Measuring kinetics and metastatic propensity of CTCs by blood exchange between mice

• Main Authors: Hamza, Bashar (Author), Miller, Alex B. (Author), Meier, Lara (Author), Stockslager, Max (Author), Ng, Sheng Rong (Author), King, Emily M. (Author), Lin, Lin (Author), DeGouveia, Kelsey L. (Author), Mulugeta, Nolawit (Author), Calistri, Nicholas L. (Author), Strouf, Haley (Author), Bray, Christina (Author), Rodriguez, Felicia (Author), Freed-Pastor, William A. (Author), Chin, Christopher R. (Author), Jaramillo, Grissel C. (Author), Burger, Megan L. (Author), Weinberg, Robert A. (Author), Shalek, Alex K. (Author), Jacks, Tyler (Author), Manalis, Scott R. (Author)
• Format: Article
• Language: English
• Published: Springer Science and Business Media LLC, 2022-05-23T14:42:27Z.
• Subjects: Article
• Online Access: Get fulltext

 <jats:title>Abstract</jats:title><jats:p>Existing preclinical methods for acquiring dissemination kinetics of rare circulating tumor cells (CTCs) en route to forming metastases have not been capable of providing a direct measure of CTC intravasation rate and subsequent half-life in the circulation. Here, we demonstrate an approach for measuring endogenous CTC kinetics by continuously exchanging CTC-containing blood over several hours between un-anesthetized, tumor-bearing mice and healthy, tumor-free counterparts. By tracking CTC transfer rates, we extrapolated half-life times in the circulation of between 40 and 260 s and intravasation rates between 60 and 107,000 CTCs/hour in mouse models of small-cell lung cancer (SCLC), pancreatic ductal adenocarcinoma (PDAC), and non-small cell lung cancer (NSCLC). Additionally, direct transfer of only 1−2% of daily-shed CTCs using our blood-exchange technique from late-stage, SCLC-bearing mice generated macrometastases in healthy recipient mice. We envision that our technique will help further elucidate the role of CTCs and the rate-limiting steps in metastasis.</jats:p>