Tumor cell α3β1 integrin and vascular laminin-5 mediate pulmonary arrest and metastasis

Hui Wang(Children's Hospital of Philadelphia), Weili Fu(Children's Hospital of Philadelphia), Jae Hong Im(Children's Hospital of Philadelphia), Zengyi Zhou(Children's Hospital of Philadelphia), Samuel A. Santoro(Vanderbilt University), Vandana Iyer(Albany Medical Center Hospital), C. Mike DiPersio(Albany Medical Center Hospital), Qian‐Chun Yu(University of Pennsylvania), Vito Quaranta(Vanderbilt University), Abu B. Al‐Mehdi(University of South Alabama), Ruth J. Muschel(Children's Hospital of Philadelphia)
The Journal of Cell Biology
March 15, 2004
Cited by 195Open Access
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Abstract

Arrest of circulating tumor cells in distant organs is required for hematogenous metastasis, but the tumor cell surface molecules responsible have not been identified. Here, we show that the tumor cell alpha3beta1 integrin makes an important contribution to arrest in the lung and to early colony formation. These analyses indicated that pulmonary arrest does not occur merely due to size restriction, and raised the question of how the tumor cell alpha3beta1 integrin contacts its best-defined ligand, laminin (LN)-5, a basement membrane (BM) component. Further analyses revealed that LN-5 is available to the tumor cell in preexisting patches of exposed BM in the pulmonary vasculature. The early arrest of tumor cells in the pulmonary vasculature through interaction of alpha3beta1 integrin with LN-5 in exposed BM provides both a molecular and a structural basis for cell arrest during pulmonary metastasis.


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