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DESCRIPTION (provided by applicant): The goal of this cross-disciplinary project is to produce mathematical models and simulation software that describe quantitatively the process of cancer invasion and encapsulate the knowledge derived from a wide range of experimental observations into a correlative and predictive tool, available to all researchers. Cancer invasion is thought to involve a number of cellular parameters (including altered rates of cell proliferation, apoptosis, migration, adhesion, metabolism, and mutation), as well as microenvironmental parameters (including extracellular matrix composition, angiogenesis, inflammation, and proteases). From a mathematical point of view, some of these parameters are continuous and some discrete. Therefore, our primary approach is based on a hybrid model in which both continuum deterministic and discrete stochastic parameters and variables are integrated. Because of its hybrid nature, the model can be directly linked to experimental measurements of those cellular and microenvironmental parameters recognized by cancer biologists as important in cancer invasion. Predictions based on the hybrid models will be visualized by software that implements computer simulations of invasion. These models and the associated simulations will be the basis for generating hypotheses that will be tested in vitro, in two-dimensional (2D) and three-dimensional (3D) cancer cell culture systems, as well as in vivo, in xenograft and genetic mouse models for human cancers. Experimental validation will be used to both refine and improve the mathematical models and simulation programs in an iterative fashion and provide new input parameters for the models. Initially, we will model invasion parameters at a level of complexity that does not hinder mathematical and experimental feasibility, but that already provides a realistic representation of cancer invasion. As we progress, we will be able to introduce increasing levels of complexity, since the model is open to incorporation of parameters and experimental data from several scales, e.g., the macro-scale (tissue), micro-scale (cells), subcellular, and molecular scales. The long-term goal is to produce a comprehensive, quantitative description of the major mechanisms underlying cancer invasion. This description, and the associated computer simulations, should enable a rational approach for accurate diagnostic staging and therapeutic targeting of the invasion/metastasis step of cancer progression.
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Phenotype Heterogeneity and Dynamics in SCLC
  • 批准号:
    9901484
  • 项目类别:
  • 资助金额:
    $173.3万
  • 财政年份:
    2018
  • 负责人:
    Vito Quaranta
  • 依托单位:
Administrative Core
  • 批准号:
    10375419
  • 项目类别:
  • 资助金额:
    $19.96万
  • 财政年份:
    2018
  • 负责人:
    Vito Quaranta
  • 依托单位:
Phenotype Heterogeneity and Dynamics in SCLC
  • 批准号:
    10375418
  • 项目类别:
  • 资助金额:
    $154.69万
  • 财政年份:
    2018
  • 负责人:
    Vito Quaranta
  • 依托单位:
Modeling the SCLC Phenotypic Space
  • 批准号:
    10375422
  • 项目类别:
  • 资助金额:
    $51.56万
  • 财政年份:
    2018
  • 负责人:
    Vito Quaranta
  • 依托单位:
国内基金
海外基金
Epac1/2通过蛋白酶体调控中性粒细胞NETosis和Apoptosis在急性肺损伤中的作用研究
  • 批准号:
    LBY21H010001
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2020
  • 负责人:
    郑绪阳
  • 依托单位:
基于Apoptosis/Ferroptosis双重激活效应的天然产物AlbiziabiosideA的抗肿瘤作用机制研究及其结构改造
  • 批准号:
    81703335
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    20.0万元
  • 批准年份:
    2017
  • 负责人:
    卫高菲
  • 依托单位:
双肝移植后Apoptosis和pyroptosis在移植物萎缩差异中的作用和供受者免疫微环境变化研究
  • 批准号:
    81670594
  • 项目类别:
    面上项目
  • 资助金额:
    58.0万元
  • 批准年份:
    2016
  • 负责人:
    陈昊
  • 依托单位:
Serp-2 调控apoptosis和pyroptosis 对肝脏缺血再灌注损伤的保护作用研究
  • 批准号:
    81470791
  • 项目类别:
    面上项目
  • 资助金额:
    73.0万元
  • 批准年份:
    2014
  • 负责人:
    董家鸿
  • 依托单位: