Cancer cells traveling to distant tissues during metastasis must survive passing through the circulation. However, the influence of this fluid microenvironment on these cells is poorly understood. It was previously viewed that exposure to the hemodynamic shear forces within circulation was inhospitable to cancer cells, causing the cells to be destroyed. Recent evidence indicates that transformed cells are markedly more resistant to fluid shear stress when compared to non-transformed epithelial cells. Furthermore, these cells selectively adapt following exposure to fluid shear stresses and become more resistant to subsequent exposures to shear stress. The mechanisms behind this difference in phenotype and induced resistance are investigated. The elastic modulus, a measure of stiffness, may play a role in resistance and is shown to be altered upon exposure to fluid shear forces. Additionally, plasma membrane repair is a critical process in the resistance phenotype as cells sustain damage but are able to maintain viability. Cytoskeletal dynamics are also shown to play a role in resistance to fluid shear forces.
Mechanisms of resistance to fluid shear stress in malignant cells
Abstract
Details
- Title: Subtitle
- Mechanisms of resistance to fluid shear stress in malignant cells
- Creators
- Benjamin Lee Krog - University of Iowa
- Contributors
- Michael D. Henry (Advisor)Sarah Celeste Vigmostad (Advisor)James A. Ankrum (Committee Member)
- Resource Type
- Thesis
- Degree Awarded
- Master of Science (MS), University of Iowa
- Degree in
- Biomedical Engineering
- Date degree season
- Spring 2016
- DOI
- 10.17077/etd.d741ter4
- Publisher
- University of Iowa
- Number of pages
- x, 114 pages
- Copyright
- Copyright © 2016 Benjamin Lee Krog
- Language
- English
- Date submitted
- 09/05/2018
- Description illustrations
- illustrations (some color)
- Description bibliographic
- Includes bibliographical references (pages 109-114).
- Public Abstract (ETD)
During metastasis, cancer cells traverse the circulation to travel to a distant part of the body and set up a secondary, metastatic tumor site, often with lethal consequences. Yet, cancer cell behavior within this microcirculatory environment is poorly understood. It was previously believed that this intermediate step was inefficient and metastatic cells were sensitive to fluid shear forces. However, our group found that these malignant cancer cells are significantly more resistant to fluid shear stresses compared to normal, non-transformed cells. Additionally, these cells displayed an induced resistance to these stresses. Upon repeated exposure to brief pulses of high levels of fluid shear, cells became more resistant in subsequent exposures. The mechanisms behind this cell biology are investigated. Plasma membrane repair is a critical process in the resistance phenotype as cells sustain damage but are able to maintain viability. Cell structural dynamics and mechanical properties, such as stiffness, are shown to be influenced by exposure to fluid shear stresses.
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering
- Record Identifier
- 9983777141402771