Multiple regions of allelic loss from chromosome arm 6q in malignant mesothelioma

Daphne W. Bell, Suresh C. Jhanwar, Joseph R. Testa

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Abstract

Our previous cytogenetic studies of malignant mesotheliomas (MMs) revealed losses from 6q15-21 in approximately 40% of cases, suggestive of recurrent loss of function of a putative tumor suppressor gene(s) located in this chromosome region. To more precisely define the critical region of molecular genetic loss within 6q, we have constructed a high-resolution deletion map of this chromosome arm in 46 MMs. We analyzed 32 microsatellite markers to detect loss of heterozygosity in tumor DNAs. Allelic losses from 6q were observed in a high percentage (61%) of cases. Partial deletions of 6q were identified in 11 cases, and these were used to define four nonoverlapping regions of chromosomal loss: a region involving 6q14-21 (~9 cM; 7 of 11 cases with partial deletions), a region within 6q16.3-21 (~8 cM; 9 cases), a region within 6q21-23.2 (~10 cM; 8 cases), and a distal region located at 6q25 (~13 cM; 9 cases). Most cases exhibited losses from more than one of these regions. We conclude from these data that genomic losses involving 6q in MM are more frequent than previously recognized cytogenetically and that the deletions fall into four discrete locations, suggesting the existence of multiple tumor suppressor loci in 6q that may contribute to the pathogenesis of this malignancy.

Original languageEnglish
Pages (from-to)4057-4062
Number of pages6
JournalCancer Research
Volume57
Issue number18
StatePublished - Sep 15 1997

Keywords

  • Alleles
  • Chromosome Deletion
  • Chromosome Mapping
  • Chromosomes, Human, Pair 6
  • Genetic Markers
  • Heterozygote
  • Humans
  • Mesothelioma/genetics
  • Microsatellite Repeats

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