Chromosomal 7q34 duplication and BRAF-KIAA1549 fusion is a characteristic genetic alteration in pilocytic astrocytomas. 7q34 gain appears to be common in diffuse astrocytomas, but its significance is unclear. We assessed BRAF gain and BRAF mutations in 123 low-grade diffuse gliomas, including 55 diffuse astrocytomas, 18 oligoastrocytomas and 50 oligodendrogliomas. Quantitative polymerase chain reaction (PCR) revealed BRAF gain in 17/50 (34%) oligodendrogliomas, a significantly higher frequency than in diffuse astrocytomas (7/55; 13%; P = 0.0112). BRAF gain was common in low-grade diffuse gliomas with 1p/19q loss (39%) and those lacking any of the genetic alterations analyzed (31%), but was rare in those with TP53 mutations (2%). Logistic regression analysis showed a significant positive association between 1p/19q loss and BRAF gain (P = 0.0032) and a significant negative association between TP53 mutations and BRAF gain (P = 0.0042). Fluorescence in situ hybridization (FISH) analysis of 26 low-grade diffuse gliomas with BRAF gain additionally revealed BRAF-KIAA1549 fusion in one oligodendroglioma. Sequencing of cDNA in 17 low-grade diffuse gliomas showed BRAF-KIAA1549 fusion in another oligodendroglioma. A BRAFV600E mutation was also detected in one oligodendroglioma, and a BRAFA598V in one diffuse astrocytoma. These results suggest that low-grade diffuse gliomas with 1p/19q loss have frequent BRAF gains, and a small fraction of oligodendrogliomas may show BRAF-KIAA1549 fusion.

Frequent BRAF Gain in Low-Grade Diffuse Gliomas with 1p/19q Loss / Young Ho, K., Naosuke, N., Werner, P., Benjamin, B., Kathy, K., Ulrich, S., Karsten, W., Luigi, M., Giangaspero, F., Yuko, T., Yoichi, N., Anne, V., Michel, M., Arie, P., Hiroko, O.. - In: BRAIN PATHOLOGY. - ISSN 1015-6305. - ELETTRONICO. - 22:6(2012), pp. 834-840. [10.1111/j.1750-3639.2012.00601.x]

Frequent BRAF Gain in Low-Grade Diffuse Gliomas with 1p/19q Loss

GIANGASPERO, FELICE;
2012

Abstract

Chromosomal 7q34 duplication and BRAF-KIAA1549 fusion is a characteristic genetic alteration in pilocytic astrocytomas. 7q34 gain appears to be common in diffuse astrocytomas, but its significance is unclear. We assessed BRAF gain and BRAF mutations in 123 low-grade diffuse gliomas, including 55 diffuse astrocytomas, 18 oligoastrocytomas and 50 oligodendrogliomas. Quantitative polymerase chain reaction (PCR) revealed BRAF gain in 17/50 (34%) oligodendrogliomas, a significantly higher frequency than in diffuse astrocytomas (7/55; 13%; P = 0.0112). BRAF gain was common in low-grade diffuse gliomas with 1p/19q loss (39%) and those lacking any of the genetic alterations analyzed (31%), but was rare in those with TP53 mutations (2%). Logistic regression analysis showed a significant positive association between 1p/19q loss and BRAF gain (P = 0.0032) and a significant negative association between TP53 mutations and BRAF gain (P = 0.0042). Fluorescence in situ hybridization (FISH) analysis of 26 low-grade diffuse gliomas with BRAF gain additionally revealed BRAF-KIAA1549 fusion in one oligodendroglioma. Sequencing of cDNA in 17 low-grade diffuse gliomas showed BRAF-KIAA1549 fusion in another oligodendroglioma. A BRAFV600E mutation was also detected in one oligodendroglioma, and a BRAFA598V in one diffuse astrocytoma. These results suggest that low-grade diffuse gliomas with 1p/19q loss have frequent BRAF gains, and a small fraction of oligodendrogliomas may show BRAF-KIAA1549 fusion.
2012
diffuse astrocytoma; brafv600e mutation; oligodendroglioma; braf-kiaa1549 fusion gene; braf v600e mutation; braf gain
01 Pubblicazione su rivista::01a Articolo in rivista
Frequent BRAF Gain in Low-Grade Diffuse Gliomas with 1p/19q Loss / Young Ho, K., Naosuke, N., Werner, P., Benjamin, B., Kathy, K., Ulrich, S., Karsten, W., Luigi, M., Giangaspero, F., Yuko, T., Yoichi, N., Anne, V., Michel, M., Arie, P., Hiroko, O.. - In: BRAIN PATHOLOGY. - ISSN 1015-6305. - ELETTRONICO. - 22:6(2012), pp. 834-840. [10.1111/j.1750-3639.2012.00601.x]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/466418
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