Session

Mathematical models of cell motility and cancer progression in microenvironment: design, experiments, mathematical framework, and hypothesis test

12 Jul 2018, 10:30
New Law School/--024 (University of Sydney)

New Law School/--024

University of Sydney

100

Conveners

Mathematical models of cell motility and cancer progression in microenvironment: design, experiments, mathematical framework, and hypothesis test: Part A

  • Hans Othmer ()
  • Yanjin Kim (Konkuk University)

Mathematical models of cell motility and cancer progression in microenvironment: design, experiments, mathematical framework, and hypothesis test: Part B

  • Yangjin Kim (Konkuk University)
  • Hans Othmer (Dr. and Mrs.)

Description

Cancer is a complex, multi-scale process, in which genetic mutations occurring at a sub-cellular level manifest themselves as functional changes at the cellular and tissue scale. The main aim of this session is to discuss current stages and challenges in modelling tumour growth and developing therapeutic strategies. Specific goals of the session include: (i) to analyse both computational and analytical solutions to mathematical models from tumour modelling (ii) to discuss creative ways of laboratory experimentation for better clinical diagnosis (iii) to improve our biochemical/biomechanical understanding of fundamental mechanism of tumour growth such as analysis of signalling pathways in relative balances between oncogenes and suppressors. Both the immediate microenvironment (cell-cell or cell-matrix interactions) and the extended microenvironment (e.g. vascular bed, stromal cells) are considered to play major roles in tumour progression as well as suppression. Microenvironment is known to control tumour growth and cancer cell invasion to surrounding stromal tissue. However, it also prohibits therapeutics from accessing the tumour cells, thus causing drug resistance. Therefore, a thorough understanding of the microenvironment would provide a foundation to generate new strategies in therapeutic drug development. At the cellular level, cancer cell migration is a main step for metastasis and further progression of cancer and metastasis in a given microenvironment. Thus, understanding of cell motility under the control of signal transduction pathways in the presence of fibril network of ECM would improve technical and specific advances in cancer therapy by targeting the specific pathways that are associated with the diseases. Analysis of mathematical models would identify fundamental (abstract) structure of the model system and shed a light on our understanding of tumour growth in the specific host tissue environment and biochemical and biomechanical interactions between players in cancer progression. More comprehensive multi-scale (hybrid) models can be used to meet the needs of designing patient-specific agents.

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