黄芩素通过p38丝裂原激活蛋白激酶途径抑制B16F10小鼠黑色素瘤细胞中α-刺激黑色素细胞激素刺激的黑色素生成

IF 2.5 Q3 ONCOLOGY Journal of Cancer Prevention Pub Date : 2023-06-30 DOI:10.15430/JCP.2023.28.2.40
Min Chang Oh, Pincha Devage Sameera Madushan Fernando, Mei Jing Piao, Kyoung Ah Kang, Herath Mudiyanselage Udari Lakmini Herath, Jin Won Hyun
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引用次数: 0

摘要

过量的UVB暴露通过α-促黑素细胞激素(α-MSH)的分泌导致恶性和非恶性黑色素瘤的发展。我们研究了黄芩素(5,6,7-三羟基黄酮)是否能抑制α- msh刺激的黑色素生成。黄芩素可以抑制UVB-和α- msh诱导的黑色素生成,减弱α- msh刺激的酪氨酸酶(单酚单加氧酶)活性,降低酪氨酸酶和酪氨酸相关蛋白-2的表达。此外,黄黄素通过p38丝裂原激活蛋白激酶信号通路阻止黑色素形成和色素沉着。这些发现表明黄芩素是一种天然的抑制黑色素生成的化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Baicalein Inhibits α-Melanocyte-stimulating Hormone-stimulated Melanogenesis via p38 Mitogen-activated Protein Kinase Pathway in B16F10 Mouse Melanoma Cells.

Excessive UVB exposure causes development of both malignant and non-malignant melanoma via the secretion of α-melanocyte-stimulating hormone (α-MSH). We investigated whether baicalein (5,6,7-trihydroxyflavone) could inhibit α-MSH-stimulated melanogenesis. Baicalein prevented UVB- and α-MSH-induced melanin production and attenuated α-MSH-stimulated tyrosinase (monophenol monooxygenase) activity, and expression of tyrosinase and tyrosine-related protein-2. In addition, baicalein prevented melanogenesis and pigmentation via the p38 mitogen-activated protein kinases signaling pathway. These findings suggest that baicalein represents a natural compound for attenuating melanogenesis.

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