Molecular profiling of single circulating tumor cells from lung cancer patients.
Seung-Min ParkDawson J WongChin Chun OoiDavid M KurtzOphir VermeshAmin AalipourSusie SuhKelsey L PianJacob J ChabonSang Hun LeeMehran JamaliCarmen SayJustin N CarterLuke P LeeWare G KuschnerErich J SchwartzJoseph B ShragerJoel W NealHeather A WakeleeMaximilian DiehnViswam S NairShan X WangSanjiv S GambhirPublished in: Proceedings of the National Academy of Sciences of the United States of America (2016)
Circulating tumor cells (CTCs) are established cancer biomarkers for the "liquid biopsy" of tumors. Molecular analysis of single CTCs, which recapitulate primary and metastatic tumor biology, remains challenging because current platforms have limited throughput, are expensive, and are not easily translatable to the clinic. Here, we report a massively parallel, multigene-profiling nanoplatform to compartmentalize and analyze hundreds of single CTCs. After high-efficiency magnetic collection of CTC from blood, a single-cell nanowell array performs CTC mutation profiling using modular gene panels. Using this approach, we demonstrated multigene expression profiling of individual CTCs from non-small-cell lung cancer (NSCLC) patients with remarkable sensitivity. Thus, we report a high-throughput, multiplexed strategy for single-cell mutation profiling of individual lung cancer CTCs toward minimally invasive cancer therapy prediction and disease monitoring.
Keyphrases
- circulating tumor cells
- single cell
- high throughput
- rna seq
- cancer therapy
- high efficiency
- small cell lung cancer
- circulating tumor
- minimally invasive
- end stage renal disease
- genome wide
- squamous cell carcinoma
- ejection fraction
- primary care
- drug delivery
- photodynamic therapy
- papillary thyroid
- chronic kidney disease
- dna methylation
- single molecule
- copy number
- robot assisted
- ionic liquid
- childhood cancer
- patient reported outcomes
- advanced non small cell lung cancer
- transcription factor
- liquid chromatography