Chromosome band 1q21 is recurrently gained in desmoid tumors

DNA sequence copy number changes were studied by comparative genomic hybridization (CGH) in 28 desmoid tumors. Changes were detected in 12 tumors (43%) with a mean of 1.4 changes per sample (range: 1 to 7). Out of 12 tumors associated with pregnancy or Gardner's syndrome, only two displayed changes. The minimal common regions of the most frequent gains were 1q21 (39%), chromosome 20 (32%), and 9p12 (21%). No high‐level amplifications were detected. Losses of DNA sequences were two times less frequent than gains and the minimal common regions of the most frequent losses were 6q16–q21 (14%), 5q14 (11%), and 13q21–q31 (11%). Genes Chromosomes Cancer 23:183–186, 1998. © 1998 Wiley‐Liss, Inc.

[1]  S. Knuutila,et al.  DNA copy number amplifications in human neoplasms: review of comparative genomic hybridization studies. , 1998, The American journal of pathology.

[2]  S. Knuutila,et al.  Optimization of comparative genomic hybridization using fluorochrome conjugated to dCTP and dUTP nucleotides. , 1997, Laboratory investigation; a journal of technical methods and pathology.

[3]  S. Knuutila,et al.  Comparative genomic hybridization of malignant fibrous histiocytoma reveals a novel prognostic marker. , 1997, The American journal of pathology.

[4]  S. Knuutila,et al.  Gains, losses, and amplifications of DNA sequences evaluated by comparative genomic hybridization in chondrosarcomas. , 1997, The American journal of pathology.

[5]  P. van Eyken,et al.  Trisomies 8 and 20 in desmoid tumors. , 1996, Cancer genetics and cytogenetics.

[6]  A. Sandberg,et al.  Deletion 5q in desmoid tumor and fluorescence in situ hybridization for chromosome 8 and/or 20 copy number. , 1996, Cancer genetics and cytogenetics.

[7]  J. Barber,et al.  Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene. , 1996, American journal of human genetics.

[8]  R. Phillips,et al.  Desmoids in familial adenomatous polyposis , 1996, The British journal of surgery.

[9]  O. Myklebost,et al.  Characterisation of a novel amplicon at 1q21-q22 in human sarcomas by CGH and molecular analysis , 1996 .

[10]  F. Mitelman,et al.  Catalog of Chromosome Aberrations in Cancer , 1996, British Journal of Cancer.

[11]  S. Knuutila,et al.  Gains and losses of DNA sequences in liposarcomas evaluated by comparative genomic hybridization , 1996, Genes, chromosomes & cancer.

[12]  F. Mitelman,et al.  Trisomy 20 is a primary chromosome aberration in desmoid tumors , 1995, International journal of cancer.

[13]  T. Akiyama,et al.  The tumour suppressor gene product APC blocks cell cycle progression from G0/G1 to S phase. , 1995, The EMBO journal.

[14]  S. Knuutila,et al.  Gains and losses of DNA sequences in osteosarcomas by comparative genomic hybridization. , 1995, Cancer research.

[15]  J. Fletcher,et al.  Chromosome aberrations in desmoid tumors. Trisomy 8 may be a predictor of recurrence. , 1995, Cancer genetics and cytogenetics.

[16]  R. Sciot,et al.  Trisomy 20 characterizes a second group of desmoid tumors. , 1995, Cancer genetics and cytogenetics.

[17]  P. Polakis Mutations in the APC gene and their implications for protein structure and function. , 1995, Current opinion in genetics & development.

[18]  H. Lynch,et al.  Deletion (5q) in a desmoid tumor of a patient with Gardner's syndrome. , 1994, Cancer genetics and cytogenetics.

[19]  J. Delabie,et al.  Some desmoid tumors are characterized by trisomy 8 , 1994, Genes, chromosomes & cancer.

[20]  D. Pinkel,et al.  Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid Tumors , 1992 .

[21]  A. Sandberg,et al.  Clonal chromosomal abnormalities in desmoid tumors. Implications for histopathogenesis , 1992, Cancer.

[22]  S. Altschul,et al.  Identification of FAP locus genes from chromosome 5q21. , 1991, Science.

[23]  F. Mitelman,et al.  Complex chromosome rearrangements in an extraabdominal desmoid tumor. , 1988, Cancer genetics and cytogenetics.

[24]  Shirley A. Miller,et al.  A simple salting out procedure for extracting DNA from human nucleated cells. , 1988, Nucleic acids research.

[25]  F. C. Lucibello,et al.  Localization of the gene for familial adenomatous polyposis on chromosome 5 , 1987, Nature.

[26]  O. Myklebost,et al.  Recurrent gains of 1q, 8 and 12 in the Ewing family of tumours by comparative genomic hybridization. , 1997, British Journal of Cancer.

[27]  H. Järvinen,et al.  Occurrence of desmoid tumours in familial adenomatous polyposis and results of treatment , 1996, International Journal of Colorectal Disease.