Metastasis from the tumor interior and necrotic core formation are regulated by breast cancer-derived angiopoietin-like 7

Author:

Yamamoto Ami123,Huang Yin12,Krajina Brad A.12,McBirney Margaux12,Doak Andrea E.123,Qu Sixuan12,Wang Carolyn L.4,Haffner Michael C.256ORCID,Cheung Kevin J.12

Affiliation:

1. Translational Research Program, Public Health Sciences Division, Fred Hutchinson Cancer Center, Seattle, WA 98109

2. Human Biology Division, Fred Hutchinson Cancer Center, Seattle, WA 98109

3. Molecular and Cellular Biology Graduate Program, University of Washington, Seattle, WA 98195

4. Department of Radiology, University of Washington School of Medicine, Seattle, WA 98195

5. Division of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA 98109

6. Division of Clinical Research, Fred Hutchinson Cancer Center, Seattle, WA 98109

Abstract

Necrosis in the tumor interior is a common feature of aggressive cancers that is associated with poor clinical prognosis and the development of metastasis. How the necrotic core promotes metastasis remains unclear. Here, we report that emergence of necrosis inside the tumor is correlated temporally with increased tumor dissemination in a rat breast cancer model and in human breast cancer patients. By performing spatially focused transcriptional profiling, we identified angiopoietin-like 7 (Angptl7) as a tumor-specific factor localized to the perinecrotic zone. Functional studies showed that Angptl7 loss normalizes central necrosis, perinecrotic dilated vessels, metastasis, and reduces circulating tumor cell counts to nearly zero. Mechanistically, Angptl7 promotes vascular permeability and supports vascular remodeling in the perinecrotic zone. Taken together, these findings show that breast tumors actively produce factors controlling central necrosis formation and metastatic dissemination from the tumor core.

Funder

U.S. Department of Defense

Susan G. Komen

HHS | NIH | National Cancer Institute

Burroughs Wellcome

V Foundation for Cancer Research

Seattle Translational Tumor Research

Doris Duke Charitable Foundation

GE | GE Healthcare

HHS | NIH | National Institute of General Medical Sciences

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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