From: Using single-cell sequencing technology to detect circulating tumor cells in solid tumors
Tumourtype | Cases | Blood sampling method | CTC enrichment method | CTC | Sequencing method | Analysis Sample | Target gene / sequence | Mutation type | Ref | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CTC single chipCell sorting method | Single | Primary focus | CTC | Metastases / drenchingFawn on | |||||||||
Cell Analysis number | WGA method | ||||||||||||
Mammary cancer | 15+43 | CellSave | CellSearch | DEPArray | 37+202 | Amplil™ WGAKit | qPCR/aCGH/Sanger | √ | √ | X | Erbb2/pik3ca/ allGenomic aCGH analysis | Copy number variationAnomaly / point mutation | [41] |
Mammary cancer | 2 | CellSave | CellSearch | DEPArray | 11 | Amplil™ WGAKit | Sanger | √ | √ | X | TP53 | point mutation | [7] |
Mammary cancer | 18 | CellSave | CellSearch | DEPArray | 115 | Amplil™ WGAKit | Sanger | √ | √ | X | PIK3CA | point mutation | [60] |
colorectal cancer | 6 | CellSave | CellSearch | Micromanipulation | 37 | GenomePlexSingle Cell WGA kit/ GenomiPhiDNAAmplification kit | aCGH/NGS | √ | √ | (metastases) | Whole genome aCGHAnalysis of /68 colorectal cancerGuan gene | Copy number variationAnomaly / point mutation | [35] |
colorectal cancer | 5 | CellSave | CellSearch | Micromanipulation | 69 | GenomePlexSingle Cell WGAkit | Sanger | X | √ | X | BRAF/KRAS/PIK3CA | point mutation | [6] |
Mammary cancerLung cancer | 3+2 | EDTA | CTC-Chip + doubleCoating of nanomaterialsGel matrix | frequency controlMicroabsorption | NA | NO WGA | Sanger |  √ |  √ | X | PIK3CA/EGFR | point mutation | [64] |
MalignancyPigmented tumor | 11 | Heparinized blood | Dynabeads | Laser captureMicrodissection | 14 | NO WGA | Nested PCR+ Sanger | X | √ | X | BRAF/KIT | point mutation | [61] |
Mammary cancer | 17 | EDTA | MagSweeper | Under microscopeMicro absorption | 185 | NO WGA | Nested PCR+ Sanger |  √ | √ | (metastases) | PIK3CA | point mutation | [65] |
Mammary cancer | 5 | CellSave | CellSearch | DEPArray | ≥100 | Amplil™ WGAKit | NGS | √ | √ | X | ESRI, PIK3CA>TP53 and erbB2 Point mutation; Custom Cancer Hotspot Panel v2 for Amplil WGA DNAfever | point mutation | [66] |
pancreatic cancer | 12 | ACDSolution Atubes | Dynabeads | Nano Velcro/LCM CTCChip | 222 | REPLI-g SingleCell Kit | Sanger | X | √ | X | KRAS | point mutation | [67] |
Colon cancer | 21 | EDTA | Oncoquick | DEPArray | NA | Amplil™ WGAKit | Sanger/pyrosequencing | √ | √ | X | KRAS | point mutation | [43] |
Prostatecancer | 1 | EDTA | PN-Nano Velcrochip | Laser captureMicrodissection | 25 | GenomePlexSingle Cell WGAkit | NGS | X | √ | X | Whole genome exon measurementorder | point mutation | [68] |
Prostatecancer | 1 | Anticoagulated bloodtubes | Red cell lysis + selfSlide adhesion | Micromanipulation | 41 | GenomePlexSingle Cell WGA kit | NGS | X | √ | X | whole genome sequencing | Copy number variationdifferent | [63] |
ProstateCancer / | 2 | EDTA | MagSweeper/CelISearch | Micromanipulation | 25 | MDA | NGS | √ | √ | (lymph node) | Whole genome exon measurementorder | point mutation | [8] |
lung cancer | 4 | CellSave | Cell Search | Under microscopeMicro absorption | 24 | MALBAC | NGS | √ | √ | (metastases) | Whole genome exon measurementorder | Copy number variationHetero / point mutationinsert | [9] |
Colon cancer | 2 | CellSave | CellSearch | Under microscopeMicro absorption | 5 | MALBAC | NGS | √ | √ | (lymph node) | whole genome sequencing | Copy number variationHetero / point mutationStructural variation | [62] |