Monro2008 - chemotherapy resistance

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.
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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
Submitter of this revision: Jinghao Men
Modellers: Jinghao Men
Metadata information
is (2 statements)
isDescribedBy (1 statement)
hasTaxon (1 statement)
hasProperty (2 statements)
isDescribedBy (1 statement)
hasTaxon (1 statement)
hasProperty (2 statements)
Curation status
Curated
Modelling approach(es)
Tags
Connected external resources
Name | Description | Size | Actions |
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Model files |
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Monro2008.xml | SBML L3V1 representation of chemotherapy resistance model | 34.89 KB | Preview | Download |
Additional files |
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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
Legends
: Variable used inside SBML models
: 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)
(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).