%0 Journal Article %1 Park:2017:J-Pathol-Transl-Med:28535583 %A Park, S H %A Won, J %A Kim, S I %A Lee, Y %A Park, C K %A Kim, S K %A Choi, S H %D 2017 %J J Pathol Transl Med %K SHOULDREAD astrocytoma fulltext glioblastoma glioma molecular-testing who %N 3 %P 205-223 %R 10.4132/jptm.2017.03.08 %T Molecular Testing of Brain Tumor %U https://www.ncbi.nlm.nih.gov/pubmed/28535583 %V 51 %X The World Health Organization (WHO) classification of central nervous system (CNS) tumors was revised in 2016 with a basis on the integrated diagnosis of molecular genetics. We herein provide the guidelines for using molecular genetic tests in routine pathological practice for an accurate diagnosis and appropriate management. While astrocytomas and IDH-mutant (secondary) glioblastomas are characterized by the mutational status of IDH, TP53 , and ATRX , oligodendrogliomas have a 1p/19q codeletion and mutations in IDH, CIC , FUBP1 , and the promoter region of telomerase reverse transcriptase ( TERTp ). IDH-wildtype (primary) glioblastomas typically lack mutations in IDH, but are characterized by copy number variations of EGFR, PTEN, CDKN2A/B, PDGFRA , and NF1 as well as mutations of TERTp . High-grade pediatric gliomas differ from those of adult gliomas, consisting of mutations in H3F3A, ATRX , and DAXX , but not in IDH genes. In contrast, well-circumscribed low-grade neuroepithelial tumors in children, such as pilocytic astrocytoma, pleomorphic xanthoastrocytoma, and ganglioglioma, often have mutations or activating rearrangements in the BRAF, FGFR1, and MYB genes. Other CNS tumors, such as ependymomas, neuronal and glioneuronal tumors, embryonal tumors, meningothelial, and other mesenchymal tumors have important genetic alterations, many of which are diagnostic, prognostic, and predictive markers and therapeutic targets. Therefore, the neuropathological evaluation of brain tumors is increasingly dependent on molecular genetic tests for proper classification, prediction of biological behavior and patient management. Identifying these gene abnormalities requires cost-effective and high-throughput testing, such as next-generation sequencing. Overall, this paper reviews the global guidelines and diagnostic algorithms for molecular genetic testing of brain tumors.

@article{Park:2017:J-Pathol-Transl-Med:28535583, abstract = {The World Health Organization (WHO) classification of central nervous system (CNS) tumors was revised in 2016 with a basis on the integrated diagnosis of molecular genetics. We herein provide the guidelines for using molecular genetic tests in routine pathological practice for an accurate diagnosis and appropriate management. While astrocytomas and IDH-mutant (secondary) glioblastomas are characterized by the mutational status of IDH, TP53 , and ATRX , oligodendrogliomas have a 1p/19q codeletion and mutations in IDH, CIC , FUBP1 , and the promoter region of telomerase reverse transcriptase ( TERTp ). IDH-wildtype (primary) glioblastomas typically lack mutations in IDH, but are characterized by copy number variations of EGFR, PTEN, CDKN2A/B, PDGFRA , and NF1 as well as mutations of TERTp . High-grade pediatric gliomas differ from those of adult gliomas, consisting of mutations in H3F3A, ATRX , and DAXX , but not in IDH genes. In contrast, well-circumscribed low-grade neuroepithelial tumors in children, such as pilocytic astrocytoma, pleomorphic xanthoastrocytoma, and ganglioglioma, often have mutations or activating rearrangements in the BRAF, FGFR1, and MYB genes. Other CNS tumors, such as ependymomas, neuronal and glioneuronal tumors, embryonal tumors, meningothelial, and other mesenchymal tumors have important genetic alterations, many of which are diagnostic, prognostic, and predictive markers and therapeutic targets. Therefore, the neuropathological evaluation of brain tumors is increasingly dependent on molecular genetic tests for proper classification, prediction of biological behavior and patient management. Identifying these gene abnormalities requires cost-effective and high-throughput testing, such as next-generation sequencing. Overall, this paper reviews the global guidelines and diagnostic algorithms for molecular genetic testing of brain tumors.}, added-at = {2017-09-10T23:10:51.000+0200}, author = {Park, S H and Won, J and Kim, S I and Lee, Y and Park, C K and Kim, S K and Choi, S H}, biburl = {https://www.bibsonomy.org/bibtex/28495dd2ed300014ae10a0ddf19ec65aa/marcsaric}, description = {Molecular Testing of Brain Tumor. - PubMed - NCBI}, doi = {10.4132/jptm.2017.03.08}, interhash = {7f44a3919bed663275f8783c9d1b8a15}, intrahash = {8495dd2ed300014ae10a0ddf19ec65aa}, journal = {J Pathol Transl Med}, keywords = {SHOULDREAD astrocytoma fulltext glioblastoma glioma molecular-testing who}, month = may, number = 3, pages = {205-223}, pmid = {28535583}, timestamp = {2017-09-10T23:10:51.000+0200}, title = {Molecular Testing of Brain Tumor}, url = {https://www.ncbi.nlm.nih.gov/pubmed/28535583}, volume = 51, year = 2017 }