Tumor cell-based liquid biopsy using high-throughput microfluidic enrichment of entire leukapheresis product.
Avanish MishraShih-Bo HuangTaronish DubashRisa BurrJon F EddBen S WittnerQuinn E CunneelyVictor R PutaturoAkansha DeshpandeEzgi AntmenKaustav A GopinathanKeisuke OtaniYoshiyuki MiyazawaJi Eun KwakSara Y GuayJustin KellyJohn WalshLinda NiemanIsabella GallerPuiYee ChanMichael S LawrenceRyan J SullivanAditya BardiaDouglas S MicalizziLecia V SequistRichard J LeeJoseph W FransesDavid T TingPatricia A R BrunkerShyamala MaheswaranDavid T MiyamotoDaniel A HaberMehmet TonerPublished in: bioRxiv : the preprint server for biology (2024)
Circulating Tumor Cells (CTCs), interrogated by sampling blood from patients with cancer, contain multiple analytes, including intact RNA, high molecular weight DNA, proteins, and metabolic markers. However, the clinical utility of tumor cell-based liquid biopsy has been limited since CTCs are very rare, and current technologies cannot process the blood volumes required to isolate a sufficient number of tumor cells for in-depth assays. We previously described a high-throughput microfluidic prototype utilizing high-flow channels and amplification of cell sorting forces through magnetic lenses. Here, we apply this technology to analyze patient-derived leukapheresis products, interrogating a mean blood volume of 5.83 liters from patients with metastatic cancer, with a median of 2,799 CTCs purified per patient. Isolation of many CTCs from individual patients enables characterization of their morphological and molecular heterogeneity, including cell and nuclear size and RNA expression. It also allows robust detection of gene copy number variation, a definitive cancer marker with potential diagnostic applications. High-volume microfluidic enrichment of CTCs constitutes a new dimension in liquid biopsies.
Keyphrases
- circulating tumor cells
- single cell
- high throughput
- circulating tumor
- copy number
- cell therapy
- mitochondrial dna
- poor prognosis
- nucleic acid
- papillary thyroid
- ultrasound guided
- end stage renal disease
- genome wide
- newly diagnosed
- young adults
- risk assessment
- high resolution
- optical coherence tomography
- prognostic factors
- quantum dots
- climate change
- genome wide analysis
- childhood cancer