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Genetic and expression profiles of cerebellar liponeurocytomas

Genetic and expression profiles of cerebellar liponeurocytomas
Genetic and expression profiles of cerebellar liponeurocytomas
Cerebellar liponeurocytoma, a rare, newly identified CNS neoplasm of adults, is characterized by advanced neuronal/neurocytic and focal lipomatous differentiation, low proliferative potential and a favorable clinical prognosis. Despite the different age distribution and benign biological behavior, the cerebellar liponeurocytoma shares several features with the cerebellar medulloblastoma, which may include an origin from the periventricular matrix of the fourth ventricle or the external granular layer of the cerebellum. To establish the genetic profile of cerebellar liponeurocytomas, we have formed an international consortium and collected tumor samples from 20 patients. DNA sequencing revealed TP53 missense mutations in 4 (20%) of 20 cerebellar liponeurocytomas, a frequency higher than in medulloblastomas. There was no case with PTCH, APC, or -catenin mutations, each of which may be present in subsets of medulloblastomas. Isochromosome 17q, a genetic hallmark of classic medulloblastomas, was not observed in any of the cases investigated by FISH analysis. cDNA array analyses were carried out on 4 cerebellar liponeurocytomas, 4 central neurocytomas, and 4 classic medulloblastomas. Cluster analysis of the cDNA expression data of 1176 genes grouped cerebellar liponeurocytomas close to central neurocytomas, but distinct from medulloblastomas. These results suggest cerebellar liponeurocytoma as a distinct tumor entity that is genetically different from medulloblastoma. Furthermore, the cDNA expression array data suggest a relationship to central neurocytomas, but the presence of TP53 mutations, which are absent in central neurocytomas, suggests that their genetic pathways are different.
281-289
Horstmann, Sonia
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Perry, Arie
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Reifenberger, Guido
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Giangaspero, Felice
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Huang, Herve
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Hara, Akira
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Masuoka, Jun
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Rainov, Nikolai G.
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Bergmann, Markus
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Heppner, Frank L.
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Brandner, Sebastian
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Chimelli, Leila
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Montagna, Nadia
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Jackson, Thad
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Davis, Daron G.
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Markesbery, William R.
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Ellison, David W.
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Weller, Roy O.
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Taddei, Gian L.
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Conti, Renato
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Del Bigio, Marc R.
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Gonzalez-Campora, Ricardo
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Radhakrishnan, V.V.
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Soylemzoglu, Figen
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Uro-Coste, Emmanuelle
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Qian, Jiang
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Kleihues, Paul
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Ohgaki, Hiroko
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Horstmann, Sonia
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Perry, Arie
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Reifenberger, Guido
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Giangaspero, Felice
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Huang, Herve
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Hara, Akira
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Masuoka, Jun
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Rainov, Nikolai G.
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Bergmann, Markus
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Heppner, Frank L.
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Brandner, Sebastian
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Chimelli, Leila
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Montagna, Nadia
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Jackson, Thad
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Davis, Daron G.
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Markesbery, William R.
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Ellison, David W.
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Weller, Roy O.
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Taddei, Gian L.
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Conti, Renato
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Del Bigio, Marc R.
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Gonzalez-Campora, Ricardo
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Radhakrishnan, V.V.
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Soylemzoglu, Figen
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Uro-Coste, Emmanuelle
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Qian, Jiang
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Kleihues, Paul
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Ohgaki, Hiroko
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Horstmann, Sonia, Perry, Arie, Reifenberger, Guido, Giangaspero, Felice, Huang, Herve, Hara, Akira, Masuoka, Jun, Rainov, Nikolai G., Bergmann, Markus, Heppner, Frank L., Brandner, Sebastian, Chimelli, Leila, Montagna, Nadia, Jackson, Thad, Davis, Daron G., Markesbery, William R., Ellison, David W., Weller, Roy O., Taddei, Gian L., Conti, Renato, Del Bigio, Marc R., Gonzalez-Campora, Ricardo, Radhakrishnan, V.V., Soylemzoglu, Figen, Uro-Coste, Emmanuelle, Qian, Jiang, Kleihues, Paul and Ohgaki, Hiroko (2004) Genetic and expression profiles of cerebellar liponeurocytomas. Brain Pathology, 14 (3), 281-289.

Record type: Article

Abstract

Cerebellar liponeurocytoma, a rare, newly identified CNS neoplasm of adults, is characterized by advanced neuronal/neurocytic and focal lipomatous differentiation, low proliferative potential and a favorable clinical prognosis. Despite the different age distribution and benign biological behavior, the cerebellar liponeurocytoma shares several features with the cerebellar medulloblastoma, which may include an origin from the periventricular matrix of the fourth ventricle or the external granular layer of the cerebellum. To establish the genetic profile of cerebellar liponeurocytomas, we have formed an international consortium and collected tumor samples from 20 patients. DNA sequencing revealed TP53 missense mutations in 4 (20%) of 20 cerebellar liponeurocytomas, a frequency higher than in medulloblastomas. There was no case with PTCH, APC, or -catenin mutations, each of which may be present in subsets of medulloblastomas. Isochromosome 17q, a genetic hallmark of classic medulloblastomas, was not observed in any of the cases investigated by FISH analysis. cDNA array analyses were carried out on 4 cerebellar liponeurocytomas, 4 central neurocytomas, and 4 classic medulloblastomas. Cluster analysis of the cDNA expression data of 1176 genes grouped cerebellar liponeurocytomas close to central neurocytomas, but distinct from medulloblastomas. These results suggest cerebellar liponeurocytoma as a distinct tumor entity that is genetically different from medulloblastoma. Furthermore, the cDNA expression array data suggest a relationship to central neurocytomas, but the presence of TP53 mutations, which are absent in central neurocytomas, suggests that their genetic pathways are different.

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Published date: July 2004

Identifiers

Local EPrints ID: 27603
URI: http://eprints.soton.ac.uk/id/eprint/27603
PURE UUID: 744c0af6-089f-47e2-a6e7-6cd1d3f4faa4

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Date deposited: 27 Apr 2006
Last modified: 09 Jan 2022 01:22

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Contributors

Author: Sonia Horstmann
Author: Arie Perry
Author: Guido Reifenberger
Author: Felice Giangaspero
Author: Herve Huang
Author: Akira Hara
Author: Jun Masuoka
Author: Nikolai G. Rainov
Author: Markus Bergmann
Author: Frank L. Heppner
Author: Sebastian Brandner
Author: Leila Chimelli
Author: Nadia Montagna
Author: Thad Jackson
Author: Daron G. Davis
Author: William R. Markesbery
Author: David W. Ellison
Author: Roy O. Weller
Author: Gian L. Taddei
Author: Renato Conti
Author: Marc R. Del Bigio
Author: Ricardo Gonzalez-Campora
Author: V.V. Radhakrishnan
Author: Figen Soylemzoglu
Author: Emmanuelle Uro-Coste
Author: Jiang Qian
Author: Paul Kleihues
Author: Hiroko Ohgaki

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