Biology of melanogenesis and the search for hypopigmenting agents
Increased production and accumulation of melanin are characteristics of a large number of skin diseases, including melasma, post-inflammatory hyperpigmentation and lentigo. A number of clinical agents can reduce normal or abnormal pigmentation, but none of these have achieved satisfactory effects. T...
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doaj-9d614408db224691a34e1bd828e15cdc2020-11-25T01:11:13ZengWolters Kluwer Medknow PublicationsDermatologica Sinica1027-81172010-06-01282535810.1016/S1027-8117(10)60011-0Biology of melanogenesis and the search for hypopigmenting agentsKyoung-Chan Park0Sun Young Huh1Hye Ryung Choi2Dong-Seok Kim3Department of Dermatology, Seoul National University College of Medicine, Seoul, KoreaDepartment of Dermatology, Seoul National University College of Medicine, Seoul, KoreaDepartment of Dermatology, Seoul National University College of Medicine, Seoul, KoreaDepartment of Biochemistry, College of Medicine, Chung-Ang University, Seoul, KoreaIncreased production and accumulation of melanin are characteristics of a large number of skin diseases, including melasma, post-inflammatory hyperpigmentation and lentigo. A number of clinical agents can reduce normal or abnormal pigmentation, but none of these have achieved satisfactory effects. This review discusses the mechanisms behind the different approaches. Tyrosinase is a pivotal enzyme in melanin synthesis. The majority of whitening or lightening agents act by specifically reducing the activity of tyrosinase via several mechanisms: (1) prior to melanin synthesis (interfering with its transcription and/or glycosylation); (2) during melanin synthesis (tyrosinase inhibition, peroxidase inhibition and reduction of byproducts); and (3) after melanin synthesis (tyrosinase degradation, inhibition of melanosome transfer, acceleration of skin turnover). Additional melanogenesis-associated mechanisms are also discussed.http://www.sciencedirect.com/science/article/pii/S1027811710600110MechanismMelaninTyrosinase |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kyoung-Chan Park Sun Young Huh Hye Ryung Choi Dong-Seok Kim |
spellingShingle |
Kyoung-Chan Park Sun Young Huh Hye Ryung Choi Dong-Seok Kim Biology of melanogenesis and the search for hypopigmenting agents Dermatologica Sinica Mechanism Melanin Tyrosinase |
author_facet |
Kyoung-Chan Park Sun Young Huh Hye Ryung Choi Dong-Seok Kim |
author_sort |
Kyoung-Chan Park |
title |
Biology of melanogenesis and the search for hypopigmenting agents |
title_short |
Biology of melanogenesis and the search for hypopigmenting agents |
title_full |
Biology of melanogenesis and the search for hypopigmenting agents |
title_fullStr |
Biology of melanogenesis and the search for hypopigmenting agents |
title_full_unstemmed |
Biology of melanogenesis and the search for hypopigmenting agents |
title_sort |
biology of melanogenesis and the search for hypopigmenting agents |
publisher |
Wolters Kluwer Medknow Publications |
series |
Dermatologica Sinica |
issn |
1027-8117 |
publishDate |
2010-06-01 |
description |
Increased production and accumulation of melanin are characteristics of a large number of skin diseases, including melasma, post-inflammatory hyperpigmentation and lentigo. A number of clinical agents can reduce normal or abnormal pigmentation, but none of these have achieved satisfactory effects. This review discusses the mechanisms behind the different approaches. Tyrosinase is a pivotal enzyme in melanin synthesis. The majority of whitening or lightening agents act by specifically reducing the activity of tyrosinase via several mechanisms: (1) prior to melanin synthesis (interfering with its transcription and/or glycosylation); (2) during melanin synthesis (tyrosinase inhibition, peroxidase inhibition and reduction of byproducts); and (3) after melanin synthesis (tyrosinase degradation, inhibition of melanosome transfer, acceleration of skin turnover). Additional melanogenesis-associated mechanisms are also discussed. |
topic |
Mechanism Melanin Tyrosinase |
url |
http://www.sciencedirect.com/science/article/pii/S1027811710600110 |
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