A cell line from Wilms' tumour with deletion in short arm of chromosome II

Int J Cancer. 1987 Oct 15;40(4):499-504. doi: 10.1002/ijc.2910400412.

Abstract

A cell line (T3/73) from a Wilms' tumour has been established from a 9 month-old boy with aniridia. The tumour was removed in 1973. On histological examination a diagnosis of Wilms' tumour was made which showed undifferentiated areas, marked tubule formation and abundant striped muscle fibres. The tumour cells, which are fusiform, grew rapidly in culture without the addition of growth factors, and have undergone over 100 passages. Approximately 95% and 5% were positive for desmin and cytokeratin, respectively. The cell doubling time was 28 hr. Cytogenetic studies revealed a karyotype of 46,XY,del(11) (p12::p14). Although the cells stained very intensely with a monoclonal antibody that detects oncogene ras p 21 antigen, Southern blot analysis using c-Ha-ras as a probe failed to reveal an obvious deletion or amplification of either Ha-ras allele.

Publication types

  • Case Reports

MeSH terms

  • Antibodies, Monoclonal
  • Cell Line
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 11*
  • Desmin / analysis
  • Gene Amplification
  • Humans
  • Infant
  • Karyotyping
  • Keratins / analysis
  • Male
  • Oncogenes
  • Proto-Oncogene Proteins / analysis
  • Proto-Oncogene Proteins p21(ras)
  • Wilms Tumor / genetics*

Substances

  • Antibodies, Monoclonal
  • Desmin
  • Proto-Oncogene Proteins
  • Keratins
  • HRAS protein, human
  • Proto-Oncogene Proteins p21(ras)