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The extracellular matrix modulates the hallmarks of cancer

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TLDR
It is suggested that the success of cancer prevention and therapy programs requires an intimate understanding of the reciprocal feedback between the evolving extracellular matrix, the tumor cells and its cancer‐associated cellular stroma.
Abstract
The extracellular matrix regulates tissue development and homeostasis, and its dysregulation contributes to neoplastic progression. The extracellular matrix serves not only as the scaffold upon which tissues are organized but provides critical biochemical and biomechanical cues that direct cell growth, survival, migration and differentiation and modulate vascular development and immune function. Thus, while genetic modifications in tumor cells undoubtedly initiate and drive malignancy, cancer progresses within a dynamically evolving extracellular matrix that modulates virtually every behavioral facet of the tumor cells and cancer-associated stromal cells. Hanahan and Weinberg defined the hallmarks of cancer to encompass key biological capabilities that are acquired and essential for the development, growth and dissemination of all human cancers. These capabilities include sustained proliferation, evasion of growth suppression, death resistance, replicative immortality, induced angiogenesis, initiation of invasion, dysregulation of cellular energetics, avoidance of immune destruction and chronic inflammation. Here, we argue that biophysical and biochemical cues from the tumor-associated extracellular matrix influence each of these cancer hallmarks and are therefore critical for malignancy. We suggest that the success of cancer prevention and therapy programs requires an intimate understanding of the reciprocal feedback between the evolving extracellular matrix, the tumor cells and its cancer-associated cellular stroma.

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The extracellular matrix: Tools and insights for the "omics" era.

TL;DR: In this article, the extracellular matrix (ECM) is a fundamental component of multicellular organisms that provides mechanical and chemical cues that orchestrate cellular and tissue organization and functions.
References
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Journal ArticleDOI

Discoidin Domain Receptor 1 on Bone Marrow–Derived Cells Promotes Macrophage Accumulation During Atherogenesis

TL;DR: In vitro studies to investigate the mechanisms involved revealed that macrophages from Ddr1−/− mice had decreased adhesion to type IV collagen and decreased chemotactic invasion of typeIV collagen in response to monocyte chemoattractant protein-1.
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Host epithelial geometry regulates breast cancer cell invasiveness

TL;DR: This work suggests that the mechanical tone of nontumorigenic host epithelium directs the phenotype of tumor cells and provides additional insight into the instructive role of the mechanical tumor microenvironment.
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Current Status of Anti–Human Epidermal Growth Factor Receptor 2 Therapies: Predicting and Overcoming Herceptin Resistance

TL;DR: The basal molecular subtype as a predictor of increased risk in HER2+ breast cancer and a possible alternative cause of drug resistance are introduced.
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Type IV collagen modulates angiogenesis and neovessel survival in the rat aorta model

TL;DR: The observation that type IV collagen has dose-dependent effects on vascular elongation, proliferation, and stabilization, supports the concept that the developing basement membrane of neovessles acts as a solid-phase regulator of angiogenesis, whose function varies depending on the concentration of its molecular components.
Journal ArticleDOI

Extracellular matrix regulation of metabolism and implications for tumorigenesis.

TL;DR: An overview of death processes that contribute to the death of matrix-detached normal cells is provided and mechanisms that confer anchorage independence are described, with a focus on ECM regulation of cell metabolism.
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