TY - JOUR
T1 - G-protein-coupled receptors as therapeutic targets for glioblastoma
AU - Byrne, Kate F.
AU - Pal, Ajay
AU - Curtin, James F.
AU - Stephens, John C.
AU - Kinsella, Gemma K.
N1 - Publisher Copyright:
© 2021 The Author(s)
PY - 2021/12
Y1 - 2021/12
N2 - Glioblastoma multiforme (GBM) is the most common and aggressive primary brain tumour in adults. Treatments include surgical resection, radiotherapy, and chemotherapy. Despite this, the prognosis remains poor, with an impacted quality of life during treatment coupled with brain tumour recurrence; thus, new treatments are desperately needed. In this review, we focus on recent advances in G-protein-coupled receptor (GPCR) targets. To date, the most promising targets are the chemokine, cannabinoid, and dopamine receptors, but future work should further examine the melanocortin receptor-4 (MC4R), adhesion, lysophosphatidic acid (LPA) and smoothened (Smo) receptors to initiate new drug-screening strategies and targeted delivery of safe and effective GBM therapies.
AB - Glioblastoma multiforme (GBM) is the most common and aggressive primary brain tumour in adults. Treatments include surgical resection, radiotherapy, and chemotherapy. Despite this, the prognosis remains poor, with an impacted quality of life during treatment coupled with brain tumour recurrence; thus, new treatments are desperately needed. In this review, we focus on recent advances in G-protein-coupled receptor (GPCR) targets. To date, the most promising targets are the chemokine, cannabinoid, and dopamine receptors, but future work should further examine the melanocortin receptor-4 (MC4R), adhesion, lysophosphatidic acid (LPA) and smoothened (Smo) receptors to initiate new drug-screening strategies and targeted delivery of safe and effective GBM therapies.
KW - G-protein-coupled receptors (GPCRs)
KW - Glioblastoma multiforme (GBM)
UR - http://www.scopus.com/inward/record.url?scp=85111004323&partnerID=8YFLogxK
U2 - 10.1016/j.drudis.2021.07.008
DO - 10.1016/j.drudis.2021.07.008
M3 - Review article
C2 - 34271165
AN - SCOPUS:85111004323
SN - 1359-6446
VL - 26
SP - 2858
EP - 2870
JO - Drug Discovery Today
JF - Drug Discovery Today
IS - 12
ER -