Cancer Invasion: Patterns and Mechanisms

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Abstract

Cancer invasion and the ability of malignant tumor cells for directed migration and metastasis have remained a focus of research for many years. Numerous studies have confirmed the existence of two main patterns of cancer cell invasion: collective cell migration and individual cell migration, by which tumor cells overcome barriers of the extracellular matrix and spread into surrounding tissues. Each pattern of cell migration displays specific morphological features and the biochemical/molecular genetic mechanisms underlying cell migration. Two types of migrating tumor cells, mesenchymal (fibroblast-like) and amoeboid, are observed in each pattern of cancer cell invasion. This review describes the key differences between the variants of cancer cell migration, the role of epithelial-mesenchymal, collective-amoeboid, mesenchymal-amoeboid, and amoeboid-mesenchymal transitions, as well as the significance of different tumor factors and stromal molecules in tumor invasion. The data and facts collected are essential to the understanding of how the patterns of cancer cell invasion are related to cancer progression and therapy efficacy. Convincing evidence is provided that morphological manifestations of the invasion patterns are characterized by a variety of tissue (tumor) structures. The results of our own studies are presented to show the association of breast cancer progression with intratumoral morphological heterogeneity, which most likely reflects the types of cancer cell migration and results from different activities of cell adhesion molecules in tumor cells of distinct morphological structures.

About the authors

N. V. Krakhmal

Siberian State Medical University

Email: d_evgeniy@oncology.tomsk.ru
Russian Federation

M. V. Zavyalova

Siberian State Medical University; Tomsk Cancer Research Institute; Tomsk State University

Email: d_evgeniy@oncology.tomsk.ru
Russian Federation

E. V. Denisov

Tomsk Cancer Research Institute; Tomsk State University

Author for correspondence.
Email: d_evgeniy@oncology.tomsk.ru
Russian Federation

S. V. Vtorushin

Siberian State Medical University; Tomsk Cancer Research Institute

Email: d_evgeniy@oncology.tomsk.ru
Russian Federation

V. M. Perelmuter

Siberian State Medical University; Tomsk Cancer Research Institute

Email: d_evgeniy@oncology.tomsk.ru
Russian Federation

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