TY - JOUR
T1 - Molecular heterogeneity in glioblastoma
T2 - Therapeutic opportunities and challenges
AU - Nicholas, M. Kelly
AU - Lukas, Rimas V.
AU - Chmura, Steven
AU - Yamini, Bakhtihar
AU - Lesniak, MacIej
AU - Pytel, Peter
PY - 2011/4
Y1 - 2011/4
N2 - Glioblastoma (GBM) has been recognized as a clinical and pathologic entity for more than a century. Throughout its history, its cells of origin have been in question. Its behavior is aggressive and despite decades of effort, median survival is just beginning to improve. Surgical techniques and radiotherapy schemas continue to be refined, but the most recent progress has been achieved through improved medical therapies. These are the result of both pharmacological advances and a deeper understanding of the biological characteristics of GBM. Due to a combination of its complex phenotype and organ-specific clinical manifestations, efforts to refine GBM treatment with targeted therapies largely have been frustrated. In this review, we discuss recent attempts to exploit new molecular insights, consider the reasons for slow progress in developing better treatments, and examine future therapeutic options.
AB - Glioblastoma (GBM) has been recognized as a clinical and pathologic entity for more than a century. Throughout its history, its cells of origin have been in question. Its behavior is aggressive and despite decades of effort, median survival is just beginning to improve. Surgical techniques and radiotherapy schemas continue to be refined, but the most recent progress has been achieved through improved medical therapies. These are the result of both pharmacological advances and a deeper understanding of the biological characteristics of GBM. Due to a combination of its complex phenotype and organ-specific clinical manifestations, efforts to refine GBM treatment with targeted therapies largely have been frustrated. In this review, we discuss recent attempts to exploit new molecular insights, consider the reasons for slow progress in developing better treatments, and examine future therapeutic options.
UR - http://www.scopus.com/inward/record.url?scp=79952947661&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79952947661&partnerID=8YFLogxK
U2 - 10.1053/j.seminoncol.2011.01.009
DO - 10.1053/j.seminoncol.2011.01.009
M3 - Article
C2 - 21421114
AN - SCOPUS:79952947661
SN - 0093-7754
VL - 38
SP - 243
EP - 253
JO - Seminars in Oncology
JF - Seminars in Oncology
IS - 2
ER -