mTOR Pathway and mTOR Inhibitors in Head and Neck Cancer
Author(s) -
Wei Gao,
Zeng-Hong Li,
Jimmy Yu Wai Chan,
Wai Kuen Ho,
ThianSze Wong
Publication year - 2012
Publication title -
isrn otolaryngology
Language(s) - English
Resource type - Journals
eISSN - 2090-5750
pISSN - 2090-5742
DOI - 10.5402/2012/953089
Subject(s) - everolimus , pi3k/akt/mtor pathway , temsirolimus , medicine , head and neck cancer , cancer , cancer research , targeted therapy , radiation therapy , oncology , p70 s6 kinase 1 , discovery and development of mtor inhibitors , signal transduction , biology , biochemistry
Head and neck cancer is the sixth most common type of Cancer worldwide. Since conventional treatment regimens are nonselective and are associated with systemic toxicities, intense investigations focus on molecular targeted therapy with high selectivity and low adverse effects. mTOR signaling pathway has been found to be activated in head and neck cancer, making it attractive for targeted therapy. In addition, expression levels of mTOR and downstream targets eIF4E, 4EBP1, S6K1, and S6 are potential diagnostic and prognostic biomarkers for head and neck cancer. mTOR inhibitors, such as rapamycin and its derivatives temsirolimus and everolimus, exhibit inhibitory effects on head and neck cancer in both in vitro cell line model and in vivo xenograft model. A large number of clinical trials have been initiated to evaluate the therapeutic effects of mTOR inhibitors on patients with head and neck cancer. mTOR inhibitor has potential as a single therapeutic agent or in combination with radiation, chemotherapeutic agents, or other targeted therapeutic agents to obtain synergistic repression on head and neck cancer.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom