Should tissue structure suppress or amplify selection to minimize cancer risk?
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Arne Traulsen | Benjamin Werner | Laura Hindersin | David Dingli | A. Traulsen | D. Dingli | B. Werner | Laura Hindersin
[1] R. Durrett,et al. Evolutionary dynamics of tumor progression with random fitness values. , 2010, Theoretical population biology.
[2] Arne Traulsen,et al. The effect of population structure on the rate of evolution , 2013, Proceedings of the Royal Society B: Biological Sciences.
[3] Alexander G. Fletcher,et al. Quantification of Crypt and Stem Cell Evolution in the Normal and Neoplastic Human Colon , 2014, Cell reports.
[4] H. Ohtsuki,et al. Accumulation of driver and passenger mutations during tumor progression , 2009, Proceedings of the National Academy of Sciences.
[5] R. Kassen,et al. Distribution of fitness effects among beneficial mutations before selection in experimental populations of bacteria , 2006, Nature Genetics.
[6] Nicholas A. Wright,et al. The biology of epithelial cell populations , 1984 .
[7] D. Hanahan,et al. Hallmarks of Cancer: The Next Generation , 2011, Cell.
[8] Steven A Frank,et al. Stochastic elimination of cancer cells , 2003, Proceedings of the Royal Society of London. Series B: Biological Sciences.
[9] Arne Traulsen,et al. Somatic mutations and the hierarchy of hematopoiesis , 2010, BioEssays : news and reviews in molecular, cellular and developmental biology.
[10] Tom Lenaerts,et al. Dynamics of Mutant Cells in Hierarchical Organized Tissues , 2011, PLoS Comput. Biol..
[11] Charles M. Grinstead,et al. Introduction to probability , 1999, Statistics for the Behavioural Sciences.
[12] J. Krug,et al. Clonal interference in large populations , 2007, Proceedings of the National Academy of Sciences.
[13] D. Hanahan,et al. The Hallmarks of Cancer , 2000, Cell.
[14] Ignacio A. Rodriguez-Brenes,et al. Minimizing the risk of cancer: tissue architecture and cellular replication limits , 2013, Journal of The Royal Society Interface.
[15] Natalia L. Komarova,et al. The duality of spatial death–birth and birth–death processes and limitations of the isothermal theorem , 2014, Royal Society Open Science.
[16] Shane T. Jensen,et al. Potential Mechanisms for Cancer Resistance in Elephants and Comparative Cellular Response to DNA Damage in Humans. , 2015, JAMA.
[17] Martin A. Nowak,et al. Evolutionary dynamics on graphs , 2005, Nature.
[18] Arne Traulsen,et al. Counterintuitive properties of the fixation time in network-structured populations , 2014, Journal of The Royal Society Interface.
[19] Krishnendu Chatterjee,et al. Amplifiers of selection , 2015, Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences.
[20] J. Kingman. A FIRST COURSE IN STOCHASTIC PROCESSES , 1967 .
[21] C. Höög,et al. Merotelic attachments allow alignment and stabilization of chromatids in meiosis II oocytes , 2014, Nature Communications.
[22] Arne Traulsen,et al. Cancer initiation with epistatic interactions between driver and passenger mutations. , 2013, Journal of theoretical biology.
[23] N. Komarova,et al. Epithelial tissue architecture protects against cancer. , 2006, Mathematical biosciences.
[24] Benjamin J. Raphael,et al. Mutational landscape and significance across 12 major cancer types , 2013, Nature.
[25] M. Hochberg,et al. Peto's paradox and human cancers , 2015, Philosophical Transactions of the Royal Society B: Biological Sciences.
[26] J. DeGregori,et al. Stochastic modeling reveals an evolutionary mechanism underlying elevated rates of childhood leukemia , 2016, Proceedings of the National Academy of Sciences.
[27] K. Kinzler,et al. Cancer genes and the pathways they control , 2004, Nature Medicine.
[28] R. Watson,et al. PERSPECTIVE: SIGN EPISTASIS AND GENETIC COSTRAINT ON EVOLUTIONARY TRAJECTORIES , 2005, Evolution; international journal of organic evolution.
