Author/Authors :
Nakasone، نويسنده , , Elizabeth S. and Askautrud، نويسنده , , Hanne A. and Kees، نويسنده , , Tim and Park، نويسنده , , Jae-Hyun and Plaks، نويسنده , , Vicki and Ewald، نويسنده , , Andrew J. and Fein، نويسنده , , Miriam and Rasch، نويسنده , , Morten G. and Tan، نويسنده , , Ying-Xim and Qiu، نويسنده , , Jing and Park، نويسنده , , Juwon and Sinha، نويسنده , , Pranay and Bissell، نويسنده , , Mina J. and Frengen، نويسنده , , Eirik and Werb، نويسنده , , Zena and Egeblad، نويسنده , , Mikala، نويسنده ,
Abstract :
Summary
is known about the dynamics of cancer cell death in response to therapy in the tumor microenvironment. Intravital microscopy of chemotherapy-treated mouse mammary carcinomas allowed us to follow drug distribution, cell death, and tumor-stroma interactions. We observed associations between vascular leakage and response to doxorubicin, including improved response in matrix metalloproteinase-9 null mice that had increased vascular leakage. Furthermore, we observed CCR2-dependent infiltration of myeloid cells after treatment and that Ccr2 null host mice responded better to treatment with doxorubicin or cisplatin. These data show that the microenvironment contributes critically to drug response via regulation of vascular permeability and innate immune cell infiltration. Thus, live imaging can be used to gain insights into drug responses in situ.
