Publication: Amplification of CDK4, MDM2,
SAS and GLI genes in leiomyosarcoma,
alveolar and embryonal rhabdomyosarcoma
Authors
Ragazzini, P. ; Gamberi, G. ; Pazzaglia, L. ; Serra, M. ; Magagnoli, Giovanna ; Ponticelli, F. ; Ferrari, C. ; Ghinelli, C. ; Alberghini, M. ; Bertoni, F. ; Picci, P. ; Benassi, M.S.
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Publisher
Murcia : F. Hernández
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DOI
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info:eu-repo/semantics/article
Description
Abstract
We evaluated amplification and
overrepresentation of CDK4, MDM2, GLI and SAS
genes of the 12q13-15 region, in a group of soft tissue
sarcomas including leiomyosarcomas (LMS), alveolar
rhabdomyosarcomas (ARMS) and embryonal (anaplastic
and classic variants) rhabdomyosarcomas (ERMS), to
ascertain genomic alterations and possible differences
within histologic subtypes of rhabdomyosarcoma
(RMS).
Quantitative real-time PCR was performed on DNA
samples from 29 LMS, 9 ARMS, 7 anaplastic ERMS
and 6 classic ERMS. Alteration of one or more of the
12q13-15 genes was revealed in 13/29 LMS (45%) and
12/22 RMS (54%) including 5/9 ARMS (56%), 5/7
anaplastic ERMS (71%) and 2/6 classic ERMS (33%).
The potential importance of overproduction of protein
products in neoplastic development, led us also to study
a possible high expression of cdk4, mdm2 and gli
proteins in immunohistochemical staining experiments
on paraffin-embedded tissue samples of the same cases.
Among LMS and RMS most cases with CDK4, MDM2
and GLI gene alterations also showed a simultaneous
high expression of the relative protein.
In summary, these results indicate that amplification
or overerepresentation of genes at 12q13-15 region
involve both LMS and RMS. Moreover these genes
alterations reveal predominantly in the alveolar and in
the anaplastic variant of the embryonal subtype. These
two seem to have a more similar behavior than
anaplastic and classic embryonal that are classified in the
same subtype.
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