[29] C. Zeyl,et al. Estimates of the rate and distribution of fitness effects of spontaneous mutation in Saccharomyces cerevisiae. , 2001, Genetics.
[30] M. Nowak,et al. The linear process of somatic evolution , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[31] Andrea Sottoriva,et al. Defining Stem Cell Dynamics in Models of Intestinal Tumor Initiation , 2013, Science.
[32] Allon M Klein,et al. Intestinal Stem Cell Replacement Follows a Pattern of Neutral Drift , 2010, Science.
[33] C. Maley,et al. Spatial structure increases the waiting time for cancer , 2011, New journal of physics.
[34] B. Vogelstein,et al. A genetic model for colorectal tumorigenesis , 1990, Cell.
[35] John N. Tsitsiklis,et al. Introduction to Probability , 2002 .
[36] Andrea Sottoriva,et al. Cancer Evolution and the Limits of Predictability in Precision Cancer Medicine , 2016, Trends in cancer.
[37] C. Hauert,et al. Social evolution in structured populations , 2014, Nature Communications.
[38] Louis Vermeulen,et al. Stem cell dynamics in homeostasis and cancer of the intestine , 2014, Nature Reviews Cancer.
[39] Arne Traulsen,et al. Exact numerical calculation of fixation probability and time on graphs , 2015, Biosyst..
[40] Martin A. Nowak,et al. Genetic Progression and the Waiting Time to Cancer , 2007, PLoS Comput. Biol..
[41] B. Vogelstein,et al. Variation in cancer risk among tissues can be explained by the number of stem cell divisions , 2015, Science.
[42] L. Wahl,et al. The Effects of Population Bottlenecks on Clonal Interference, and the Adaptation Effective Population Size , 2009, Evolution; international journal of organic evolution.
[43] P. Keightley,et al. A Comparison of Models to Infer the Distribution of Fitness Effects of New Mutations , 2013, Genetics.
[44] Tim Holland-Letz,et al. Fundamental properties of unperturbed haematopoiesis from stem cells in vivo , 2015, Nature.
[45] A. Eyre-Walker,et al. The Distribution of Fitness Effects of New Deleterious Amino Acid Mutations in Humans , 2006, Genetics.
[46] Martin A. Nowak,et al. The Molecular Clock of Neutral Evolution Can Be Accelerated or Slowed by Asymmetric Spatial Structure , 2014, PLoS Comput. Biol..
[47] Martin A. Nowak,et al. Universality of fixation probabilities in randomly structured populations , 2014, Scientific Reports.
[48] Daniel J. Gaffney,et al. Quantifying the slightly deleterious mutation model of molecular evolution. , 2002, Molecular biology and evolution.
[49] Michael Doebeli,et al. Consolidating Birth-Death and Death-Birth Processes in Structured Populations , 2013, PloS one.
[50] S. Elena,et al. The causes of epistasis , 2011, Proceedings of the Royal Society B: Biological Sciences.
[51] Arne Traulsen,et al. Most Undirected Random Graphs Are Amplifiers of Selection for Birth-Death Dynamics, but Suppressors of Selection for Death-Birth Dynamics , 2015, PLoS Comput. Biol..
[52] R. Lenski,et al. Negative Epistasis Between Beneficial Mutations in an Evolving Bacterial Population , 2011, Science.
[53] Samuel Karlin,et al. A First Course on Stochastic Processes , 1968 .
[54] T. Brümmendorf,et al. Reconstructing the in vivo dynamics of hematopoietic stem cells from telomere length distributions , 2015, eLife.
[55] L. Hurst. Epistasis and the Evolutionary Process , 2000, Heredity.
[56] M. Nowak,et al. Unwanted Evolution , 2013, Science.
[57] H. Girardey,et al. Trajectories , 2009, Handbook of Critical Agrarian Studies.
[58] Arne Traulsen,et al. Ontogenic growth as the root of fundamental differences between childhood and adult cancer , 2016, Stem cells.
[59] R. Axelrod,et al. Evolutionary Dynamics , 2004 .