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Review
. 2015;20(3-4):301-14.
doi: 10.1615/critrevoncog.2015013668.

Physiological, Tumor, and Metastatic Niches: Opportunities and Challenges for Targeting the Tumor Microenvironment

Affiliations
Review

Physiological, Tumor, and Metastatic Niches: Opportunities and Challenges for Targeting the Tumor Microenvironment

Meera Murgai et al. Crit Rev Oncog. 2015.

Abstract

The primary tumor niche and the related but distinct premetastatic/metastatic niche comprise a number of essential players, including immune cells, stromal cells, and extracellular matrix. The cross-talk between these components is key to tumor progression. Many of these cell types and signaling pathways in the tumor microenvironment also are found in physiological and stem cell niches, such as the bone marrow, colonic crypt, and skin bulge. Here they play tightly regulated roles in wound healing and tissue homeostasis. Understanding the similarities and differences between these distinct niches may better inform our ability to therapeutically target the tumor microenvironment. In this review we discuss a number of tumor and metastatic niche components as they relate to stem cell niches and highlight potential therapeutic strategies in pediatric cancers.

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Figures

FIG. 1
FIG. 1
Commonalities of pathological and physiological niche environments. The primary tumor niche and the related but distinct premetastatic/metastatic niche comprise a number of key players that promote tumor progression. Many of these molecular and cellular components also are found in physiological niches such as the bone marrow, colonic crypt, and skin bulge, where they play tightly regulated roles in wound healing and tissue homeostasis. Soluble factors such as growth factors and interleukins that play a key role in these stem cell niches also are produced by the tumor and can influence cells of the primary tumor niche and premetastatic/metastatic niche to promote tumor cell proliferation, migration, and spread. Understanding the similarities and differences between these distinct niches may better inform the ability to therapeutically target the tumor microenvironment.

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