Kurani Hetakshi, Gurav Mamta, Shetty Omshree, Chinnaswamy Girish, Moiyadi Aliasagar, Gupta Tejpal, Jalali Rakesh, Epari Sridhar
Division of Molecular Pathology, Department of Pathology, Tata Memorial Centre, Homi Baba National Institute, Mumbai, 400012, India.
Department of Pediatric Oncology, Tata Memorial Centre, Homi Baba National Institute, Mumbai, 400012, India.
Childs Nerv Syst. 2019 Sep;35(9):1525-1536. doi: 10.1007/s00381-019-04282-1. Epub 2019 Jul 18.
Pilocytic astrocytomas (PCAs) are characterized by two dominant molecular alterations of the BRAF gene, i.e., BRAFV600E mutation and KIAA1549-BRAF fusions which show a differential pattern of frequency across different age-groups.
Formalin-fixed paraffin-embedded tissues of 358 (pediatric 276 and adult 82) consecutive PCAs were evaluated for BRAFV600E mutation by Sanger sequencing and KIAA1549:BRAF fusion transcripts (KIAA1549:BRAF 16-9, KIAA1549:BRAF 15-9, and KIAA1549:BRAF 16-11) by reverse transcriptase polymerase chain reaction, which were correlated with different clinicopathological features.
BRAFV600E mutation was detected in 8.9% pediatric and 9.75% adult PCAs, whereas 41.1% and 25.7% of pediatric and adult cases showed KIAA1549-BRAF fusions respectively. BRAFV600E did not show any statistically significant correlation with any of the clinical parameters (age, location, and gender). KIAA1549:BRAF fusions showed a significant statistical association with the pediatric age group and cerebellar location. KIAA1549-BRAF 16-9 was the commonest variant and was predominantly associated with cerebellar location than non-cerebellar whereas fusion variant 15-9 negatively correlated with cerebellar locations.
The present study showed overall frequency of 53.5% and 37.3% BRAF alterations in pediatric and adult PCA cases respectively. BRAF fusion in PCA cases showed a different distribution pattern across age groups and locations; while no such differential pattern was observed for BRAFV600E.
毛细胞型星形细胞瘤(PCA)的特征是BRAF基因有两种主要的分子改变,即BRAFV600E突变和KIAA1549 - BRAF融合,这两种改变在不同年龄组中的频率模式有所不同。
对358例连续的PCA(儿童276例,成人82例)的福尔马林固定石蜡包埋组织进行评估,通过桑格测序检测BRAFV600E突变,通过逆转录聚合酶链反应检测KIAA1549:BRAF融合转录本(KIAA1549:BRAF 16 - 9、KIAA1549:BRAF 15 - 9和KIAA1549:BRAF 16 - 11),并将其与不同的临床病理特征相关联。
在儿童PCA中检测到BRAFV600E突变的比例为8.9%,成人PCA中为9.75%,而儿童和成人病例中分别有41.1%和25.7%显示KIAA1549 - BRAF融合。BRAFV600E与任何临床参数(年龄、位置和性别)均无统计学显著相关性。KIAA1549:BRAF融合与儿童年龄组和小脑位置有显著统计学关联。KIAA1549 - BRAF 16 - 9是最常见的变异体,主要与小脑位置相关,而非小脑位置较少见,而融合变异体15 - 9与小脑位置呈负相关。
本研究显示儿童和成人PCA病例中BRAF改变的总体频率分别为53.5%和37.3%。PCA病例中的BRAF融合在不同年龄组和位置显示出不同的分布模式;而BRAFV600E未观察到这种差异模式。