| Literature DB >> 29417941 |
Rong-Rui Wei1, Dan-Ni Sun2, Hong Yang2, Juan Yan2, Xiong Zhang2, Xing-Ling Zheng2, Xu-Hong Fu2, Mei-Yu Geng2, Xun Huang3, Jian Ding4.
Abstract
Aggregated metastatic cancer cells, referred to as circulating tumor cell (CTC) clusters, are present in the blood of cancer patients and contribute to cancer metastasis. However, the origin of CTC clusters, especially intravascular aggregates, remains unknown. Here, we employ suspension culture methods to mimic CTC cluster formation in the circulation of breast cancer patients. CTC clusters generated using these methods exhibited an increased metastatic potential that was defined by the overexpression of heparanase (HPSE). Heparanase induced FAK- and ICAM-1-dependent cell adhesion, which promoted intravascular cell aggregation. Moreover, knockdown of heparanase or inhibition of its activity with JG6, a heparanase inhibitor, was sufficient to block the formation of cell clusters and suppress breast cancer metastasis. Our data reveal that heparanase-mediated cell adhesion is critical for metastasis mediated by intravascular CTC clusters. We also suggest that targeting the function of heparanase in cancer cell dissemination might limit metastatic progression.Entities:
Keywords: CTC clusters; adhesion molecules; cell adhesion; heparanase; human breast cancer; metastasis; suspension culture method
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Year: 2018 PMID: 29417941 PMCID: PMC6289387 DOI: 10.1038/aps.2017.189
Source DB: PubMed Journal: Acta Pharmacol Sin ISSN: 1671-4083 Impact factor: 6.150