Deletion mapping of the tumor suppressor locus involved in colorectal cancer on chromosome band 8p21

Genes Chromosomes Cancer. 1999 Jun;25(2):147-53. doi: 10.1002/(sici)1098-2264(199906)25:2<147::aid-gcc10>3.0.co;2-z.

Abstract

Several somatic genetic alterations have been described in colorectal carcinoma (CRC). Recurrent chromosomal deletions have suggested the presence of tumor suppressor genes (TSG) specifically involved in colorectal carcinogenesis. For one of them, two non-overlapping regions have been proposed on the short arm of chromosome 8, encompassing the LPL and NEFL genes. The short arm of chromosome 8 has been extensively studied in colorectal cancer and in other cancer types. Both regions have been reported as candidate loci for a TSG. In order to delineate a reliable region of deletional overlap on chromosome arm 8p in CRC, a series of 365 CRC samples was selected for the absence of microsatellite instability (RER, replication error); tumor and normal matched DNAs were studied for 54 microsatellite polymorphisms distributed on 8p using multiplex-PCR amplification. After purification of tumor nuclei by flow cytometry based on either the abnormal DNA index or the presence of a high expression of cytokeratin, complete allelic losses on 8p were observed in 48% of cases. Measurement of the DNA index showed that 88% of RER tumors were hyperploid. Complete allelic losses of only part of the short arm were observed on 26 occasions. These data allowed us to define a 1 cM interval of common deletion, flanked by the loci D8S1771 and NEFL, where a putative TSG may be localized.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Nucleus / chemistry
  • Chromosome Mapping / methods*
  • Chromosomes, Human, Pair 8 / genetics*
  • Colorectal Neoplasms / genetics*
  • DNA, Neoplasm / analysis
  • Flow Cytometry
  • Genes, Tumor Suppressor / genetics*
  • Genetic Markers / genetics
  • Humans
  • Karyometry
  • Loss of Heterozygosity / genetics*
  • Mice

Substances

  • DNA, Neoplasm
  • Genetic Markers