4.3 Review

The role of the microenvironment in tumor growth and invasion

期刊

PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY
卷 106, 期 2, 页码 353-379

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pbiomolbio.2011.06.006

关键词

Tumor progression; Mechanical effects; Hybrid model; Breast cancer

资金

  1. NIH [29123]
  2. NSF [0517884, 0817529]
  3. Minnesota Supercomputing Institute
  4. University of Michigan-Ann Arbor
  5. Direct For Mathematical & Physical Scien
  6. Division Of Mathematical Sciences [0517884, 0817529] Funding Source: National Science Foundation

向作者/读者索取更多资源

Mathematical modeling and computational analysis are essential for understanding the dynamics of the complex gene networks that control normal development and homeostasis, and can help to understand how circumvention of that control leads to abnormal outcomes such as cancer. Our objectives here are to discuss the different mechanisms by which the local biochemical and mechanical microenvironment, which is comprised of various signaling molecules, cell types and the extracellular matrix (ECM), affects the progression of potentially-cancerous cells, and to present new results on two aspects of these effects. We first deal with the major processes involved in the progression from a normal cell to a cancerous cell at a level accessible to a general scientific readership, and we then outline a number of mathematical and computational issues that arise in cancer modeling. In Section 2 we present results from a model that deals with the effects of the mechanical properties of the environment on tumor growth, and in Section 3 we report results from a model of the signaling pathways and the tumor microenvironment (TME), and how their interactions affect the development of breast cancer. The results emphasize anew the complexities of the interactions within the TME and their effect on tumor growth, and show that tumor progression is not solely determined by the presence of a clone of mutated immortal cells, but rather that it can be 'community-controlled'. (C) 2011 Elsevier Ltd. All rights reserved.

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