Acute and long-term cytogenetic effects of treatment in childhood cancer: sister-chromatid exchanges and chromosome aberrations

Mutat Res. 1982 Feb 22;92(1-2):291-307. doi: 10.1016/0027-5107(82)90232-9.

Abstract

The incidence of chromosomal aberrations in banded karyotypes and of sister-chromatid exchanges (SCEs) was determined in the lymphocytes of survivors of childhood cancer as 2 parameters which are pertinent in assessing the genetic damage induced by chemotherapy. The proportion of cells with chromosome breakage or structural rearrangement-type aberration was 1 cell in 67 in a control group of 8 untreated cancer patients and 2 parents of cancer patients, 1 cell in 8 in 12 patients currently on therapy, and 1 cell in 50 in 17 patients sampled 6 months to 35 years post-treatment. The range of mean SCE levels per cell was 4.5-6.5 in the untreated cancer patients, 4.0-9.6 in non-cancer controls, 3.3-33.7 in patients on therapy, and 4.6-9.7 in post-therapy survivors. Considerably variability was observed between individuals with both SCE and breakage assays but therapy-induced increases in SCEs were not necessarily correlated with increased levels of aberrations arising from chromosomal breakage.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Cells, Cultured
  • Child
  • Child, Preschool
  • Chromosome Aberrations*
  • Chromosome Banding
  • Crossing Over, Genetic*
  • Female
  • Follow-Up Studies
  • Humans
  • Infant
  • Lymphocytes / ultrastructure*
  • Male
  • Neoplasms / genetics
  • Neoplasms / therapy*
  • Sister Chromatid Exchange*