| Literature DB >> 25217522 |
Chiara Ambrogio1, Francisco J Carmona2, August Vidal3, Mattia Falcone4, Patricia Nieto1, Octavio A Romero2, Sara Puertas5, Miguel Vizoso5, Ernest Nadal6, Teresa Poggio7, Montserrat Sánchez-Céspedes2, Manel Esteller8, Francisca Mulero9, Claudia Voena7, Roberto Chiarle10, Mariano Barbacid1, David Santamaría11, Alberto Villanueva12.
Abstract
Cancer evolution is a process that is still poorly understood because of the lack of versatile in vivo longitudinal studies. By generating murine non-small cell lung cancer (NSCLC) orthoallobanks and paired primary cell lines, we provide a detailed description of an in vivo, time-dependent cancer malignization process. We identify the acquisition of metastatic dissemination potential, the selection of co-driver mutations, and the appearance of naturally occurring intratumor heterogeneity, thus recapitulating the stochastic nature of human cancer development. This approach combines the robustness of genetically engineered cancer models with the flexibility of allograft methodology. We have applied this tool for the preclinical evaluation of therapeutic approaches. This system can be implemented to improve the design of future treatments for patients with NSCLC. ©2014 American Association for Cancer Research.Entities:
Mesh:
Year: 2014 PMID: 25217522 DOI: 10.1158/0008-5472.CAN-14-1606
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701