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- W29398439 endingPage "30" @default.
- W29398439 startingPage "15" @default.
- W29398439 abstract "The tumors classified as gliomas include a wide variety of histologies including the more common (astrocytoma, glioblastoma), as well as the less common histologies (oligodendroglioma, mixed oligoastrocytoma, pilocytic astrocytoma). Recent efforts at comprehensive genetic characterization of various primary brain tumor types have identified a number of common alterations and pathways common to multiple tumor types. Common pathways in glioma biology include growth factor receptor tyrosine kinases and their downstream signaling via the MAP kinase cascade or PI3K signaling, loss of apoptosis through p53, cell cycle regulation, angiogenesis via VEGF signaling, and invasion. However, in addition to these common general pathway alterations, a number of specific alterations have been identified in particular tumor types, and a number of these have direct therapeutic implications. These include mutations or fusions in the BRAF gene seen in pilocytic astrocytomas (and gangliogliomas). In oligodendrogliomas, mutations in IDH1 and codeletion of chromosomes 1p and 19q are associated with improved survival with upfront use of combined chemotherapy and radiation, and these tumors also have unique mutations of CIC and FUBP1 genes. Low grade gliomas are increasingly seen to be divided into two groups based on IDH mutation status, with astrocytomas developing through IDH mutation followed by p53 mutation, while poor prognosis low grade gliomas and primary glioblastomas (GBMs) are characterized by EGFR amplification, loss of PTEN, and loss of cyclin-dependent kinase inhibitors. GBMs can be further characterized based on gene expression and gene methylation patterns into three or four distinct subgroups. Prognostic markers in diffuse gliomas include IDH mutation, 1p/19q codeletion, and MGMT methylation, and MGMT is also a predictive marker in elderly patients with glioblastoma treated with temozolomide monotherapy." @default.
- W29398439 created "2016-06-24" @default.
- W29398439 creator A5029624096 @default.
- W29398439 creator A5047608444 @default.
- W29398439 date "2014-12-03" @default.
- W29398439 modified "2023-10-14" @default.
- W29398439 title "Glioma Biology and Molecular Markers" @default.
- W29398439 cites W1485875137 @default.
- W29398439 cites W1921809757 @default.
- W29398439 cites W1964150693 @default.
- W29398439 cites W1969013165 @default.
- W29398439 cites W1976934522 @default.
- W29398439 cites W1976979641 @default.
- W29398439 cites W1978775082 @default.
- W29398439 cites W1982088425 @default.
- W29398439 cites W1996908572 @default.
- W29398439 cites W1999831372 @default.
- W29398439 cites W2005036868 @default.
- W29398439 cites W2012768021 @default.
- W29398439 cites W2014006702 @default.
- W29398439 cites W2015469768 @default.
- W29398439 cites W2018093166 @default.
- W29398439 cites W2019879146 @default.
- W29398439 cites W2020277292 @default.
- W29398439 cites W2022064821 @default.
- W29398439 cites W2023393975 @default.
- W29398439 cites W2024672608 @default.
- W29398439 cites W2025183726 @default.
- W29398439 cites W2028516762 @default.
- W29398439 cites W2035409103 @default.
- W29398439 cites W2039075677 @default.
- W29398439 cites W2039945243 @default.
- W29398439 cites W2040827479 @default.
- W29398439 cites W2040992341 @default.
- W29398439 cites W2041480426 @default.
- W29398439 cites W2043129534 @default.
- W29398439 cites W2043732412 @default.
- W29398439 cites W2049281642 @default.
- W29398439 cites W2053300826 @default.
- W29398439 cites W2053535808 @default.
- W29398439 cites W2055560959 @default.
- W29398439 cites W2058355285 @default.
- W29398439 cites W2074591493 @default.
- W29398439 cites W2078972833 @default.
- W29398439 cites W2080452140 @default.
- W29398439 cites W2083599957 @default.
- W29398439 cites W2086216067 @default.
- W29398439 cites W2088813072 @default.
- W29398439 cites W2099603826 @default.
- W29398439 cites W2100795816 @default.
- W29398439 cites W2101332957 @default.
- W29398439 cites W2104669585 @default.
- W29398439 cites W2105100844 @default.
- W29398439 cites W2105528101 @default.
- W29398439 cites W2106234246 @default.
- W29398439 cites W2107731988 @default.
- W29398439 cites W2109816625 @default.
- W29398439 cites W2112495947 @default.
- W29398439 cites W2113942802 @default.
- W29398439 cites W2114098415 @default.
- W29398439 cites W2117577687 @default.
- W29398439 cites W2119836524 @default.
- W29398439 cites W2120963683 @default.
- W29398439 cites W2123764128 @default.
- W29398439 cites W2124620305 @default.
- W29398439 cites W2126744367 @default.
- W29398439 cites W2126817554 @default.
- W29398439 cites W2131177535 @default.
- W29398439 cites W2131724940 @default.
- W29398439 cites W2131860315 @default.
- W29398439 cites W2133865472 @default.
- W29398439 cites W2135947790 @default.
- W29398439 cites W2140048538 @default.
- W29398439 cites W2140892567 @default.
- W29398439 cites W2141113918 @default.
- W29398439 cites W2141410747 @default.
- W29398439 cites W2143078369 @default.
- W29398439 cites W2143619463 @default.
- W29398439 cites W2144003562 @default.
- W29398439 cites W2145489645 @default.
- W29398439 cites W2147013683 @default.
- W29398439 cites W2149814701 @default.
- W29398439 cites W2150200928 @default.
- W29398439 cites W2150638747 @default.
- W29398439 cites W2150929170 @default.
- W29398439 cites W2154526619 @default.
- W29398439 cites W2158681922 @default.
- W29398439 cites W2159753905 @default.
- W29398439 cites W2159842626 @default.
- W29398439 cites W2160300695 @default.
- W29398439 cites W2160382843 @default.
- W29398439 cites W2161289668 @default.
- W29398439 cites W2165438710 @default.
- W29398439 cites W2165648250 @default.
- W29398439 cites W2168784615 @default.
- W29398439 cites W2169438753 @default.
- W29398439 cites W4242403727 @default.
- W29398439 doi "https://doi.org/10.1007/978-3-319-12048-5_2" @default.