Kim Byung-Hak, Park Kyoung Chan, Park Jeong Ho, Lee Chung Gi, Ye Sang-Kyu, Park Jung Youl
Department of Pharmacology, Seoul National University College of Medicine, Seoul, 03080, Republic of Korea; CYTUS H&B Co., Ltd, Cheongju, 28160, Republic of Korea.
Department of Chemical & Biological Engineering, Hanbat National University, Daejeon, 34158, Republic of Korea.
Biochem Biophys Res Commun. 2016 Nov 25;480(4):648-654. doi: 10.1016/j.bbrc.2016.10.110. Epub 2016 Oct 27.
Abnormal accumulation of melanin pigments in the skin can be lead to hyperpigmentation disorders and melanoma. Melanin biosynthesis is ultimately regulated by the rate-limiting enzyme tyrosinase. In the present study, we synthesized chalcone derivatives and identified 1-(2-cyclohexylmethoxy-6-hydroxy-phenyl)-3-(4-hydroxymethyl-phenyl)-propenone (chalcone-21) as an anti-melanogenic substance in B16F10 melanoma cells. Chalcone-21 strongly inhibited cellular melanin production and tyrosinase activity in B16F10 melanoma cells stimulated with α-melanocyte stimulating hormone (α-MSH) or protoporphyrin IX. In addition, the compound suppressed not only the expression of tyrosinase, tyrosinase-related protein-1 (TRP-1), TRP-2, and microphthalmia-associated transcription factor (MITF), but also the transcriptional activity of tyrosinase and MITF. Our results demonstrated chalcone-21 to be an effective depigmenting agent.
皮肤中黑色素的异常积累会导致色素沉着紊乱和黑色素瘤。黑色素的生物合成最终由限速酶酪氨酸酶调控。在本研究中,我们合成了查尔酮衍生物,并鉴定出1-(2-环己基甲氧基-6-羟基苯基)-3-(4-羟甲基苯基)-丙烯酮(查尔酮-21)是B16F10黑色素瘤细胞中的一种抗黑色素生成物质。查尔酮-21强烈抑制α-黑素细胞刺激素(α-MSH)或原卟啉IX刺激的B16F10黑色素瘤细胞中的细胞黑色素生成和酪氨酸酶活性。此外,该化合物不仅抑制酪氨酸酶、酪氨酸酶相关蛋白-1(TRP-1)、TRP-2和小眼相关转录因子(MITF)的表达,还抑制酪氨酸酶和MITF的转录活性。我们的结果表明查尔酮-21是一种有效的色素沉着减退剂。