Distinct MDM2 and P14ARF expression and centrosome amplification in well-differentiated liposarcomas
Well‐differentiated liposarcomas (WDLs) are common soft‐tissue tumors in adults. They are characterized by large marker chromosomes and/or ring chromosomes containing 12q‐derived sequences in which MDM2 is consistently amplified. WDLs are subdivided into two subtypes according to their karyotype. Ty...
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Published in: | Genes chromosomes & cancer Vol. 39; no. 2; pp. 99 - 109 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01-02-2004
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Subjects: | |
Online Access: | Get full text |
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Summary: | Well‐differentiated liposarcomas (WDLs) are common soft‐tissue tumors in adults. They are characterized by large marker chromosomes and/or ring chromosomes containing 12q‐derived sequences in which MDM2 is consistently amplified. WDLs are subdivided into two subtypes according to their karyotype. Type D cells exhibit a near‐diploid karyotype, with very few or no chromosome changes. Type H cells exhibit a near‐tetraploid karyotype and many structural changes. Expression of P14ARF, MDM2, and TP53 proteins was assayed in the two WDL subtypes to establish whether distinct expression profiles correlated with cell ploidy. Although a transcriptionally functional TP53 was present in most tumors independent of their karyotype, type H cells were characterized by high levels of P14ARF and MDM2 proteins. Although amplified within similar chromosome markers in type D tumors, MDM2 did not appear to be overexpressed. In addition, it was present as a C‐terminal truncated protein, indicative of alternatively spliced variants of MDM2 mRNA. As the existence of karyotypically distinct tumors could result from alterations of the mitotic machinery, we investigated the centrosome behavior in the two WDL subtypes. Centrosome amplification occurred in WDL tumors types H and D independent of their ploidy status. Moreover, no functional centrosome difference was found between the two tumor subtypes. © 2003 Wiley‐Liss, Inc. |
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Bibliography: | ark:/67375/WNG-0DK18ZLS-Z ArticleID:GCC10303 istex:DA9AA8A26A9E829659EB948CBA0A1848789E7C57 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
ISSN: | 1045-2257 1098-2264 |
DOI: | 10.1002/gcc.10303 |