Related Experiment Video
Updated: Dec 7, 2025

Analysis of Cell Migration within a Three-dimensional Collagen Matrix
Published on: October 5, 2014
Cell Adhesion Molecules in Plasticity and Metastasis
Jessica A Smart1, Julia E Oleksak2, Edward J Hartsough3
1Department of Pharmacology and Physiology, Drexel University College of Medicine, Philadelphia, Pennsylvania.
Abstract:
Prior to metastasis, modern therapeutics and surgical intervention can provide a favorable long-term survival for patients diagnosed with many types of cancers. However, prognosis is poor for patients with metastasized disease. Melanoma is the deadliest form of skin cancer, yet in situ and localized, thin melanomas can be biopsied with little to no postsurgical follow-up. However, patients with metastatic melanoma require significant clinical involvement and have a 5-year survival of only 34% to 52%, largely dependent on the site of colonization. Melanoma metastasis is a multi-step process requiring dynamic changes in cell surface proteins regulating adhesiveness to the extracellular matrix (ECM), stroma, and other cancer cells in varied tumor microenvironments. Here we will highlight recent literature to underscore how cell adhesion molecules (CAM) contribute to melanoma disease progression and metastasis.
Related Concept Videos
Cell Adhesion Molecules - Types and Functions
CAM Families
The Integrin family of proteins is primarily involved...
Overview of Cell-Matrix Interactions
Metastasis
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...
Intracellular Signaling Affects Focal Adhesions
Some...
Selectins
Cell Migration

