Regulation of angiogenesis and inflammatory pathways by glycyrrhizic acid

Doaa D. Mohamed, H. Mahrous, Hany Khalil, Ibrahim A. Ibrahim, Dalia D. Mohamed, Omar S. Keshk, Alaa H. Nada, A. I. Maksoud
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Abstract

Skin cancer accounts for most malignancies across the globe. They are primarily divided into melanoma and nonmelanoma skin malignancies. Nonmelanoma skin cancer includes basal cell carcinoma and squamous cell carcinoma. Glycyrrhetinic acid (GA) is a bioactive compound extracted from licorice that exhibits an inhibition effect on various cancers. GA has been reported to have in vitro cytotoxic effects on several human cancer cells. However, reports on the mode of action and detailed mechanism of GA in vitro in skin cancer disease are limited. Hence, GA’s effect on the human skin cell line BJ and MCC13 was investigated. MTT assay showed that GA had cytotoxic effects on MCC13 cells but was non-toxic to the normal cells of BJ in a time-dose dependent manner. GA also inhibited the angiogenic sprouting of new blood vessels in tumor progression. In gene expression assay, GA induces mitochondrial apoptosis through the induction and inhibition of Cytochrome C and Bcl2 respectively. In conclusion, GA is a potent candidate to induce apoptosis and concurrently inhibit the invasion, migration, and angiogenesis of the MCC13 cell line through increasing TNF-alpha concentration resulting in the necroptotic pathway induction.
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甘草酸调节血管生成和炎症途径
皮肤癌占全球恶性肿瘤的大多数。它们主要分为黑色素瘤和非黑色素瘤皮肤恶性肿瘤。非黑色素瘤皮肤癌包括基底细胞癌和鳞状细胞癌。甘草次酸(GA)是从甘草中提取的一种生物活性化合物,对多种癌症有抑制作用。据报道,GA 对几种人类癌细胞具有体外细胞毒性作用。然而,有关 GA 在体外对皮肤癌疾病的作用模式和详细机制的报道却很有限。因此,我们研究了 GA 对人类皮肤细胞系 BJ 和 MCC13 的影响。MTT 分析表明,GA 对 MCC13 细胞有细胞毒性作用,但对 BJ 的正常细胞无毒性,且有时间剂量依赖性。GA 还能抑制肿瘤生长过程中新生血管的萌发。在基因表达检测中,GA分别通过诱导和抑制细胞色素C和Bcl2诱导线粒体凋亡。总之,GA 是一种有效的候选物质,可通过增加 TNF-α 浓度导致坏死通路诱导 MCC13 细胞株凋亡,并同时抑制其侵袭、迁移和血管生成。
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