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Zinc alpha-2-glycoprotein regulates melanin production by normal and malignant melanocytes.

Publication ,  Journal Article
Hale, LP
Published in: J Invest Dermatol
August 2002

Zinc alpha-2-glycoprotein is secreted by a variety of normal and malignant epithelial cells and overexpression by tumors has been implicated in cancer cachexia. To investigate biologic properties of zinc alpha-2-glycoprotein further, stable transfectants of recombinant human zinc alpha-2-glycoprotein were created in the B16F10 murine melanoma cell line. Both B16-recombinant human zinc alpha-2-glycoprotein clones with strong expression of zinc alpha-2-glycoprotein and vector-transfected B16 cells treated with exogenous zinc alpha-2-glycoprotein had decreased melanin production in vitro. Furthermore, B16-recombinant human zinc alpha-2-glycoprotein clones formed amelanotic tumors in vivo, despite their melanin production in vitro. Although no qualitative differences in tyrosinase mRNA expression could be detected by reverse transcription-polymerase chain reaction, B16-recombinant human zinc alpha-2-glycoprotein tumors had decreased levels of tyrosinase protein and minimal tyrosinase activity. Purified zinc alpha-2-glycoprotein also decreased tyrosinase activity in vector-transfected B16 tumor sections in vitro. Taken together, these studies demonstrate that zinc alpha-2-glycoprotein inhibits melanin production by B16 melanoma cells via post-transcriptional effects on tyrosinase protein. As zinc alpha-2-glycoprotein decreases melanin synthesis more strongly in vivo than in vitro, however, it is likely that zinc alpha-2-glycoprotein affects melanin synthesis through indirect mechanisms as well. Zinc alpha-2-glycoprotein also inhibits melanin production by melan-A primary melanocytes in vitro. As zinc alpha-2-glycoprotein is normally produced by epidermal keratinocytes, these studies raise the possibility that epidermal-derived zinc alpha-2-glycoprotein may play a part in normal regulation of melanin production in vivo, in addition to its previously described role in cancer cachexia.

Duke Scholars

Published In

J Invest Dermatol

DOI

ISSN

0022-202X

Publication Date

August 2002

Volume

119

Issue

2

Start / End Page

464 / 470

Location

United States

Related Subject Headings

  • Zn-Alpha-2-Glycoprotein
  • Tumor Necrosis Factor-alpha
  • Seminal Plasma Proteins
  • Monophenol Monooxygenase
  • Mice
  • Melanoma, Experimental
  • Melanocytes
  • Melanins
  • Dermatology & Venereal Diseases
  • Cell Line
 

Citation

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Chicago
ICMJE
MLA
NLM
Hale, L. P. (2002). Zinc alpha-2-glycoprotein regulates melanin production by normal and malignant melanocytes. J Invest Dermatol, 119(2), 464–470. https://doi.org/10.1046/j.1523-1747.2002.01813.x
Hale, Laura P. “Zinc alpha-2-glycoprotein regulates melanin production by normal and malignant melanocytes.J Invest Dermatol 119, no. 2 (August 2002): 464–70. https://doi.org/10.1046/j.1523-1747.2002.01813.x.
Hale, Laura P. “Zinc alpha-2-glycoprotein regulates melanin production by normal and malignant melanocytes.J Invest Dermatol, vol. 119, no. 2, Aug. 2002, pp. 464–70. Pubmed, doi:10.1046/j.1523-1747.2002.01813.x.
Journal cover image

Published In

J Invest Dermatol

DOI

ISSN

0022-202X

Publication Date

August 2002

Volume

119

Issue

2

Start / End Page

464 / 470

Location

United States

Related Subject Headings

  • Zn-Alpha-2-Glycoprotein
  • Tumor Necrosis Factor-alpha
  • Seminal Plasma Proteins
  • Monophenol Monooxygenase
  • Mice
  • Melanoma, Experimental
  • Melanocytes
  • Melanins
  • Dermatology & Venereal Diseases
  • Cell Line