An allelotype of papillary thyroid cancer

Int J Cancer. 1996 Dec 20;69(6):442-4. doi: 10.1002/(SICI)1097-0215(19961220)69:6<442::AID-IJC3>3.0.CO;2-4.

Abstract

Although papillary carcinoma accounts for approximately 70% of all thyroid cancers, preliminary studies of allelic loss have thus far not identified any areas of chromosomal deletion. We evaluated 30 papillary thyroid carcinomas for chromosomal loss/allelic imbalance by testing at least 2 microsatellite markers from every autosomal arm. Fifteen of the 30 tumors tested exhibited loss of heterozygosity/allelic imbalance (LOH/AI) at one or more loci. Chromosomal arms with frequent LOH/AI included 4q, 5p, 7p and 11p. An average of 1.1 chromosomal arms displayed LOH/AI in each individual tumor. Therefore, 4q, 5p, 7p and, to a lesser extent, 11p display significant LOH/AI in papillary thyroid cancer, which indicates the presence of putative tumor-suppressor gene loci at these chromosomal arms.

MeSH terms

  • Alleles*
  • Carcinoma, Papillary / genetics*
  • Carcinoma, Papillary / pathology
  • Chromosome Aberrations / genetics*
  • DNA, Neoplasm / isolation & purification
  • Heterozygote
  • Humans
  • Microsatellite Repeats / genetics
  • Polymerase Chain Reaction / methods
  • Thyroid Neoplasms / genetics*
  • Thyroid Neoplasms / pathology

Substances

  • DNA, Neoplasm