| Literature DB >> 28450157 |
Hiroaki Miyahara1, Sridevi Yadavilli2, Manabu Natsumeda1, Jeffrey A Rubens3, Louis Rodgers4, Madhuri Kambhampati2, Isabella C Taylor3, Harpreet Kaur3, Laura Asnaghi1, Charles G Eberhart1, Katherine E Warren4, Javad Nazarian5, Eric H Raabe6.
Abstract
Diffuse intrinsic pontine glioma (DIPG) is an invasive and treatment-refractory pediatric brain tumor. Primary DIPG tumors harbor a number of mutations including alterations in PTEN, AKT, and PI3K and exhibit activation of mammalian Target of Rapamycin Complex 1 and 2 (mTORC1/2). mTORC1/2 regulate protein translation, cell growth, survival, invasion, and metabolism. Pharmacological inhibition of mTORC1 is minimally effective in DIPG. However, the activity of dual TORC kinase inhibitors has not been examined in this tumor type. Nanomolar levels of the mTORC1/2 inhibitor TAK228 reduced expression of p-AKTS473 and p-S6S240/244 and suppressed the growth of DIPG lines JHH-DIPG1, SF7761, and SU-DIPG-XIII. TAK228 induced apoptosis in DIPG cells and cooperated with radiation to further block proliferation and enhance apoptosis. TAK228 monotherapy inhibited the tumorigenicity of a murine orthotopic model of DIPG, more than doubling median survival (p = 0.0017) versus vehicle. We conclude that dual mTOR inhibition is a promising potential candidate for DIPG treatment.Entities:
Keywords: INK128; MLN0128; Pediatric brain tumor; Sapanisertib; mTOR
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Year: 2017 PMID: 28450157 PMCID: PMC5569904 DOI: 10.1016/j.canlet.2017.04.019
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 9.756