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Continuous centrifugal microfluidics (CCM) isolates heterogeneous circulating tumor cells via full automation

Understanding cancer heterogeneity is essential to finding diverse genetic mutations in metastatic cancers. Thus, it is critical to isolate all types of CTCs to identify accurate cancer information from patients. Moreover, full automation robustly capturing the full spectrum of CTCs is an urgent nee...

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Detalles Bibliográficos
Autores principales: Woo, Hyeong Jung, Kim, Seung-Hoon, Kang, Hyo Jung, Lee, Soo-Hwan, Lee, Seung Joon, Kim, Jong Man, Gurel, Ogan, Kim, Soo Yeol, Roh, Hye Ran, Lee, Jungmin, Park, Yeonsoo, Shin, Hyun Young, Shin, Yong-Il, Lee, Sun Min, Oh, So Yeon, Kim, Young Zoon, Chae, Jung-Il, Lee, Seoyoung, Hong, Min Hee, Cho, Byoung Chul, Lee, Eun Sook, Pantel, Klaus, Kim, Hye Ryun, Kim, Minseok S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9131262/
https://www.ncbi.nlm.nih.gov/pubmed/35664056
http://dx.doi.org/10.7150/thno.72511
Descripción
Sumario:Understanding cancer heterogeneity is essential to finding diverse genetic mutations in metastatic cancers. Thus, it is critical to isolate all types of CTCs to identify accurate cancer information from patients. Moreover, full automation robustly capturing the full spectrum of CTCs is an urgent need for CTC diagnosis to be routine clinical practice. Methods: Here we report the full capture of heterogeneous CTC populations using fully automated, negative depletion-based continuous centrifugal microfluidics (CCM). Results: The CCM system demonstrated high performance (recovery rates exceeding 90% and WBC depletion rate of 99.9%) across a wide range of phenotypes (EpCAM(+), EpCAM(-), small-, large-sized, and cluster) and cancers (lung, breast, and bladder). Applied in 30 lung adenocarcinoma patients harboring epidermal growth factor receptor (EGFR) mutations, the system isolated diverse phenotypes of CTCs in marker expression and size, implying the importance of unbiased isolation. Genetic analyses of intra-patient samples comparing cell-free DNA with CCM-isolated CTCs yielded perfect concordance, and CTC enumeration using our technique was correlated with clinical progression as well as response to EGFR inhibitors. Conclusion: Our system also introduces technical advances which assure rapid, reliable, and reproducible results, thus enabling a more comprehensive application of robust CTC analysis in clinical practice.