4.7 Article

High-density single cell mRNA sequencing to characterize circulating tumor cells in hepatocellular carcinoma

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SCIENTIFIC REPORTS
卷 8, 期 -, 页码 -

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NATURE PORTFOLIO
DOI: 10.1038/s41598-018-30047-y

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资金

  1. American Association for the Study of Liver Diseases Foundation (AASLDF) Alan Hofmann Clinical and Translational Research Award
  2. U.S. Department of Defense [CA150272P3]
  3. Tisch Cancer Institute [P30 CA196521]
  4. National Cancer Institute Ruth L. Kirschstein NRSA Institutional Research Training Grant [CA078207]
  5. Swiss National Science Foundation
  6. Foundation Roberto Gianna Gonella
  7. Foundation SICPA
  8. Spanish Association for the Study of the Liver (Asociacion Espanola para el Estudio del Higado, AEEH)
  9. Cancer Research Grant from NuovoSoldati Foundation
  10. Deutsche Forschungsgemeinschaft (German Research Foundation)
  11. PRIME (Program for Research on Immune Modeling and Experimentation), an NIAID [U19 AI117873]

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Patients with hepatocellular carcinoma (HCC) release tumor cells to the bloodstream, which can be detected using cell surface markers. Despite numerous reports suggest a direct correlation between the number of circulating tumor cells (CTCs) and poor clinical outcomes, few studies have provided a thorough molecular characterization of CTCs. Due to the limited access to tissue samples in patients at advanced stages of HCC, it is crucial to develop new technologies to identify HCC cancer drivers in routine clinical conditions. Here, we describe a method that sequentially combines image flow cytometry and high density single-cell mRNA sequencing to identify CTCs in HCC patients. Genome wide expression profiling of CTCs using this approach demonstrates CTC heterogeneity and helps detect known oncogenic drivers in HCC such as IGF2. This integrated approach provides a novel tool for biomarker development in HCC using liquid biopsy.

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