Highly frequent allelic loss of chromosome 6q16-23 in osteosarcoma: Involvement of cyclin C in osteosarcoma
The molecular pathogenesis of osteosarcoma is very complicated and associated with chaotic abnormalities on many chromosomal arms. We analyzed 12 cases of osteosarcomas with comparative genomic hybridization (CGH) to identify chromosomal imbalances, and detected highly frequent chromosomal alteratio...
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Published in | International journal of molecular medicine Vol. 18; no. 6; pp. 1153 - 1158 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Greece
D.A. Spandidos
01.12.2006
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Subjects | |
Online Access | Get full text |
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Summary: | The molecular pathogenesis of osteosarcoma is very complicated and associated
with chaotic abnormalities on many chromosomal arms. We analyzed 12 cases of osteosarcomas
with comparative genomic hybridization (CGH) to identify chromosomal imbalances,
and detected highly frequent chromosomal alterations in chromosome 6q, 8p, 10p
and 10q. To define the narrow rearranged region on chromosome 6 with higher resolution,
loss of heterozygosity (LOH) analysis was performed with 21 microsatellite markers.
Out of 31 cases, 23 cases (74%) showed allelic loss at least with one marker on
chromosome 6q. We identified two distinct commonly deleted regions on chromosome
6 using markers D6S1565 located at 6q16 and 6q23MS1 at 6q23. The expression analysis
of genes located at the deleted region was performed, and the decreased mRNA expression
of the CCNC gene, one of the regulators of cell cycle, was detected. Growth of
osteosarcoma cell line was significantly suppressed after the CCNC cDNA transfection.
Fine mapping of the deleted region containing a possible tumor suppressor gene
and the transfection assay suggest that the CCNC is a candidate tumor suppressor
gene. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1107-3756 1791-244X |
DOI: | 10.3892/ijmm.18.6.1153 |