This feature is a main obstacle to effectiveness of chemotherapy against HCC

This feature is a main obstacle to effectiveness of chemotherapy against HCC

in 6, a mediator of chronic inflammation that is increased in the central nervous system of AD individuals. In addition, Bath et al. observed a strong expression correlation between IL-6 and the mitogen activated protein kinase 14 that is an important regulator of cell cycle checkpoints. IL-6 in pre-senescent and senescent astrocytes could be abolished by drug inhibition of p38MAPK. These experimental results suggest that astrocyte senescence is strongly connected to p38MAPK activation. However, the exact molecular mechanisms that drive astrocytes into senescence remain obscure. p38MAPK can induce checkpoint arrest and its overexpression induces senescence in fibroblasts which are cells that share get AEB-071 functional similarities with astrocytes. Based on a previous, specific model of senescence onset at G1/S checkpoint, in this work we propose that p38MAPK induction can explain astrocyte senescence and SASP and we propose an extended logical model of the process integrating checkpoints G1/S and G2/M as both have similar mechanisms of checkpoint activation by p38MAPK upon DNA damage. The model corroborates several experimental findings and make some predictions. In what follows we describe the organization of the paper. The logical modeling method is described in the next section. Then after an overview of general molecular mechanisms of checkpoint and cell fate decisions, our model is defined and studied in the Results section. The Discussion section summarizes the implications of this work and indicates future work. Methods Logical models were used to study cell cycle control and cell fate decisions, for a review see. A logical model is defined by a directed regulatory graph where discrete variables are associated with the nodes and logical rules determine the evolution of these variables. Nodes in this type of graph symbolize molecular components as genes and/or proteins, PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/19777101 biological processes or phenomenological events. Edges represent activatory or inhibitory effects and variables denote activity levels with two or more states. In most cases the variables are Boolean, but multi-valued variables can represent different influences of a node affecting its targets. The evolution of the level of each component is defined by a logical rule subjected to the regulators of this component. Input components are not regulated and symbolize extrinsic constant PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/19778700 conditions. The dynamics of logical models can be characterized in terms of state transition graphs, where the states are nodes comprising the level of each component in the model and the edges, connecting the nodes, represent state transitions resulting from the logical rules that change the levels of the model components. End nodes in state transition graphs correspond to attractors that can be a stable state or a cycle. The logical framework allows the consideration of diverse molecular processes associated with different time scales in a unique model as it happens with transcriptional regulation and 2 / 12 A Model for p38MAPK-Induced Astrocyte Senescence protein phosphorylation. In addition, the logical method permits analysis of perturbations consisting in retaining a variable to its lowest levels, known as loss of function experiment, or to its positive levels, known as gain of function experiment. This framework is implemented in the tool GINsim, which permits different types of analysis of logical models including the determination of stable states. Results Cell fate decisions between apopto

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