Literature DB >> 8186758

Time-continuous branching walk models of unstable gene amplification.

M Kimmel1, D N Stivers.   

Abstract

We consider a stochastic mechanism of the loss of resistance of cancer cells to cytotoxic agents, in terms of unstable gene amplification. Two models being different versions of a time-continuous branching random walk are presented. Both models assume strong dependence in replication and segregation of the extrachromosomal elements. The mathematical part of the paper includes the expression for the expected number of cells with a given number of gene copies in terms of modified Bessel functions. This adds to the collection of rare explicit solutions to branching process models. Original asymptotic expansions are also demonstrated. Fitting the model to experimental data yields estimates of the probabilities of gene amplification and deamplification. The thesis of the paper is that purely stochastic mechanisms may explain the dynamics of reversible drug resistance of cancer cells. Various stochastic approaches and their limitations are discussed.

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Year:  1994        PMID: 8186758     DOI: 10.1007/bf02460646

Source DB:  PubMed          Journal:  Bull Math Biol        ISSN: 0092-8240            Impact factor:   1.758


  25 in total

Review 1.  The importance of circular DNA in mammalian gene amplification.

Authors:  G M Wahl
Journal:  Cancer Res       Date:  1989-03-15       Impact factor: 12.701

2.  Evolution of repeated DNA sequences by unequal crossover.

Authors:  G P Smith
Journal:  Science       Date:  1976-02-13       Impact factor: 47.728

3.  The dynamics of gene amplification described as a multitype compartmental model and as a branching process.

Authors:  L E Harnevo; Z Agur
Journal:  Math Biosci       Date:  1991-02       Impact factor: 2.144

Review 4.  Gene amplification in cultured cells.

Authors:  R T Schimke
Journal:  J Biol Chem       Date:  1988-05-05       Impact factor: 5.157

5.  Some stochastic models for plasmid copy number.

Authors:  E Seneta; S Tavaré
Journal:  Theor Popul Biol       Date:  1983-04       Impact factor: 1.570

6.  Analysis of variability in albumin content of sister hepatoma cells and a model for geometric phenotypic variability (quantitative shift model).

Authors:  J A Peterson
Journal:  Somat Cell Mol Genet       Date:  1984-07

7.  Effects of segregation and selection on instability of plasmid pACYC184 in Escherichia coli B.

Authors:  R E Lenski; J E Bouma
Journal:  J Bacteriol       Date:  1987-11       Impact factor: 3.490

8.  A branching process model of gene amplification following chromosome breakage.

Authors:  M Kimmel; D E Axelrod; G M Wahl
Journal:  Mutat Res       Date:  1992-05       Impact factor: 2.433

9.  Drug resistance as a dynamic process in a model for multistep gene amplification under various levels of selection stringency.

Authors:  L E Harnevo; Z Agur
Journal:  Cancer Chemother Pharmacol       Date:  1992       Impact factor: 3.333

10.  Loss and stabilization of amplified dihydrofolate reductase genes in mouse sarcoma S-180 cell lines.

Authors:  R J Kaufman; P C Brown; R T Schimke
Journal:  Mol Cell Biol       Date:  1981-12       Impact factor: 4.272

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  2 in total

Review 1.  Mathematical modeling as a tool for planning anticancer therapy.

Authors:  Andrzej Swierniak; Marek Kimmel; Jaroslaw Smieja
Journal:  Eur J Pharmacol       Date:  2009-10-13       Impact factor: 4.432

2.  Optimizing combination therapies with existing and future CML drugs.

Authors:  Allen A Katouli; Natalia L Komarova
Journal:  PLoS One       Date:  2010-08-23       Impact factor: 3.240

  2 in total

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