TY - JOUR
T1 - Targeting Glioblastoma
T2 - Advances in Drug Delivery and Novel Therapeutic Approaches
AU - Yeini, Eilam
AU - Ofek, Paula
AU - Albeck, Nitzan
AU - Rodriguez Ajamil, Daniel
AU - Neufeld, Lena
AU - Eldar-Boock, Anat
AU - Kleiner, Ron
AU - Vaskovich, Daniella
AU - Koshrovski-Michael, Shani
AU - Israeli Dangoor, Sahar
AU - Krivitsky, Adva
AU - Burgos Luna, Christian
AU - Shenbach-Koltin, Gal
AU - Goldenfeld, Miki
AU - Hadad, Ori
AU - Tiram, Galia
AU - Satchi-Fainaro, Ronit
N1 - Publisher Copyright:
© 2020 The Authors. Published by Wiley-VCH GmbH
PY - 2021/1
Y1 - 2021/1
N2 - Glioblastoma (GB) is the most lethal type of primary tumor in the central nervous system. Current treatments include surgical resection followed by chemotherapy and radiotherapy. With this therapeutic regimen, the median survival is less than two years. However, these treatments do not much improve the overall survival of GB patients. GBs are highly angiogenic and invasive tumors and often acquire resistance to therapy. The invasive nature of the disease limits the ability to achieve complete resection of the tumor and the majority of GB patients will experience disease relapse. Moreover, GB is highly heterogeneous, harboring different mutations and presenting different phenotypes. As the brain is considered to be an immune-privileged tissue, GB is defined as a cold tumor for which current immunotherapies have not yet been demonstrated to improve survival. On top of these challenges, the blood brain barrier (BBB) restricts the uptake of drugs by the brain, thus limiting the therapeutic options. Therefore, enormous efforts are being dedicated to the development of novel nanomedicines, which will be able to cross the BBB and specifically target the cancer cells. Here, the current achievements in drug delivery and novel therapeutic approaches for GB therapy are discussed.
AB - Glioblastoma (GB) is the most lethal type of primary tumor in the central nervous system. Current treatments include surgical resection followed by chemotherapy and radiotherapy. With this therapeutic regimen, the median survival is less than two years. However, these treatments do not much improve the overall survival of GB patients. GBs are highly angiogenic and invasive tumors and often acquire resistance to therapy. The invasive nature of the disease limits the ability to achieve complete resection of the tumor and the majority of GB patients will experience disease relapse. Moreover, GB is highly heterogeneous, harboring different mutations and presenting different phenotypes. As the brain is considered to be an immune-privileged tissue, GB is defined as a cold tumor for which current immunotherapies have not yet been demonstrated to improve survival. On top of these challenges, the blood brain barrier (BBB) restricts the uptake of drugs by the brain, thus limiting the therapeutic options. Therefore, enormous efforts are being dedicated to the development of novel nanomedicines, which will be able to cross the BBB and specifically target the cancer cells. Here, the current achievements in drug delivery and novel therapeutic approaches for GB therapy are discussed.
KW - blood brain barrier
KW - drug delivery
KW - glioblastoma
KW - nanoparticles
KW - targeted therapies
UR - http://www.scopus.com/inward/record.url?scp=85101624969&partnerID=8YFLogxK
U2 - 10.1002/adtp.202000124
DO - 10.1002/adtp.202000124
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AN - SCOPUS:85101624969
SN - 2366-3987
VL - 4
JO - Advanced Therapeutics
JF - Advanced Therapeutics
IS - 1
M1 - 2000124
ER -