Dynamics of metastasis suppressor gene inactivation

Franziska Michor, Yoh Iwasa

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

For most cancer cell types, the acquisition of metastatic ability leads to clinically incurable disease. Twelve metastasis suppressor genes (MSGs) have been identified that reduce the metastatic propensity of cancer cells. If these genes are inactivated in both alleles, metastatic ability is promoted. Here, we develop a mathematical model of the dynamics of MSG inactivation and calculate the expected number of metastases formed by a tumor. We analyse the effects of increased mutation rates and different fitness values of cells with one or two inactivated alleles on the ability of a tumor to form metastases. We find that mutations that are negatively selected in the main tumor are unlikely to be responsible for the majority of metastases produced by a tumor. Most metastases-causing mutations will be present in all (or most) cells in the main tumor.

Original languageEnglish
Pages (from-to)676-689
Number of pages14
JournalJournal of Theoretical Biology
Volume241
Issue number3
DOIs
Publication statusPublished - Jul 7 2006

Fingerprint

tumor suppressor genes
Metastasis
Gene Silencing
Tumor Suppressor Genes
Tumors
inactivation
Genes
metastasis
Tumor
Gene
neoplasms
Neoplasms
Mutation
mutation
Neoplasm Metastasis
Cell
Cells
Cancer
alleles
Alleles

All Science Journal Classification (ASJC) codes

  • Statistics and Probability
  • Modelling and Simulation
  • Biochemistry, Genetics and Molecular Biology(all)
  • Immunology and Microbiology(all)
  • Agricultural and Biological Sciences(all)
  • Applied Mathematics

Cite this

Dynamics of metastasis suppressor gene inactivation. / Michor, Franziska; Iwasa, Yoh.

In: Journal of Theoretical Biology, Vol. 241, No. 3, 07.07.2006, p. 676-689.

Research output: Contribution to journalArticle

Michor, Franziska ; Iwasa, Yoh. / Dynamics of metastasis suppressor gene inactivation. In: Journal of Theoretical Biology. 2006 ; Vol. 241, No. 3. pp. 676-689.
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