4.4 Article

Adaptation of Semiautomated Circulating Tumor Cell (CTC) Assays for Clinical and Preclinical Research Applications

期刊

出版社

JOURNAL OF VISUALIZED EXPERIMENTS
DOI: 10.3791/51248

关键词

Medicine; Issue 84; Metastasis; circulating tumor cells (CTCs); CellSearch system; user defined marker characterization; in vivo; preclinical mouse model; clinical research

资金

  1. Ontario Institute of Cancer Research [08NOV230]
  2. Canada Foundation for Innovation [13199]
  3. Prostate Cancer Canada
  4. London Regional Cancer Program
  5. Frederick Banting and Charles Best Canada Graduate Scholarship Doctoral Award
  6. CIHR New Investigator Award
  7. Ontario Ministry of Research and Innovation
  8. John and Donna Bristol through the London Health Sciences Foundation
  9. Janssen Oncology

向作者/读者索取更多资源

The majority of cancer-related deaths occur subsequent to the development of metastatic disease. This highly lethal disease stage is associated with the presence of circulating tumor cells (CTCs). These rare cells have been demonstrated to be of clinical significance in metastatic breast, prostate, and colorectal cancers. The current gold standard in clinical CTC detection and enumeration is the FDA-cleared CellSearch system (CSS). This manuscript outlines the standard protocol utilized by this platform as well as two additional adapted protocols that describe the detailed process of user-defined marker optimization for protein characterization of patient CTCs and a comparable protocol for CTC capture in very low volumes of blood, using standard CSS reagents, for studying in vivo preclinical mouse models of metastasis. In addition, differences in CTC quality between healthy donor blood spiked with cells from tissue culture versus patient blood samples are highlighted. Finally, several commonly discrepant items that can lead to CTC misclassification errors are outlined. Taken together, these protocols will provide a useful resource for users of this platform interested in preclinical and clinical research pertaining to metastasis and CTCs.

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