Collagen-rich airway smooth muscle cells are a metastatic niche for tumor colonization in the lung.

ABSTRACT: Metastases account for the majority of cancer deaths. While certain steps of the metastatic cascade are well characterized, identification of targets to block this process remains a challenge. Host factors determining metastatic colonization to secondary organs are particularly important for exploration, as those might be shared among different cancer types. Here, we showed that bladder tumor cells expressing the collagen receptor, CD167a, responded to collagen I stimulation at the primary tumor to promote local invasion and utilized the same receptor to preferentially colonize at airway smooth muscle cells (ASMCs)-a rich source of collagen III in lung. Morphologically, COL3-CD167a-driven metastatic foci are uniquely distinct from typical lung alveolar metastatic lesions and exhibited acti

SUBMITTER: Lee YC 

PROVIDER: S-EPMC6513865 | biostudies-literature | 2019 May

REPOSITORIES: biostudies-literature