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Pre-clinical evidences for the efficacy of tryptanthrin as a potent suppressor of skin cancer.
Tryp菊酯作为皮肤癌有效抑制因子疗效的临床前证据。
- 影响因子:4.39
- DOI:10.1111/cpr.12710
- 作者列表:"Shankar G M","Alex VV","Nisthul A A","Bava SV","Sundaram S","Retnakumari AP","Chittalakkottu S","Anto RJ
- 发表时间:2020-01-01
Abstract
OBJECTIVE:Clinical trials have demonstrated the efficacy of indigo naturalis, a traditional Chinese medicine ingredient, against psoriasis, a skin disease characterized by keratinocyte hyperproliferation and inflammation. The present study investigates the efficacy of tryptanthrin, a bioactive compound in indigo naturalis, against non-melanoma skin cancer (NMSC) and the signalling events involved. METHODS:Efficacy of tryptanthrin against NMSC was assessed using DMBA/PMA-induced skin carcinogenesis model in Swiss albino mice. Immunostaining for PCNA and ki-67 was used to mark proliferating cells in tissues. Haematoxylin and eosin staining and toluidine staining were employed to assess inflammation, and TUNEL assay was used to detect apoptosis in tissues. The signalling events were evaluated using Western blot, imunohistochemistry and immunofluorescence staining. MTT assay and clonogenic assay were performed to assess the viability and proliferation of cancer cells, in vitro. RESULTS:In mice, topical application of tryptanthrin suppressed skin carcinogenesis. It attenuated inflammation, impeded the proliferation of hair follicle (HF) cells and suppressed the activation of β-catenin, a major driver of HF cell proliferation. Additionally tryptanthrin suppressed the activation of ERK1/2 and p38, both of which promote β-catenin activation and lowered the expression of c-Myc and cyclin-D1. Tryptanthrin suppressed the proliferation of the human NMSC cell line, A431 and abrogated EGF-induced activation of β-catenin and subsequent cytoskeletal rearrangement. CONCLUSION:The study demonstrates with molecular evidence that tryptanthrin is an effective suppressor of NMSC.
摘要
目的: 临床试验证明了中药成分青黛对以角质形成细胞过度增殖和炎症为特征的皮肤病银屑病的疗效。本研究调查了青黛中的生物活性化合物tryp菊酯对非黑色素瘤皮肤癌 (NMSC) 的疗效和所涉及的信号事件。 方法: 采用DMBA/PMA诱导的瑞士白化小鼠皮肤癌变模型,评估tryp菊酯对NMSC的疗效。用PCNA和ki-67 免疫染色标记组织中增殖细胞。采用苏木精伊红染色和甲苯胺染色评估炎症,TUNEL法检测组织细胞凋亡。使用Western blot、免疫组织化学和免疫荧光染色评价信号事件。MTT实验和克隆形成实验在体外评估癌细胞的活力和增殖。 结果: 在小鼠中,局部应用tryp菊酯可抑制皮肤癌变。它减轻了炎症,阻碍了毛囊 (HF) 细胞的增殖,抑制了HF细胞增殖的主要驱动因子 β-catenin的活化。此外,tryp菊酯抑制ERK1/2 和p38 的活化,两者均促进 β-catenin的活化,降低c-Myc和cyclin-D1 的表达。Tryp菊酯抑制人NMSC细胞系A431 的增殖,并消除EGF诱导的 β-catenin活化和随后的细胞骨架重排。 结论: 有分子证据表明tryp菊酯是NMSC的有效抑制因子。
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皮肤肿瘤是发生在皮肤的细胞增生性疾病,是一种常见病。发生于皮内或皮下组织的新生物,种类很多,临床上分良性肿瘤和恶性肿瘤。恶性肿瘤可以不断增殖,引起转移,威胁生命,称为皮肤癌。