Cellular interactions in the vascular niche: Implications in the regulation of tumor dormancy

Research output: Contribution to journalArticle

39 Citations (Scopus)

Abstract

Angiogenesis plays an established role in the promotion of growth of dormant micrometastasis, because blood vessels deliver oxygen and nutrients to the tumor microenvironment. In addition to this feeding function, however, there is accumulating evidence suggesting that endothelial cells - and perhaps other cellular components of the microenvironment - could communicate both positive and negative signals to tumor cells. This cross-talk between heterogeneous cell types could turn out to be important in the regulation of cancer cell behavior. Normal cells recruited during the angiogenic process, or attracted to future sites of metastasis by soluble products released by cancer cells, have been shown to create a niche favorable to tumor cell proliferation and survival. In addition, following an exogenous angiogenic spike, as may occur during inflammation, the same mechanisms could lead to re-activation of poorly angiogenic tumor cells seeded into tissues. In this review, we discuss the possible implications of this hypothesis for our understanding of the phenomenon of tumor dormancy.

Original languageEnglish
Pages (from-to)648-659
Number of pages12
JournalAPMIS
Volume116
Issue number7-8
DOIs
Publication statusPublished - Jul 2008

Fingerprint

Blood Vessels
Neoplasms
Cellular Microenvironment
Neoplasm Micrometastasis
Tumor Microenvironment
Cell Survival
Endothelial Cells
Cell Proliferation
Oxygen
Neoplasm Metastasis
Inflammation
Food
Growth

Keywords

  • Angiogenesis
  • Cancer stem cell
  • Notch
  • Tumor dormancy
  • VEGF

ASJC Scopus subject areas

  • Immunology
  • Microbiology (medical)
  • Pathology and Forensic Medicine

Cite this

Cellular interactions in the vascular niche : Implications in the regulation of tumor dormancy. / Favaro, Elena; Amadori, Alberto; Indraccolo, Stefano.

In: APMIS, Vol. 116, No. 7-8, 07.2008, p. 648-659.

Research output: Contribution to journalArticle

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