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Bioscience, Biotechnology, and Biochemistry Volume 73, 2009 - Issue 6
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Original Articles

Effects of Theaflavins on Melanin Biosynthesis in Mouse B16 Melanoma Cells

Yuriko YAMAOKAAichikonan Junior College
,
Kenji OHGUCHIGifu International Institute of Biotechnology
,
Tomohiro ITOHGifu International Institute of Biotechnology
,
Yoshinori NOZAWAGifu International Institute of Biotechnology
&
Yukihiro AKAOGifu International Institute of Biotechnology
Pages 1429-1431 | Received 11 Dec 2008, Accepted 27 Feb 2009, Published online: 22 May 2014

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Ichiro SHIRASUGI, Yoichi SAKAKIBARA, Masao YAMASAKI, Kazuo NISHIYAMA, Takashi MATSUI, Ming-Cheh LIU & Masahito SUIKO. (2010) Novel Screening Method for Potential Skin-Whitening Compounds by a Luciferase Reporter Assay. Bioscience, Biotechnology, and Biochemistry 74:11, pages 2253-2258.
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Articles from other publishers (15)

Wei Wang, Taimei Di, Weiwei Wang & Heyuan Jiang. (2023) EGCG, GCG, TFDG, or TSA Inhibiting Melanin Synthesis by Downregulating MC1R Expression. International Journal of Molecular Sciences 24:13, pages 11017.
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Lingli Sun, Shuai Wen, Qiuhua Li, Xingfei Lai, Ruohong Chen, Zhenbiao Zhang, Junxi Cao & Shili Sun. (2022) Theaflavin-3,3′-di-gallate represses prostate cancer by activating the PKCδ/aSMase signaling pathway through a 67 kDa laminin receptor. Food & Function 13:8, pages 4421-4431.
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Peijun Zhao, Na Hyun Park, Md Badrul Alam & Sang-Han Lee. (2022) Fuzhuan Brick Tea Boosts Melanogenesis and Prevents Hair Graying through Reduction of Oxidative Stress via NRF2-HO-1 Signaling. Antioxidants 11:3, pages 599.
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Wei Wang, Lin Chen, Weiwei Wang, Jianyong Zhang, Ulrich H. Engelhardt & Heyuan Jiang. (2022) Effect of Active Groups and Oxidative Dimerization on the Antimelanogenic Activity of Catechins and Their Dimeric Oxidation Products. Journal of Agricultural and Food Chemistry 70:4, pages 1304-1315.
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Zhiguo Shan, Muhammad Farrukh Nisar, Mingxi Li, Chunhua Zhang & Chunpeng (Craig) Wan. (2021) Theaflavin Chemistry and Its Health Benefits. Oxidative Medicine and Cellular Longevity 2021, pages 1-16.
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Eric J. O’Neill, Deborah Termini, Alexandria Albano & Evangelia Tsiani. (2021) Anti-Cancer Properties of Theaflavins. Molecules 26:4, pages 987.
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Xiangna Zhang, Juan Li, Yinhua Li, Zhonghua Liu, Yong Lin & Jian-an Huang. (2020) Anti-melanogenic effects of epigallocatechin-3-gallate (EGCG), epicatechin-3-gallate (ECG) and gallocatechin-3-gallate (GCG) via down-regulation of cAMP/CREB /MITF signaling pathway in B16F10 melanoma cells. Fitoterapia 145, pages 104634.
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Phil June Park, Chan-Su Rha & Sung Tae Kim. (2019) Theaflavin-Enriched Fraction Stimulates Adipogenesis in Human Subcutaneous Fat Cells. International Journal of Molecular Sciences 20:8, pages 2034.
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Pulok K. Mukherjee, Rajarshi Biswas, Akanksha Sharma, Subhodip Banerjee, Sayan Biswas & C.K. Katiyar. (2018) Validation of medicinal herbs for anti-tyrosinase potential. Journal of Herbal Medicine 14, pages 1-16.
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Jung, Su-young, 심미옥 & 최인영. (2016) Whitening effect of black tea extracts of Ungpo Region, Korea. The Journal of Tea Culture & Industry Studies 34:null, pages 133-152.
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Kazuya Hagiwara, Masae Okura, Yasuyuki Sumikawa, Tokimasa Hida, Atsushi Kuno, Yoshiyuki Horio & Toshiharu Yamashita. (2016) Biochemical effects of the flavanol-rich lychee fruit extract on the melanin biosynthesis and reactive oxygen species. The Journal of Dermatology 43:10, pages 1174-1183.
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Young Chul KimSo Young ChoiEun Ye Park. (2015) Anti-melanogenic effects of black, green, and white tea extracts on immortalized melanocytes. Journal of Veterinary Science 16:2, pages 135.
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Te-Sheng Chang. (2012) Natural Melanogenesis Inhibitors Acting Through the Down-Regulation of Tyrosinase Activity. Materials 5:9, pages 1661-1685.
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Addanki P. Kumar, Heather Graham, Craig Robson, Karthik Garapati & Rita Ghosh. 2011. Evidence-based Anticancer Materia Medica. Evidence-based Anticancer Materia Medica 1 36 .
Minghui Bai, Jing Huang, Xiaolong Zheng, Zhibin Song, Miru Tang, Wuxiang Mao, Libo Yuan, Jun Wu, Xiaocheng Weng & Xiang Zhou. (2010) Highly Selective Suppression of Melanoma Cells by Inducible DNA Cross-Linking Agents: Bis(catechol) Derivatives. Journal of the American Chemical Society 132:43, pages 15321-15327.
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