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α-MSH tripeptide analogs activate the melanocortin 1 receptor and reduce UV-induced DNA damage in human melanocytes

  • Published:2009-10 Issue:5 Volume:22 Page:635-644
  • ISSN:1755-1471
  • Container-title:Pigment Cell & Melanoma Research
  • language:en
  • Short-container-title:

Author:

Abdel-Malek Zalfa A.,Ruwe Andrew,Kavanagh-Starner Renny,Kadekaro Ana Luisa,Swope Viki,Haskell-Luevano Carrie,Koikov Leonid,Knittel James J.

Publisher

Wiley

Subject

Dermatology,General Biochemistry, Genetics and Molecular Biology,Oncology

Reference53 articles.

1. Mitogenic and melanogenic stimulation of normal human melanocytes by melanotropic peptides;Abdel-Malek;Proc. Natl. Acad. Sci. U.S.A.,1995

2. Melanoma prevention strategy based on using tetrapeptide alpha-MSH analogs that protect human melanocytes from UV-induced damage and cytotoxicity;Abdel-Malek;FASEB J.,2006

3. Absorption of peptide and peptidomimetic drugs;Amidon;Annu. Rev. Pharmacol. Toxicol.,1994

4. Inhibition of UV-induced p53 mutations by sunscreens: implications for skin cancer prevention;Ananthaswamy;J. Investig. Dermatol. Symp. Proc.,1998

5. Oligonucleotide treatment increases eumelanogenesis, hair pigmentation and melanocortin-1 receptor expression in the hair follicle;Atoyan;Exp. Dermatol.,2007

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