Coherent modelling switch between pointwise and distributed representations of cell aggregates (Q515830): Difference between revisions

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The authors consider the set of clones, as aggregates of \(N(t)\) typical particles defined in \(\Omega \subset \mathbb{R}^2\) by the vector \[ X(t)=\{x_1(t),x_2(t),\dots,x_{N(t)}(t),\},\;N(t)\in \mathbb{N} \eqno{(1)} \] with spatial mass density distribution \(\rho(t,y): \mathbb{R}\times \Omega \to \mathbb{R}_+\) such that \[ \int\limits_{\Omega}\rho(t,\mathbf{y})dy=M(t), \; \;\forall t. \eqno{(2)} \] Many additional properties of these clones allow to obtain the system of ODEs (local form of mass balance equation) \[ \frac{dx_j(t)}{dt}=v_L(x_j(t)),\;j=1,\dots,N_L(t), \] \[ \frac{\partial\rho(t,\mathbf{y})}{\partial t}+\nabla\cdot(\rho(t,yv_D(t,y))=\Gamma (t,y), \eqno{(3)} \] where \(x_j\) and \(\rho\) are defined in (1), (2) and \(v_L,\;v_D\) are the velocity of the two cell clones, respectively. Thus the equation (3) represent modeling of clones interaction dynamics -- the model of tumor growth. In conclusion, biologically relevant numerical realizations are presented: they deal with the growth of a tumor spheroid and with the initial differentiation stages of the formation of the zebrafish posterior lateral line. Both phenomena mainly rely on cell phenotypic transition and differentiated behavior, thereby constituting biological systems particularly suitable to assess the advantages of the proposed model.
Property / review text: The authors consider the set of clones, as aggregates of \(N(t)\) typical particles defined in \(\Omega \subset \mathbb{R}^2\) by the vector \[ X(t)=\{x_1(t),x_2(t),\dots,x_{N(t)}(t),\},\;N(t)\in \mathbb{N} \eqno{(1)} \] with spatial mass density distribution \(\rho(t,y): \mathbb{R}\times \Omega \to \mathbb{R}_+\) such that \[ \int\limits_{\Omega}\rho(t,\mathbf{y})dy=M(t), \; \;\forall t. \eqno{(2)} \] Many additional properties of these clones allow to obtain the system of ODEs (local form of mass balance equation) \[ \frac{dx_j(t)}{dt}=v_L(x_j(t)),\;j=1,\dots,N_L(t), \] \[ \frac{\partial\rho(t,\mathbf{y})}{\partial t}+\nabla\cdot(\rho(t,yv_D(t,y))=\Gamma (t,y), \eqno{(3)} \] where \(x_j\) and \(\rho\) are defined in (1), (2) and \(v_L,\;v_D\) are the velocity of the two cell clones, respectively. Thus the equation (3) represent modeling of clones interaction dynamics -- the model of tumor growth. In conclusion, biologically relevant numerical realizations are presented: they deal with the growth of a tumor spheroid and with the initial differentiation stages of the formation of the zebrafish posterior lateral line. Both phenomena mainly rely on cell phenotypic transition and differentiated behavior, thereby constituting biological systems particularly suitable to assess the advantages of the proposed model. / rank
 
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Property / reviewed by
 
Property / reviewed by: Boris Vladimirovich Loginov / rank
 
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Property / Mathematics Subject Classification ID: 35Q70 / rank
 
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Property / Mathematics Subject Classification ID
 
Property / Mathematics Subject Classification ID: 35Q92 / rank
 
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Property / Mathematics Subject Classification ID
 
Property / Mathematics Subject Classification ID: 92C17 / rank
 
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Property / Mathematics Subject Classification ID
 
Property / Mathematics Subject Classification ID: 92C37 / rank
 
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Property / zbMATH DE Number: 6695806 / rank
 
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multiscale modeling
Property / zbMATH Keywords: multiscale modeling / rank
 
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Property / zbMATH Keywords
 
hybrid systems
Property / zbMATH Keywords: hybrid systems / rank
 
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Property / zbMATH Keywords
 
cell differentiation
Property / zbMATH Keywords: cell differentiation / rank
 
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Property / zbMATH Keywords
 
cell phenotypic transition
Property / zbMATH Keywords: cell phenotypic transition / rank
 
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Property / zbMATH Keywords
 
multiscale dynamics
Property / zbMATH Keywords: multiscale dynamics / rank
 
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Revision as of 04:06, 1 July 2023

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Coherent modelling switch between pointwise and distributed representations of cell aggregates
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    Coherent modelling switch between pointwise and distributed representations of cell aggregates (English)
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    17 March 2017
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    The authors consider the set of clones, as aggregates of \(N(t)\) typical particles defined in \(\Omega \subset \mathbb{R}^2\) by the vector \[ X(t)=\{x_1(t),x_2(t),\dots,x_{N(t)}(t),\},\;N(t)\in \mathbb{N} \eqno{(1)} \] with spatial mass density distribution \(\rho(t,y): \mathbb{R}\times \Omega \to \mathbb{R}_+\) such that \[ \int\limits_{\Omega}\rho(t,\mathbf{y})dy=M(t), \; \;\forall t. \eqno{(2)} \] Many additional properties of these clones allow to obtain the system of ODEs (local form of mass balance equation) \[ \frac{dx_j(t)}{dt}=v_L(x_j(t)),\;j=1,\dots,N_L(t), \] \[ \frac{\partial\rho(t,\mathbf{y})}{\partial t}+\nabla\cdot(\rho(t,yv_D(t,y))=\Gamma (t,y), \eqno{(3)} \] where \(x_j\) and \(\rho\) are defined in (1), (2) and \(v_L,\;v_D\) are the velocity of the two cell clones, respectively. Thus the equation (3) represent modeling of clones interaction dynamics -- the model of tumor growth. In conclusion, biologically relevant numerical realizations are presented: they deal with the growth of a tumor spheroid and with the initial differentiation stages of the formation of the zebrafish posterior lateral line. Both phenomena mainly rely on cell phenotypic transition and differentiated behavior, thereby constituting biological systems particularly suitable to assess the advantages of the proposed model.
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    multiscale modeling
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    hybrid systems
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    cell differentiation
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    cell phenotypic transition
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    multiscale dynamics
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