TY - JOUR
T1 - Vestibular Schwannoma Drug Development
T2 - Current State-of-the Art
AU - Miller, Craig
AU - Sudhoff, Holger
AU - Jacob, Abraham
N1 - Publisher Copyright:
© 2014, Springer Science+Business Media New York.
PY - 2014/12
Y1 - 2014/12
N2 - Vestibular schwannomas (VS) can cause significant patient morbidity. Currently, surgery and stereotactic radiation therapy are available treatment options. Recent breakthroughs in research have discovered key cell surface receptors and intracellular signaling pathways that drive vestibular schwannoma tumorigenesis, proliferation, and survival. A number of promising inhibitors targeting these signaling molecules have also now shown efficacy in preclinical VS cell culture models and animal experiments, with some recently entering human clinical trials. In this review, we summarize ErbB receptor signaling, PDGF receptors, MAP kinase signaling, AKT, p21-activated kinase signaling, mTOR, and VEGF signaling in the context of vestibular schwannoma drug development and medical treatment.
AB - Vestibular schwannomas (VS) can cause significant patient morbidity. Currently, surgery and stereotactic radiation therapy are available treatment options. Recent breakthroughs in research have discovered key cell surface receptors and intracellular signaling pathways that drive vestibular schwannoma tumorigenesis, proliferation, and survival. A number of promising inhibitors targeting these signaling molecules have also now shown efficacy in preclinical VS cell culture models and animal experiments, with some recently entering human clinical trials. In this review, we summarize ErbB receptor signaling, PDGF receptors, MAP kinase signaling, AKT, p21-activated kinase signaling, mTOR, and VEGF signaling in the context of vestibular schwannoma drug development and medical treatment.
KW - AKT
KW - mTOR
KW - Neurofibromatosis type II
KW - NF2
KW - PAK
KW - Vestibular schwannomas
UR - http://www.scopus.com/inward/record.url?scp=84971256384&partnerID=8YFLogxK
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U2 - 10.1007/s40136-014-0063-8
DO - 10.1007/s40136-014-0063-8
M3 - Review article
AN - SCOPUS:84971256384
VL - 2
SP - 217
EP - 225
JO - Current Otorhinolaryngology Reports
JF - Current Otorhinolaryngology Reports
SN - 2167-583X
IS - 4
ER -