TY - JOUR
T1 - Glioblastoma
T2 - Current Status, Emerging Targets, and Recent Advances
AU - Thakur, Amandeep
AU - Faujdar, Chetna
AU - Sharma, Ram
AU - Sharma, Sachin
AU - Malik, Basant
AU - Nepali, Kunal
AU - Liou, Jing Ping
N1 - Funding Information:
The corresponding authors are supported by grants from the Ministry of Science and Technology of Taiwan (grant nos. MOST 109-2113-M-038-001, 109-2622-B-038-001, 110-2320-B-038-028, 108-2320-B-038-027-MY3), and 111-2320-B-038-047.
Publisher Copyright:
© 2022 American Chemical Society. All rights reserved.
PY - 2022/7
Y1 - 2022/7
N2 - Glioblastoma (GBM) is a highly malignant brain tumor characterized by a heterogeneous population of genetically unstable and highly infiltrative cells that are resistant to chemotherapy. Although substantial efforts have been invested in the field of anti-GBM drug discovery in the past decade, success has primarily been confined to the preclinical level, and clinical studies have often been hampered due to efficacy-, selectivity-, or physicochemical property-related issues. Thus, expansion of the list of molecular targets coupled with a pragmatic design of new small-molecule inhibitors with central nervous system (CNS)-penetrating ability is required to steer the wheels of anti-GBM drug discovery endeavors. This Perspective presents various aspects of drug discovery (challenges in GBM drug discovery and delivery, therapeutic targets, and agents under clinical investigation). The comprehensively covered sections include the recent medicinal chemistry campaigns embarked upon to validate the potential of numerous enzymes/proteins/receptors as therapeutic targets in GBM.
AB - Glioblastoma (GBM) is a highly malignant brain tumor characterized by a heterogeneous population of genetically unstable and highly infiltrative cells that are resistant to chemotherapy. Although substantial efforts have been invested in the field of anti-GBM drug discovery in the past decade, success has primarily been confined to the preclinical level, and clinical studies have often been hampered due to efficacy-, selectivity-, or physicochemical property-related issues. Thus, expansion of the list of molecular targets coupled with a pragmatic design of new small-molecule inhibitors with central nervous system (CNS)-penetrating ability is required to steer the wheels of anti-GBM drug discovery endeavors. This Perspective presents various aspects of drug discovery (challenges in GBM drug discovery and delivery, therapeutic targets, and agents under clinical investigation). The comprehensively covered sections include the recent medicinal chemistry campaigns embarked upon to validate the potential of numerous enzymes/proteins/receptors as therapeutic targets in GBM.
UR - http://www.scopus.com/inward/record.url?scp=85134434033&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85134434033&partnerID=8YFLogxK
U2 - 10.1021/acs.jmedchem.1c01946
DO - 10.1021/acs.jmedchem.1c01946
M3 - Review article
C2 - 35786935
AN - SCOPUS:85134434033
SN - 0022-2623
VL - 65
SP - 8596
EP - 8685
JO - Journal of Medicinal Chemistry
JF - Journal of Medicinal Chemistry
IS - 13
ER -