoids, act in the tumor microenvironment, inhibiting the recruitment and/or activation of endothelial cells and phagocytes of the innate immunity. N-acetyl-cysteine, and the green tea flavonoid epigallocatechin-3-gallate (EGCG) and the beer/ hops-derived chalcone Xanthohumol all prevent angiogenesis in the Matrigel sponge angiogenic assay in vivo and inhibit the growth of the highly angiogenic Kaposi's sarcoma tumor cells (KS-Imm) in nude mice. The synthetic retinoid 4-hydroxyfenretinide (4HPR) also shows anti-angiogenic effects. We analyzed the regulation of gene expression they exert in primary human umbilical endothelial cells (HUVEC) in culture with functional genomics. Expression profiles obtained through Affymetrix GeneChip arrays identified overlapping sets of genes regulated by anti-oxidants. In contrast, the ROS-producing 4HPR induced members of the TGFbeta-ligand superfamily, which, at least in part, explains its anti-angiogenic activity. NAC and the flavonoids all suppressed the IkB/NF-kappaB signaling pathway even in the presence of NF-kappaB stimulation by TNFalpha, and showed reduced expression of many NF-kappaB target genes. A selective apoptotic effect on transformed cells, but not on endothelial cells, of the anti-oxidants may be related to the reduced expression of the NF-kappaB-dependent survival factors Bcl2 and Birc5/surviving, which are selectively overexpressed in transformed cells by these factors. The repression of the NF-kappaB pathway suggests anti-inflammatory effects for the antioxidant compounds that may also represent an indirect role in angiogenesis inhibition. The green tea flavonoid EGCG does target inflammatory cells, mostly neutrophils, and inhibits inflammation-associated angiogenesis. The other angiopreventive molecules are turning out to be effective modulators of phagocyte recruitment and activation, further linking inflammation and vascularization to tumor onset and progression and providing a key target for cancer prevention.
血管生成是实体瘤生长和扩散所必需的。除血管生成外,越来越清楚的是,炎症是癌症发生的关键组成部分,可促进肿瘤血管生成。我们注意到血管生成是大多数化学预防分子的共同且关键的靶点,它们很可能抑制癌前肿瘤中的血管生成开关,我们将这一概念称为血管预防。我们已经表明,各种分子,如类黄酮、抗氧化剂和视黄酸,在肿瘤微环境中发挥作用,抑制先天免疫的内皮细胞和吞噬细胞的募集和/或激活。N-乙酰半胱氨酸、绿茶类黄酮表没食子儿茶素-3-没食子酸酯(EGCG)以及啤酒/啤酒花衍生的查耳酮黄腐酚,在体内基质胶海绵血管生成试验中均能预防血管生成,并抑制裸鼠中高血管生成性卡波西肉瘤肿瘤细胞(KS-Imm)的生长。合成视黄酸4-羟基芬维A胺(4HPR)也显示出抗血管生成作用。我们用功能基因组学分析了它们在培养的原代人脐静脉内皮细胞(HUVEC)中对基因表达的调控。通过Affymetrix基因芯片阵列获得的表达谱鉴定出了由抗氧化剂调控的重叠基因集。相比之下,产生ROS的4HPR诱导了TGFβ配体超家族的成员,这至少部分解释了其抗血管生成活性。NAC和类黄酮即使在存在TNFα刺激NF-κB的情况下,也均抑制IkB/NF-κB信号通路,并使许多NF-κB靶基因的表达降低。抗氧化剂对转化细胞而非内皮细胞的选择性凋亡作用,可能与NF-κB依赖性存活因子Bcl2和Birc5/存活蛋白的表达降低有关,这些因子在转化细胞中被这些因子选择性过表达。NF-κB途径的抑制表明抗氧化剂化合物具有抗炎作用,这也可能在血管生成抑制中发挥间接作用。绿茶类黄酮EGCG确实作用于炎症细胞,主要是中性粒细胞,并抑制与炎症相关的血管生成。其他血管预防分子正被证明是吞噬细胞募集和激活的有效调节剂,进一步将炎症和血管化与肿瘤的发生和发展联系起来,并为癌症预防提供了一个关键靶点。