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Open AccessJournal ArticleDOI

Remodeling of the mammary microenvironment after lactation promotes breast tumor cell metastasis.

TLDR
It is suggested that the mammary gland microenvironment becomes promotional for tumor cell dissemination during involution, thus providing a plausible mechanism to explain the high rate of metastases that occur with pregnancy-associated breast cancer.
Abstract
The mammary gland microenvironment during postlactational involution shares similarities with inflammation, including high matrix metalloproteinase activity, fibrillar collagen deposition, and release of bioactive fragments of fibronectin and laminin. Because inflammation can promote tumorigenesis, we evaluated whether the tissue microenvironment of the involuting gland is also promotional. Extracellular matrix was isolated from mammary glands of nulliparous rats or rats with mammary glands undergoing weaning-induced involution. Using these matrices as substratum, nulliparous matrix was found to promote ductal organization of normal mammary epithelial MCF-12A cells in three-dimensional culture and to suppress invasion of mammary tumor MDA-MB-231 cells in transwell filter assays. Conversely, involution matrix failed to support ductal development in normal cells and promoted invasiveness in tumor cells. To evaluate the effects of these matrices on metastasis in vivo, MDA-MB-231 cells, premixed with Matrigel, nulliparous matrix, or involution matrix, were injected into mammary fat pads of nude mice. Metastases to lung, liver, and kidney were increased in the involution matrix group, and correlated with a twofold increase in tumor vascular endothelial growth factor expression and increased angiogenesis. These data suggest that the mammary gland microenvironment becomes promotional for tumor cell dissemination during involution, thus providing a plausible mechanism to explain the high rate of metastases that occur with pregnancy-associated breast cancer.

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A Tense Situation: Forcing Tumour Progression

TL;DR: The changing force that cells experience needs to be considered when trying to understand the complex nature of tumorigenesis.
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Modeling Tissue Morphogenesis and Cancer in 3D

TL;DR: Three-dimensional (3D) in vitro models provide unique perspectives on the behavior of stem cells, developing tissues and organs, and tumors and may help to accelerate translational research in cancer biology and tissue engineering.
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Aligned collagen is a prognostic signature for survival in human breast carcinoma.

TL;DR: It is proposed that quantifying collagen alignment is a viable, novel paradigm for the prediction of human breast cancer survival because of the strong statistical evidence for poor survival in patients with TACS and because the assessment can be performed in routine histopathological samples imaged via second harmonic generation or using picrosirius.
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Breast cancer: origins and evolution

TL;DR: This work states that although tumor initiation and progression are predominantly driven by acquired genetic alterations, recent data implicate a role for microenvironmental and epigenetic changes as well.
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Mammary gland development

TL;DR: The knowledge of mammary gland development and mammary stem cell biology has significantly contributed to the understanding of breast cancer and has advanced the discovery of therapies to treat this disease.
References
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Journal ArticleDOI

Inflammation and cancer

TL;DR: It is now becoming clear that the tumour microenvironment, which is largely orchestrated by inflammatory cells, is an indispensable participant in the neoplastic process, fostering proliferation, survival and migration.
Book ChapterDOI

Cell death : the significance of apoptosis

TL;DR: It has proved feasible to categorize most if not all dying cells into one or the other of two discrete and distinctive patterns of morphological change, which have, generally, been found to occur under disparate but individually characteristic circumstances.
Journal ArticleDOI

A multigenic program mediating breast cancer metastasis to bone.

TL;DR: Overexpression of this bone metastasis gene set is superimposed on a poor-prognosis gene expression signature already present in the parental breast cancer population, suggesting that metastasis requires a set of functions beyond those underlying the emergence of the primary tumor.
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