转移
乳腺癌
肿瘤坏死因子α
坏死
病理
癌症研究
医学
血管生成素
癌症
血管内皮生长因子
免疫学
内科学
血管内皮生长因子受体
作者
Ami Yamamoto,Yin Huang,Brad A. Krajina,Margaux McBirney,Andrea E. Doak,Sixuan Qu,Carolyn L. Wang,Michael Häffner,Kevin J. Cheung
标识
DOI:10.1073/pnas.2214888120
摘要
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.
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