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Review
. 2016 Sep;142(9):1897-907.
doi: 10.1007/s00432-016-2145-0. Epub 2016 Mar 17.

The emerging roles of exosomes in tumor-stroma interaction

Affiliations
Review

The emerging roles of exosomes in tumor-stroma interaction

Hailong Fu et al. J Cancer Res Clin Oncol. 2016 Sep.

Abstract

Purpose: The tumor-stroma interaction is critical for the development and progression of cancer. Cancer-associated fibroblasts (CAFs), one of the major components of the tumor stroma, can promote tumor growth and metastasis. Exosomes are secreted microvesicles that mediate cell-to-cell communication. Exosomal contents, including proteins, nucleic acids, and lipids, can be shuttled from donor cells to target cells. Recent studies suggest that exosomes play important roles in the tumor-stroma interaction. Herein, we review the multifaceted roles of exosomes in the tumor-stroma interaction and the underlying molecular mechanisms.

Methods: Literature search for all relevant publications was performed on PubMed databases. The keywords of exosomes, tumor, stroma, CAFs, mesenchymal stem cells (MSCs) and other closely related terms were used for searching.

Results: Tumor cell-derived exosomes induce the differentiation of fibroblasts and MSCs into CAFs. In turn, exosomes secreted by CAFs promote tumor growth, metastasis, and drug resistance through distinct mechanisms. Moreover, exosomes from stromal cells can be used as therapeutic vehicles for the delivery of anticancer drugs.

Conclusions: Tumor cells communicate with CAFs through exosomes, which establishes a bidirectional cross talk to promote tumor growth, metastasis, and drug resistance. Targeting exosomes in tumor-stroma interaction may have important implications for anticancer therapy.

Keywords: Cancer-associated fibroblasts; Exosomes; Stroma; Tumor.

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Conflict of interest statement

The authors declare that they have no conflict of interest.

Figures

Fig. 1
Fig. 1
The roles of exosomes in tumor-CAFs interaction. The membrane of the multivesicular bodies (MVBs) bulges inward to form exosomes. During this process, nucleic acids, proteins, and lipids are packed into exosomes in a cell-type-dependent manner. MVBs fuse with the cellular membrane to release exosomes into the extracellular space. Recipient cells internalize exosomes through endocytosis by phagocytosis, receptor–ligand interaction, and fusion with the cell membrane. Exosomes are involved in tumor initiation, growth, metastasis, angiogenesis, and drug resistance by delivering oncogenic proteins and nucleic acids. Tumor cell-derived exosomes are involved in the formation of tumor stroma by inducing the differentiation of fibroblasts, mesenchymal stem cells, and other bone marrow-derived cells into CAFs. In turn, CAF-derived exosomes promote tumor growth, metastasis, and drug resistance through multiple mechanisms

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