Mutational analysis of Chk1, Chk2, Apaf1 and Rb1 in human malignant melanoma cell lines

Thilo Papp*, Annett Niemetz, Nils Dosdahl, Krishan Kumar, Dietmar Schiffmann

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Four tumour suppressor genes (Chk1, Chk2, Apaf1 and Rb1) in nine human malignant melanoma cell lines were screened for a loss of gene expression, point mutations and small deletions/insertions by cDNA-based DGGE/SCCP analysis. In two cell lines alterations of the investigated genes could be demonstrated. This result confirms our assumption of the participation of dysfunctional p53 inducer/effector genes in human melanoma aetiology. Furthermore, it points towards the probable principal role of diverse alternative p53-pathway disruption mechanisms in this highly therapy-resistant malignancy without affecting p53 itself. To our knowledge, this is the first CHK1/CHK2 mutation screening in human melanoma.

Original languageEnglish (US)
Pages (from-to)135-140
Number of pages6
JournalOncology reports
Volume17
Issue number1
DOIs
StatePublished - Jan 2007

Keywords

  • Apaf1
  • Chk1
  • Chk2
  • DGGE
  • Human malignant melanoma
  • Rb1
  • SSCP

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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