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Evaluation of pentacyclic triterpenes found in Perilla frutescens for inhibition of skin tumor promotion by 12-O-tetradecanoylphorbol-13-acetate

机译:评价紫苏中发现的五环三萜类化合物对12-O-十四烷酰佛波醇13-乙酸盐抑制皮肤肿瘤的促进作用

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摘要

A series of pentacyclic tritperpenes found in Perilla frutescens (P. frutescens), including ursolic acid (UA), oleanolic acid (OA), corosolic acid (CA), 3-epi-corosolic acid (3-epiCA), maslinic acid (MA), and 3-epi-maslinic acid (3-epiMA) were evaluated for their effects on epidermal cell signaling, proliferation, and skin inflammation in relation to their ability to inhibit skin tumor promotion by 12-O-tetradecanoylphorbol-13-acetate (TPA) and compared to UA as the prototype compound. All compounds were given topically 30 min prior to each TPA application and significantly inhibited skin tumor promotion. 3-epiCA and MA were significantly more effective than UA at inhibiting tumor development. All of these compounds significantly inhibited epidermal proliferation induced by TPA, however, CA, 3-epiCA and MA were more effective than UA. All compounds also reduced skin inflammation (assessed by infiltration of mast cells and T-cells) and inflammatory gene expression induced by TPA, however, 3-epiCA and MA were again more effective than UA. The greater ability of 3-epiCA and MA to inhibit skin tumor promotion was associated with greater reduction of Cox-2 and Twist1 proteins and inhibition of activation (i.e., phosphorylation) of IGF-1R, STAT3 and Src. Further study of these compounds, especially 3-epiCA and MA, for chemopreventive activity in other cancer model systems is warranted.
机译:紫苏(P. frutescens)中发现的一系列五环三萜烯,包括熊果酸(UA),齐墩果酸(OA),熊果酸(CA),3-表叶果酸(3-epiCA),马来酸(MA) )和3-表山梨酸(3-epiMA)对表皮细胞信号传导,增殖和皮肤炎症的影响,以及它们通过12-O-十四烷酰phorbol-13-乙酸盐抑制皮肤肿瘤生长的能力( TPA),并与UA作原型化合物进行比较。在每次TPA施用前30分钟局部给予所有化合物,并显着抑制皮肤肿瘤的生长。 3-epiCA和MA在抑制肿瘤发生方面比UA更为有效。所有这些化合物均显着抑制TPA诱导的表皮增殖,但是,CA,3-epiCA和MA比UA更有效。所有化合物还减少了皮肤炎症(通过肥大细胞和T细胞浸润评估)和TPA诱导的炎症基因表达,但是,3-epiCA和MA再次比UA更有效。 3-epiCA和MA抑制皮肤肿瘤生长的能力增强与Cox-2和Twist1蛋白的降低程度更大以及IGF-1R,STAT3和Src的激活(即磷酸化)受到抑制有关。这些化合物,尤其是3-epiCA和MA,需要进一步研究其在其他癌症模型系统中的化学预防活性。

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