Sharp2019 - AML

  public model
Model Identifier
BIOMD0000000798
Short description
The paper describes a model of acute myeloid leukaemia. Created by COPASI 4.26 (Build 213) This model is described in the article: Optimal control of acute myeloid leukaemia Jesse A. Sharp, Alexander P Browning, Tarunendu Mapder, Kevin Burrage, Matthew J Simpson Journal of Theoretical Biology 470 (2019) 30–42 Abstract: Acute myeloid leukaemia (AML) is a blood cancer affecting haematopoietic stem cells. AML is routinely treated with chemotherapy, and so it is of great interest to develop optimal chemotherapy treatment strategies. In this work, we incorporate an immune response into a stem cell model of AML, since we find that previous models lacking an immune response are inappropriate for deriving optimal control strategies. Using optimal control theory, we produce continuous controls and bang-bang controls, corre- sponding to a range of objectives and parameter choices. Through example calculations, we provide a practical approach to applying optimal control using Pontryagin’s Maximum Principle. In particular, we describe and explore factors that have a profound influence on numerical convergence. We find that the convergence behaviour is sensitive to the method of control updating, the nature of the control, and to the relative weighting of terms in the objective function. All codes we use to implement optimal control are made available. 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
  • Optimal control of acute myeloid leukaemia.
  • Sharp JA, Browning AP, Mapder T, Burrage K, Simpson MJ
  • Journal of theoretical biology , 6/ 2019 , Volume 470 , pages: 30-42 , PubMed ID: 30853393
  • School of Mathematical Sciences, Queensland University of Technology (QUT), Australia; ARC Centre of Excellence for Mathematical and Statistical Frontiers, QUT, Australia.
  • Acute myeloid leukaemia (AML) is a blood cancer affecting haematopoietic stem cells. AML is routinely treated with chemotherapy, and so it is of great interest to develop optimal chemotherapy treatment strategies. In this work, we incorporate an immune response into a stem cell model of AML, since we find that previous models lacking an immune response are inappropriate for deriving optimal control strategies. Using optimal control theory, we produce continuous controls and bang-bang controls, corresponding to a range of objectives and parameter choices. Through example calculations, we provide a practical approach to applying optimal control using Pontryagin's Maximum Principle. In particular, we describe and explore factors that have a profound influence on numerical convergence. We find that the convergence behaviour is sensitive to the method of control updating, the nature of the control, and to the relative weighting of terms in the objective function. All codes we use to implement optimal control are made available.
Contributors
Submitter of the first revision: Jinghao Men
Submitter of this revision: Jinghao Men
Modellers: Jinghao Men

Metadata information

is (2 statements)
BioModels Database BIOMD0000000798
BioModels Database MODEL1908190001

isDescribedBy (1 statement)
PubMed 30853393

hasTaxon (1 statement)
Taxonomy Homo sapiens

hasProperty (2 statements)
Mathematical Modelling Ontology Ordinary differential equation model
Experimental Factor Ontology acute myeloid leukemia


Curation status
Curated



Connected external resources

SBGN view in Newt Editor

Name Description Size Actions

Model files

Sharp2019.xml SBML L3V1 representation of AML model 55.82 KB Preview | Download

Additional files

Sharp2019.cps CPS file of the model in COPASI 74.86 KB Preview | Download
Sharp2019.sedml Auto-generated SEDML file 3.58 KB Preview | Download

  • Model originally submitted by : Jinghao Men
  • Submitted: Aug 19, 2019 10:41:23 AM
  • Last Modified: Aug 19, 2019 10:41:23 AM
Revisions
  • Version: 3 public model Download this version
    • Submitted on: Aug 19, 2019 10:41:23 AM
    • Submitted by: Jinghao Men
    • With comment: Automatically added model identifier BIOMD0000000798
Legends
: Variable used inside SBML models


Species
Species Initial Concentration/Amount
S

hematopoietic stem cell
0.1 mmol
A

common myeloid progenitor
0.0 mmol
T

lymphoma or leukaemia cell line
0.0 mmol
L

stem cell
0.1 mmol
Reactions
Reactions Rate Parameters
S => A bone_marrow*ds*S ds = 0.14 1
=> S bone_marrow*ps*S*(k1-Z1) k1 = 1.0 1; Z1 = 0.1 1; ps = 0.5 1
T => bone_marrow*ut*T ut = 0.3 1
L => T bone_marrow*dl*L dl = 0.05 1
L => bone_marrow*a*L/(y+L) y = 0.01 1; a = 0.015 1
=> L bone_marrow*pl*L*(k2-Z2) pl = 0.27 1; k2 = 1.0 1; Z2 = 0.1 1
=> A bone_marrow*pa*A*(k2-Z2) pa = 0.43 1; k2 = 1.0 1; Z2 = 0.1 1
A => D bone_marrow*da*A da = 0.44 1
Curator's comment:
(added: 19 Aug 2019, 10:41:15, updated: 19 Aug 2019, 10:41:15)
Publication figure 2 reproduced as per literature. Figure data is generated using COPASI 4.26 (build 213).