Most human tumors result from the accumulation of multiple genetic and epigenetic alterations in a single cell. Mutations that confer a fitness advantage to the cell are known as driver mutations and are causally related to tumorigenesis. Other mutations, however, do not change the phenotype of the cell or even decrease cellular fitness. While much experimental effort is being devoted to the identification of the functional effects of individual mutations, mathematical modeling of tumor progression generally considers constant fitness increments as mutations are accumulated. In this paper we study a mathematical model of tumor progression with random fitness increments. We analyze a multi-type branching process in which cells accumulate mutations whose fitness effects are chosen from a distribution. We determine the effect of the fitness distribution on the growth kinetics of the tumor. This work contributes to a quantitative understanding of the accumulation of mutations leading to cancer. (C) 2010 Elsevier Inc. All rights reserved.
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Mem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USA
Feinerman, Ofer
Veiga, Joel
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Mem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USA
Veiga, Joel
Dorfman, Jeffrey R.
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Mem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USA
Dorfman, Jeffrey R.
Germain, Ronald N.
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NIAID, Lymphocyte Biol Sect, Immunol Lab, Program Syst Immunol & Infect Dis Modeling,NIH,De, Bethesda, MD 20892 USAMem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USA
Germain, Ronald N.
Altan-Bonnet, Gregoire
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Mem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USA
机构:
Mem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USA
Feinerman, Ofer
Veiga, Joel
论文数: 0引用数: 0
h-index: 0
机构:
Mem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USA
Veiga, Joel
Dorfman, Jeffrey R.
论文数: 0引用数: 0
h-index: 0
机构:
Mem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USA
Dorfman, Jeffrey R.
Germain, Ronald N.
论文数: 0引用数: 0
h-index: 0
机构:
NIAID, Lymphocyte Biol Sect, Immunol Lab, Program Syst Immunol & Infect Dis Modeling,NIH,De, Bethesda, MD 20892 USAMem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USA
Germain, Ronald N.
Altan-Bonnet, Gregoire
论文数: 0引用数: 0
h-index: 0
机构:
Mem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USAMem Sloan Kettering Canc Ctr, ImmunoDynam Grp, Program Computat Biol & Immunol, New York, NY 10065 USA