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Related Concept Videos

Metastasis02:30

Metastasis

Metastasis is the spread of cancer cells from the original site to distant locations in the body. Cancer cells can spread via blood vessels (hematogenous) as well as lymph vessels in the body.
Epithelial-to-Mesenchymal Transition
The epithelial-to-mesenchymal transition or EMT is a developmental process commonly observed in wound healing, embryogenesis, and cancer metastasis. EMT is induced by transforming growth factor-beta (TGF-β) or receptor tyrosine kinase (RTK) ligands, which further...
Cell Migration01:19

Cell Migration

Cell migration is a process by which the cells move from one location to another, playing an essential role in embryological development, repair and regeneration, immune response, and metastasis. Cells migrate in response to chemical or mechanical signals generated by specific organs or tissues. The overall mechanism includes three steps - polarization, protrusion, and release. Polarization involves the formation of a distinct cell front and rear, which determines the direction of movement.
Cell Migration01:09

Cell Migration

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Cell-matrix's Response to Mechanical Forces01:13

Cell-matrix's Response to Mechanical Forces

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Adaptive Mechanisms in Cancer Cells02:53

Adaptive Mechanisms in Cancer Cells

Cancer cells accumulate genetic changes at an abnormally rapid rate due to the defects in the DNA repair mechanisms. From an evolutionary perspective, such genetic instability is advantageous for cancer development. Mutant cell lines accumulate a series of beneficial mutations that contribute to their progression into cancer.
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Chemotaxis and Direction of Cell Migration01:21

Chemotaxis and Direction of Cell Migration

Cells can detect chemical cues in their environment and reorganize the cytoskeleton to migrate toward them or away from them. This directional migration, called chemotaxis, is essential during embryogenesis and development, immune response, tissue repair and regeneration, and reproduction. These chemical cues can either attract or repel the cell's movement. For example, axon development is determined by a combination of chemoattractants and chemorepellents that direct the growing axon towards...

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Related Experiment Video

Updated: May 24, 2026

Isolation of Primary Human Colon Tumor Cells from Surgical Tissues and Culturing Them Directly on Soft Elastic Substrates for Traction Cytometry
09:28

Isolation of Primary Human Colon Tumor Cells from Surgical Tissues and Culturing Them Directly on Soft Elastic Substrates for Traction Cytometry

Published on: June 4, 2015

Cellular traction stresses increase with increasing metastatic potential.

Casey M Kraning-Rush1, Joseph P Califano, Cynthia A Reinhart-King

  • 1Department of Biomedical Engineering, Cornell University, Ithaca, New York, United States of America.

Plos One
|March 6, 2012
PubMed
Summary

Metastatic cancer cells generate significantly higher forces than non-metastatic cells, suggesting cellular force generation is crucial for cancer metastasis. This finding aids understanding of physical mechanisms in tumor progression.

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High Throughput Traction Force Microscopy Using PDMS Reveals Dose-Dependent Effects of Transforming Growth Factor-β on the Epithelial-to-Mesenchymal Transition
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Polyacrylamide Gels for Invadopodia and Traction Force Assays on Cancer Cells
08:48

Polyacrylamide Gels for Invadopodia and Traction Force Assays on Cancer Cells

Published on: January 4, 2015

Area of Science:

  • Biophysics
  • Cancer Biology
  • Cell Mechanics

Background:

  • Cancer metastasis involves cells migrating through a complex microenvironment.
  • Physical mechanisms of cancer cell migration are poorly understood.
  • No clinical tests diagnose metastasis likelihood, despite its link to poor prognosis.

Purpose of the Study:

  • Investigate differences in cellular force generation between metastatic and non-metastatic cancer cells.
  • Understand the physical mechanisms of cancer cell migration.
  • Explore the role of the extracellular microenvironment in metastasis.

Main Methods:

  • Traction force microscopy was used to measure cellular forces.
  • Human metastatic and non-metastatic cancer cell lines (breast, prostate, lung) were studied.
  • Experiments were conducted across varying matrix stiffness and collagen densities.

Main Results:

  • Metastatic cancer cells exhibited significantly increased traction stresses compared to non-metastatic cells.
  • Increased matrix stiffness and collagen density correlated with higher traction forces.
  • Cell spreading showed a direct relationship with collagen density and a biphasic relationship with stiffness.

Conclusions:

  • Cellular contractile force plays a critical role in cancer metastasis.
  • The physical properties of the tumor microenvironment regulate cancer cell force generation.
  • Findings are vital for understanding metastasis physical mechanisms and microenvironmental influences.