Monro2008 - chemotherapy resistance

  public model
Model Identifier
BIOMD0000000776
Short description
The paper describes a model of resistance of cancer to chemotherapy. Created by COPASI 4.25 (Build 207) This model is described in the article: Modelling chemotherapy resistance in palliation and failed cure Helen C. Monro, Eamonn A. Gaffney J Theor Biol. 2009, 257 (2), pp.292 Abstract: The goal of palliative cancer chemotherapy treatment is to prolong survival and improve quality of life when tumour eradication is not feasible. Chemotherapy protocol design is considered in this context using a simple, robust, model of advanced tumour growth with Gompertzian dynamics, taking into account the effects of drug resistance. It is predicted that reduced chemotherapy protocols can readily lead to improved survival times due to the effects of competition between resistant and sensitive tumour cells. Very early palliation is also predicted to quickly yield near total tumour resistance and thus decrease survival duration. Finally, our simulations indicate that failed curative attempts using dose densification, a common protocol escalation strategy, can reduce survival times. To cite BioModels Database, please use: BioModels Database: An enhanced, curated and annotated resource for published quantitative kinetic models . To the extent possible under law, all copyright and related or neighbouring rights to this encoded model have been dedicated to the public domain worldwide. Please refer to CC0 Public Domain Dedication for more information.
Format
SBML (L3V1)
Related Publication
  • Modelling chemotherapy resistance in palliation and failed cure.
  • Monro HC, Gaffney EA
  • Journal of theoretical biology , 3/ 2009 , Volume 257 , Issue 2 , pages: 292-302 , PubMed ID: 19135065
  • University of Birmingham, Edgbaston, UK. monro@mat.bham.ac.uk
  • The goal of palliative cancer chemotherapy treatment is to prolong survival and improve quality of life when tumour eradication is not feasible. Chemotherapy protocol design is considered in this context using a simple, robust, model of advanced tumour growth with Gompertzian dynamics, taking into account the effects of drug resistance. It is predicted that reduced chemotherapy protocols can readily lead to improved survival times due to the effects of competition between resistant and sensitive tumour cells. Very early palliation is also predicted to quickly yield near total tumour resistance and thus decrease survival duration. Finally, our simulations indicate that failed curative attempts using dose densification, a common protocol escalation strategy, can reduce survival times.
Contributors
Submitter of the first revision: Jinghao Men
Submitter of this revision: Jinghao Men
Modellers: Jinghao Men

Metadata information

is (2 statements)
BioModels Database BIOMD0000000776
BioModels Database MODEL1908020002

isDescribedBy (1 statement)
PubMed 19135065

hasTaxon (1 statement)
Taxonomy Homo sapiens

hasProperty (2 statements)
Mathematical Modelling Ontology Ordinary differential equation model
NCIt Chemotherapy


Curation status
Curated


Tags

Connected external resources

SBGN view in Newt Editor

Name Description Size Actions

Model files

Monro2008.xml SBML L3V1 representation of chemotherapy resistance model 34.89 KB Preview | Download

Additional files

Monro2008.cps CPS file of the model in COPASI 57.54 KB Preview | Download
Monro2008.sedml Auto-generated SEDML file 3.15 KB Preview | Download

  • Model originally submitted by : Jinghao Men
  • Submitted: Aug 2, 2019 4:44:25 PM
  • Last Modified: Aug 2, 2019 4:44:25 PM
Revisions
  • Version: 3 public model Download this version
    • Submitted on: Aug 2, 2019 4:44:25 PM
    • Submitted by: Jinghao Men
    • With comment: Automatically added model identifier BIOMD0000000776
Legends
: Variable used inside SBML models


Species
Species Initial Concentration/Amount
S

malignant cell
1.0E10 mmol
R

malignant cell
200000.0 mmol
Reactions
Reactions Rate Parameters
S => R tme*(-b)*ln(N/Ninf)*(t1*S-t2*R) N = 1.00002E10 1; Ninf = 2.0E12 1; t1 = 1.0E-6 1; t2 = 1.0E-6 1; b = 0.005928 1/d
=> S tme*(-b)*ln(N/Ninf)*S N = 1.00002E10 1; Ninf = 2.0E12 1; b = 0.005928 1/d
=> R tme*(-b)*ln(N/Ninf)*R N = 1.00002E10 1; Ninf = 2.0E12 1; b = 0.005928 1/d
S => tme*(-b)*ln(N/Ninf)*C0*S N = 1.00002E10 1; Ninf = 2.0E12 1; b = 0.005928 1/d; C0 = 2.0 1
Curator's comment:
(added: 02 Aug 2019, 16:44:12, updated: 02 Aug 2019, 16:44:12)
Publication figure 2 reproduced as per literature. Figure data is generated using COPASI 4.25 (build 197).