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A Simple Migration/Invasion Workflow Using an Automated Live-cell Imager
Published on: February 2, 2019
Physiological mechanisms of tumor-cell invasion and migration
David H Geho1, Russell W Bandle, Timothy Clair
1Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA. gehod@mail.nih.gov
Abstract:
Recent advances in understanding the complex biology of the microenvironment that underlies tumor invasion and migration have revealed novel and promising therapeutic targets. Pharmacological blockade of intra- and extracellular signaling events that regulate migration and survival of multiple cell types may disrupt the host-tumor conspiracy that allows escape from normal developmental regulation.
Insights
Understanding tumor microenvironment biology reveals new therapeutic targets for blocking cancer cell invasion and migration. Targeting signaling pathways may disrupt tumor escape mechanisms, offering novel treatment strategies.
Area of Science:
- Oncology
- Cancer Biology
- Molecular Biology
Background:
- The tumor microenvironment plays a critical role in cancer progression, specifically in tumor invasion and migration.
- Complex signaling networks within and outside tumor cells facilitate cancer cell escape from normal regulatory processes.
Purpose of the Study:
- To identify and explore novel therapeutic targets within the tumor microenvironment.
- To investigate the potential of blocking signaling events to inhibit tumor cell migration and survival.
Main Methods:
- Review of recent advances in tumor microenvironment research.
- Analysis of intra- and extracellular signaling pathways regulating cell migration and survival.
Main Results:
- Identification of novel therapeutic targets based on understanding tumor microenvironment biology.
- Potential for pharmacological blockade of signaling events to disrupt tumor invasion and migration.
Conclusions:
- Targeting specific signaling pathways in the tumor microenvironment offers a promising therapeutic strategy.
- Disrupting the host-tumor interactions that promote cancer cell escape may lead to more effective cancer treatments.
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