4.8 Article

Imaging Tumor-Stroma Interactions during Chemotherapy Reveals Contributions of the Microenvironment to Resistance

期刊

CANCER CELL
卷 21, 期 4, 页码 488-503

出版社

CELL PRESS
DOI: 10.1016/j.ccr.2012.02.017

关键词

-

资金

  1. National Cancer Institute [U01 CA141451, R01 CA057621, P50 CA088843]
  2. Starr Cancer Consortium
  3. Breast Cancer Alliance
  4. Cancer-American Association for Cancer Research Dream Team Translational Cancer Research [SU2C-AACR-DT0409]
  5. Congressionally Directed Breast Cancer Research Program, U.S.
  6. Research Council of Norway [160698/V40, 151882]
  7. Southeastern Regional Health Authorities [2007060]
  8. William Randolph Hearst Foundation
  9. Watson School of Biological Sciences
  10. University of Oslo Research Fund (UNIFOR)
  11. Ulleval University Hospital Research Fund (VIRUUS)

向作者/读者索取更多资源

Little 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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据