Publication | Open Access
Tumor cell α3β1 integrin and vascular laminin-5 mediate pulmonary arrest and metastasis
195
Citations
49
References
2004
Year
Tumor BiologyAlpha3beta1 IntegrinImmunologyCancer GrowthSize RestrictionBronchial NeoplasmCell-matrix InteractionVascular BiologyCellular PhysiologyIntegrin ContactsMatrix BiologyRadiation OncologyMedicineCell BiologyTumor MicroenvironmentLung CancerCancer ResearchPulmonary Vascular Disease
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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