Mutations and defective expression of the WAF1 p21 tumour-suppressor gene in malignant melanomas Journal Article


Authors: Vidal, M. J.; Loganzo, F. Jr; de Oliveira, A. R.; Hayward, N. K.; Albino, A. P.
Article Title: Mutations and defective expression of the WAF1 p21 tumour-suppressor gene in malignant melanomas
Abstract: The WAF1 gene, located on chromosome 6p, encodes a Mr 21 000 protein (p21) that can arrest cell growth by associating with and inhibiting cyclin-dependent kinase complexes that are necessary for cells to exit Gr. Transcriptional activation of WAF1 can be accomplished by increasing levels of p53 protein induced by various cellular stresses, including DNA damage. Metastatic melanomas are paradoxical in that most overexpress wild-type p53 protein, yet cell growth is not inhibited. Thus, it is possible that lack of growth suppression in melanomas is due, in part, to mutations in the WAF1 gene. Therefore, we examined the entire coding region of the WAF1 gene in 24 metastatic melanoma cell lines and three normal melanocyte lines by single-strand conformation polymorphism (SSCP) analysis and direct DNA sequencing. We similarly examined the DNA from lymphoblastoid cell lines, derived from nine individuals belonging to seven melanoma-prone families, in which haplotypes of markers on 6p co-segregate with melanoma for germline mutations in the WAF1 gene. Results indicate that (i) mutation of the WAF1 gene is an infrequent event in individuals with sporadic melanoma or predisposed to familial melanoma and (ii) the uncontrolled growth of melanoma cells is not due to mutation of the WAF1 gene. However, expression studies found a wide variation in the level of p21 protein in melanoma cells, suggesting that aberrant regulation of p21 may play a role in melanoma development. Moreover, there was no predictable relationship between p21 expression and p53 expression, indicating that other, p53-independent, pathways may be important for the regulation of p21 in melanoma cells. © 1995 Rapid Communications of Oxford Ltd.
Keywords: controlled study; gene mutation; human cell; mutation; comparative study; melanoma; gene expression; melanocyte; melanocytes; cell line; protein p53; tumor suppressor gene; rna, messenger; reference values; dna, neoplasm; cyclins; protein p21; lymphocytes; genes, tumor suppressor; polymorphism, single-stranded conformational; human; priority journal; article; support, non-u.s. gov't
Journal Title: Melanoma Research
Volume: 5
Issue: 4
ISSN: 0960-8931
Publisher: Lippincott Williams & Wilkins  
Date Published: 1995-08-01
Start Page: 243
End Page: 250
Language: English
DOI: 10.1097/00008390-199508000-00006
PUBMED: 7496159
PROVIDER: scopus
DOI/URL:
Notes: Source: Scopus
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  1. Anthony P. Albino
    111 Albino
  2. Frank Loganzo Jr
    15 Loganzo