Modeling the effect of p53 on tumor heterogeneity and the mutator phenotype
Author(s) -
Melissa Ryan,
Matthew J. Berryman,
Derek Abbott
Publication year - 2005
Publication title -
proceedings of spie, the international society for optical engineering/proceedings of spie
Language(s) - English
Resource type - Conference proceedings
SCImago Journal Rank - 0.192
H-Index - 176
eISSN - 1996-756X
pISSN - 0277-786X
DOI - 10.1117/12.602423
Subject(s) - phenotype , computer science , genetics , biology , gene
© 2005 COPYRIGHT SPIE--The International Society for Optical Engineeringp53 is an important gene, involved in apoptosis (programmed celldeath), DNA repair, and cell cycle progression. We explore theselective advantages and disadvantages of mutations in the p53 geneon tumor cells, and the heterogeneity of tumor cell populations.Based on an evolutionary computational approach, our model considerschanges in mutation rate caused by lack of DNA repair processes, andthe lack of apoptosis caused by mutations in p53. We find that thedegree of robustness of p53 to mutations has a significant effect onthe tumor heterogeneity and "fitness", with clinical consequencesfor people who inherit p53 mutations.Melissa Ryan, Matthew J. Berryman, and Derek Abbot
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