senescent cells in growing tumors population dynamics and cancer stem cells衰老细胞在肿瘤增长种群动态和癌症干细胞.pdfVIP

Senescent Cells in Growing Tumors: Population Dynamics and Cancer Stem Cells 1 2,3 4 Caterina A. M. La Porta , Stefano Zapperi *, James P. Sethna 1 Department of Biomolecular Science and Biotechnology, University of Milano, Milano, Italy, 2 CNR-IENI, Milano, Italy, 3 ISI Foundation, Torino, Italy, 4 LASSP, Department of Physics, Cornell University, Ithaca, New York, United States of America Abstract Tumors are defined by their intense proliferation, but sometimes cancer cells turn senescent and stop replicating. In the stochastic cancer model in which all cells are tumorigenic, senescence is seen as the result of random mutations, suggesting that it could represent a barrier to tumor growth. In the hierarchical cancer model a subset of the cells, the cancer stem cells, divide indefinitely while other cells eventually turn senescent. Here we formulate cancer growth in mathematical terms and obtain predictions for the evolution of senescence. We perform experiments in human melanoma cells which are compatible with the hierarchical model and show that senescence is a reversible process controlled by survivin. We conclude that enhancing senescence is unlikely to provide a useful therapeutic strategy to fight cancer, unless the cancer stem cells are specifically targeted. Citation: La Porta CAM, Zapperi S, Sethna JP (2012) Senescent Cells in Growing Tumors: Population Dynamics and Cancer Stem Cells. PLoS Comput Biol 8(1): e1002316. doi:10.1371/journal.pcbi.1002316 Editor: Eytan Domany, Weizmann Institute of Science, Israel Received July 25, 2011; Accepted November 2, 2011; Published January 19, 2012 Copyright: 2012 La Porta et al. This is an open-access article distributed under the terms of t