Abstract

Although the mechanisms underlying the genesis and progression of breast cancer are better understood than ever, it is still the most frequent malignant tumor in women and one of the leading causes of cancer death. Therefore, we need to establish new approaches that lead us to better understand the prognosis of this heterogeneous systemic disease and to propose new therapeutic strategies. Cancer is not only a malignant transformation of the epithelial cells merely based on their autonomous or acquired proliferative capacity. Today, data support the concept of cancer as an ecosystem based on a cellular sociology, with diverse components and complex interactions between them. Among the different cell types that make up the stroma, which have a relevant role in the dynamics of tumor/stromal cell interactions, the main ones are cancer associated fibroblasts, endothelial cells, immune cells and mesenchymal stromal cells. Several factors expressed by the stroma of breast carcinomas are associated with the development of metastasis, such as matrix metalloproteases, their tissular inhibitors or some of their regulators like integrins, cytokines or toll-like receptors. Based on the expression of these factors, two types of breast cancer stroma can be proposed with significantly different influence on the prognosis of patients. In addition, there is evidence about the existence of bi-directional signals between cancer cells and tumor stroma cells with prognostic implications, suggesting new therapeutic strategies in breast cancer.

Highlights

  • Breast cancer is the most frequent malignant tumor in women and the leading cause of cancer death, since 30% of breast cancers develop distant metastases after the initial treatment of the apparently localized tumors [1]

  • Considering that the expression of Metastasis metalloproteases (MMPs)-11 may constitute a useful biological marker for pro-metastatic mononuclear inflammatory cells (MICs), we investigated its relationship with the gene expression of 65 factors associated with inflammation and tumor progression in a population of breast cancer patients stratified into two groups according to MMP-11 expression by intratumoral

  • We have shown that TLR4 expression by MICs was associated with an increased incidence of metastasis, whereas TLR9 expression by cancer-associated fibroblasts (CAFs) was associated with a low metastasis-rate [115], pointing towards a protective role of TLR9 against tumor progression

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Summary

Introduction

Breast cancer is the most frequent malignant tumor in women and the leading cause of cancer death, since 30% of breast cancers develop distant metastases after the initial treatment of the apparently localized tumors [1]. The mechanisms underlying the genesis and progression of breast cancer are better understood [2], but despite an improvement of the survival rates for some molecular subtypes of breast cancer, we are still far from a cure for all patients [3]. A better knowledge of the role of tumor stroma and its interaction with cancer cells can lead us to implement new prognostic tools or new therapeutic strategies aiming at a disruption of the dynamics of tumor-stroma interactions. We reviewed several key pathophysiological aspects related to tumor stroma and breast cancer progression, their clinical implications and possible therapeutic opportunities

Tumor Stroma Components
Immune Cells
Endothelial Cells
Mesenchymal Stromal Cells
Phenotype
Cytokines
Integrins
Intercellular Communication System in the Tumor Microenvironment
Soluble Factors
Exosomes
Integrins and Cancer
Tumor Stroma and Therapeutic Opportunities
Findings
Conclusions and Future Perspectives
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