Skip to main content
. 2017 Aug 22;7(14):3595–3607. doi: 10.7150/thno.18974

Figure 6.

Figure 6

Schematic illustration of Gint4.T effect on recruitment and activity of BM-MSCs into triple negative breast cancer microenvironment. Gint4.T targeting PDGFRβ inhibits BM-MSCs homing to cancer cells and their trans-differentiation into cancer associated fibroblasts (CAFs) as well as BM-MSC pro-metastatic function.