{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,30]],"date-time":"2026-05-30T09:03:01Z","timestamp":1780131781843,"version":"3.54.0"},"reference-count":60,"publisher":"Journal of Neurosurgery Publishing Group (JNSPG)","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2018,6]]},"abstract":"<jats:p>\n                    Meningiomas are among the most common intracranial pathological conditions, accounting for 36% of intracranial lesions treated by neurosurgeons. Although the majority of these lesions are benign, the classical categorization of tumors by histological type or World Health Organization (WHO) grade has not fully captured the potential for meningioma progression and recurrence. Many targeted treatments have failed to generate a long-lasting effect on these tumors. Recently, several seminal studies evaluating the genomics of intracranial meningiomas have rapidly changed the understanding of the disease. The importance of\n                    <jats:italic>NF2<\/jats:italic>\n                    (neurofibromin 2),\n                    <jats:italic>TRAF7<\/jats:italic>\n                    (tumor necrosis factor [TNF] receptor\u2013associated factor 7),\n                    <jats:italic>KLF4<\/jats:italic>\n                    (Kruppel-like factor 4),\n                    <jats:italic>AKT1<\/jats:italic>\n                    ,\n                    <jats:italic>SMO<\/jats:italic>\n                    (smoothened),\n                    <jats:italic>PIK3CA<\/jats:italic>\n                    (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha), and\n                    <jats:italic>POLR2<\/jats:italic>\n                    (RNA polymerase II subunit A) demonstrates that there are at least 6 distinct mutational classes of meningiomas. In addition, 6 methylation classes of meningioma have been appreciated, enabling improved prediction of prognosis compared with traditional WHO grades. Genomic studies have shed light on the nature of recurrent meningioma, distinct intracranial locations and mutational patterns, and a potential embryonic cancer stem cell\u2013like origin. However, despite these exciting findings, the clinical relevance of these findings remains elusive. The authors review the key findings from recent genomic studies in meningiomas, specifically focusing on how these findings relate to clinical insights for the practicing neurosurgeon.\n                  <\/jats:p>","DOI":"10.3171\/2018.2.focus1849","type":"journal-article","created":{"date-parts":[[2018,6,1]],"date-time":"2018-06-01T03:36:59Z","timestamp":1527824219000},"page":"E10","source":"Crossref","is-referenced-by-count":40,"title":["Clinical potential of meningioma genomic insights: a practical review for neurosurgeons"],"prefix":"10.3171","volume":"44","author":[{"given":"Michael","family":"Karsy","sequence":"first","affiliation":[{"name":"Department of Neurosurgery, Clinical Neurosciences Center, and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mohammed A.","family":"Azab","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Clinical Neurosciences Center, and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Hussam","family":"Abou-Al-Shaar","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Clinical Neurosciences Center, and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jian","family":"Guan","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Clinical Neurosciences Center, and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ilyas","family":"Eli","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Clinical Neurosciences Center, and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Randy L.","family":"Jensen","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, Clinical Neurosciences Center, and"},{"name":"Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah; and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"D. Ryan","family":"Ormond","sequence":"additional","affiliation":[{"name":"Department of Neurosurgery, University of Colorado School of Medicine, Aurora, Colorado"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1754","reference":[{"key":"b1","series-title":"Acta Neurochir (Wien)","first-page":"447","article-title":"Gene expression profiling of meningiomas: current status after a decade of microarray-based transcriptomic studies","volume":"153","author":"Aarhus M","year":"2011","unstructured":"Aarhus M, Lund-Johansen M, Knappskog PM: Gene expression profiling of meningiomas: current status after a decade of microarray-based transcriptomic studies. 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