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Erschienen in: Cellular Oncology 4/2011

01.08.2011 | Original Paper

Genetic profile of adenoid cystic carcinomas (ACC) with high-grade transformation versus solid type

verfasst von: Ana Flávia Costa, Albina Altemani, Hedy Vékony, Elisabeth Bloemena, Florentino Fresno, Carlos Suárez, José Luis Llorente, Mario Hermsen

Erschienen in: Cellular Oncology | Ausgabe 4/2011

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Abstract

Background

ACC can occasionally undergo dedifferentiation also referred to as high-grade transformation (ACC-HGT). However, ACC-HGT can also undergo transformation to adenocarcinomas which are not poorly differentiated. ACC-HGT is generally considered to be an aggressive variant of ACC, even more than solid ACC. This study was aimed to describe the genetic changes of ACC-HGT in relation to clinico-pathological features, and to compare results to solid ACC.

Methods

Genome wide DNA copy number changes were analyzed by microarray CGH in ACC-HGT, four with transformation into moderately differentiated adenocarcinoma (MDA) and two into poorly differentiated carcinoma (PDC), and five solid ACC. In addition, Ki67 index and p53 immunopositivity was assessed.

Results

ACC-HGT carried fewer copy number changes compared to solid ACC. Two ACC-HGT cases harboured a breakpoint at 6q23, near the cMYB oncogene. The complexity of the genomic profile concurred with the clinical course of the patient. Among the ACC-HGT, p53 positivity significantly increased from the conventional to the transformed (both MDA and PDC) component.

Conclusion

ACC-HGT may not necessarily reflect a more advanced stage of tumor progression, but rather a transformation to another histological form in which the poorly differentiated forms (PDC) presents a genetic complexity similar to the solid ACC.
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Metadaten
Titel
Genetic profile of adenoid cystic carcinomas (ACC) with high-grade transformation versus solid type
verfasst von
Ana Flávia Costa
Albina Altemani
Hedy Vékony
Elisabeth Bloemena
Florentino Fresno
Carlos Suárez
José Luis Llorente
Mario Hermsen
Publikationsdatum
01.08.2011
Verlag
Springer Netherlands
Erschienen in
Cellular Oncology / Ausgabe 4/2011
Print ISSN: 2211-3428
Elektronische ISSN: 2211-3436
DOI
https://doi.org/10.1007/s13402-011-0037-5

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