| Literature DB >> 24333720 |
Bérengère Gobin1, Séverine Battaglia1, Rachel Lanel1, Julie Chesneau1, Jérôme Amiaud1, Françoise Rédini2, Benjamin Ory1, Dominique Heymann3.
Abstract
Despite recent improvements in chemotherapy and surgery, the problem of non-response osteosarcoma to chemotherapy remains, and is a parameter that is critical for prognosis. The present work investigated the therapeutic value of NVP-BEZ235, a dual class I PI3K/mTOR inhibitor. NVP-BEZ235 inhibited osteosarcoma cell proliferation by inducing G0/G1 cell cycle arrest with no caspase activation. In murine pre-clinical models, NVP-BEZ235 significantly slowed down tumor progression and ectopic tumor bone formation with decreased numbers of Ki67(+) cells and reduced tumor vasculature. Finally, NVP-BEZ235 considerably improved the survival rate of mice with osteosarcoma. Taken together, the results of the present work show that NVP-BEZ235 exhibits therapeutic interest in osteosarcoma and may be a promising adjuvant drug for bone sarcomas.Entities:
Keywords: Osteosarcoma; PI3K Inhibitor; Pre-clinical model; Survival rate; mTOR Inhibitor
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Year: 2013 PMID: 24333720 DOI: 10.1016/j.canlet.2013.11.017
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679