A role for dipeptidyl peptidase IV in suppressing the malignant phenotype of melanocytic cells Journal Article


Authors: Wesley, U. V.; Albino, A. P.; Tiwari, S.; Houghton, A. N.
Article Title: A role for dipeptidyl peptidase IV in suppressing the malignant phenotype of melanocytic cells
Abstract: Dipeptidyl peptidase IV (DPPIV) is a cell surface peptidase expressed by normal melanocytes, epithelial cells, and other cells. Malignant cells, including melanomas and carcinomas, frequently lose or alter DPPIV cell surface expression. Loss of DPPIV expression occurs during melanoma progression at a stage where transformed melanocytes become independent of exogenous growth factors for survival. Tetracycline-inducible expression vectors were constructed to express DPPIV in human melanoma cells. Reexpressing DPPIV in melanoma cells at or below levels expressed by normal melanocytes induced a profound change in phenotype that was characteristic of normal melanocytes. DPPIV expression led to a loss of tumorigenicity, anchorage-independent growth, a reversal in a block in differentiation, and an acquired dependence on exogenous growth factors for cell survival. Suppression of tumorigenicity and reversal of a block in differentiation were dependent on serine protease activity, assessed using mutant DPPIV molecules containing serine→alanine substitutions. Surprisingly, dependence on exogenous growth factors was not dependent on serine protease activity. Reexpression of either wild-type or mutant DPPIV rescued expression of a second putative cell surface serine peptidase, fibroblast activation protein α, which can form a heterodimer with DPPIV. This observation suggests that rescue of fibroblast activation protein α may play a role in regulating growth of melanocytic cells. These results support the view that downregulation of DPPIV is an important early event in the pathogenesis of melanoma.
Keywords: protein expression; human cell; phenotype; cell survival; cell cycle; cell division; melanoma; apoptosis; melanocyte; melanocytes; serine; membrane proteins; cell differentiation; tumor cells, cultured; enzyme activity; serine proteinase; serine endopeptidases; carcinogenicity; alanine; malignant transformation; anchorage independent growth; immunosuppressive agents; differentiation; culture media, conditioned; growth inhibitors; gelatinases; dipeptidyl peptidase iv; tumorigenicity; serine protease; humans; human; priority journal; article; antigens, cd26; fibroblast activating protein α
Journal Title: Journal of Experimental Medicine
Volume: 190
Issue: 3
ISSN: 0022-1007
Publisher: Rockefeller University Press  
Date Published: 1999-08-02
Start Page: 311
End Page: 322
Language: English
DOI: 10.1084/jem.190.3.311
PUBMED: 10430620
PROVIDER: scopus
PMCID: PMC2195594
DOI/URL:
Notes: Source: Scopus
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  1. Umadevi Wesley
    7 Wesley
  2. Shakuntala Tiwari
    8 Tiwari
  3. Alan N Houghton
    364 Houghton
  4. Anthony P. Albino
    111 Albino