Comparative genomic hybridization as a tool to define two distinct chromosome 12‐derived amplification units in well‐differentiated liposarcomas

Well‐differentiated liposarcomas (WDLPS) are frequently characterized by a near‐diploid karyotype with supernumerary ring and/or giant rod‐shaped marker chromosomes. We have shown, using fluorescence in situ hybridization (FISH) and molecular strategies, that these markers contain chromosome 12‐derived sequences. Here we report the analysis of six WDLPS for the presence of amplified DNA segments by means of the recently developed comparative genomic hybridization (CGH) strategy. Two distinct chromosome 12‐derived amplification units could be identified in all tumors examined, one located in the q 14‐q 15 region as expected, the second unexpectedly mapping to q21.3‐q22. Our results indicate that the concerted amplification of these two distinct regions on the long arm of chromosome 12 may be a consistent characteristic of WDLPS. These amplifications are most likely directly related to the presence of supernumerary ring and/or giant marker chromosomes in this group of soft tissue tumors. Genes Chrom Cancer 9:292‐295 (1994). © 1994 Wiley‐Liss, Inc.

[1]  R. Sinke,et al.  Overrepresentation of chromosome 12p sequences and karyotypic evolution in i(12p)-negative testicular germ-cell tumors revealed by fluorescence in situ hybridization. , 1993, Cancer genetics and cytogenetics.

[2]  P. Cin,et al.  Cytogenetic and fluorescence in situ hybridization investigation of ring chromosomes characterizing a specific pathologic subgroup of adipose tissue tumors. , 1993, Cancer genetics and cytogenetics.

[3]  F. Collin,et al.  Chromosome 12 origin in rings and giant markers in well-differentiated liposarcoma. , 1993, Cancer genetics and cytogenetics.

[4]  P. Meltzer,et al.  Molecular cytogentetic analysis of an amplification unit on chromosome 12q , 1993 .

[5]  F. Mitelman,et al.  Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11) , 1992, Genes, chromosomes & cancer.

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

[7]  L. Looijenga,et al.  Verification of isochromosome 12p and identification of other chromosome 12 aberrations in gonadal and extragonadal human germ cell tumors by bicolor double fluorescence in situ hybridization. , 1992, Cancer genetics and cytogenetics.

[8]  J. Davis,et al.  Analysis of a giant marker chromosome in a well-differentiated liposarcoma using cytogenetics and fluorescence in situ hybridization. , 1992, Cancer genetics and cytogenetics.

[9]  P. Meltzer,et al.  Amplification of a gene encoding a p53-associated protein in human sarcomas , 1992, Nature.

[10]  P. Meltzer,et al.  SAS amplification in soft tissue sarcomas. , 1992, Cancer research.

[11]  S. Leong,et al.  Cytogenetic findings in liposarcoma correlate with histopathologic subtypes , 1992, Cancer.

[12]  P. Meltzer,et al.  Identification and cloning of a novel amplified DNA sequence in human malignant fibrous histiocytoma derived from a region of chromosome 12 frequently rearranged in soft tissue tumors. , 1991, Cell growth & differentiation : the molecular biology journal of the American Association for Cancer Research.

[13]  J. Cassiman,et al.  Demonstration of the genuine iso-12p character of the standard marker chromosome of testicular germ cell tumors and identification of further chromosome 12 aberrations by competitive in situ hybridization. , 1991, American journal of human genetics.

[14]  R. Kucherlapati,et al.  Report of the Third International Workshop on Human Chromosome 12 Mapping 1995. , 1996, Cytogenetics and cell genetics.

[15]  W. V. D. Van de Ven,et al.  Isolation of a somatic cell hybrid retaining the der(16)t(12;16)(q13;p11.2) from a myxoid liposarcoma cell line. , 1993, Cytogenetics and cell genetics.

[16]  J. Rivers Between combine harvester and ribosome , 1975, Nature.