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Fig. 7 | Journal of Experimental & Clinical Cancer Research

Fig. 7

From: Tumor-derived exosomal ADAM17 promotes pre-metastatic niche formation by enhancing vascular permeability in colorectal cancer

Fig. 7

A schematic model showing the functions of exosomal ADAM17 in CRC hematogenous metastasis. The current study indicated the presence of intercellular communication between mesenchymal cancer cells and the vascular endothelium. EMT-CRC-derived exosomal ADAM17 disrupts expression of the adherent junction protein VE-cadherin, thus dysregulating the vascular barrier and facilitating the generation of CTCs and metastasis

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