Genetic analysis of circulating tumor cells in pancreatic cancer patients: A pilot study

被引:14
|
作者
Goerner, Karin [1 ]
Bachmann, Jeannine [2 ]
Holzhauer, Claudia [1 ]
Kirchner, Roland [1 ]
Raba, Katharina [4 ]
Fischer, Johannes C. [4 ]
Martignoni, Marc E. [2 ]
Schiemann, Matthias [3 ]
Alunni-Fabbroni, Marianna [1 ]
机构
[1] Beckman Coulter Biomed GmbH, D-81377 Munich, Germany
[2] Tech Univ Munich, Dept Surg, Klinikum Rechts Isar, D-81675 Munich, Germany
[3] Tech Univ Munich, Inst Med Microbiol Immunol & Hyg, D-81675 Munich, Germany
[4] Univ Dusseldorf, Inst Transplantat Diagnost & Cell Therapy, Fac Med, D-40225 Dusseldorf, Germany
关键词
Circulating tumor cells; Flow cytometry; Genetic profile; Pancreatic cancer; RT-PCR; METASTATIC BREAST-CANCER; PERIPHERAL-BLOOD; PROGNOSTIC-FACTOR; LIQUID BIOPSY; CHEMOTHERAPY; PROGRESSION; SIZE;
D O I
10.1016/j.ygeno.2015.02.003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Pancreatic cancer is one of the most aggressive malignant tumors, mainly due to an aggressive metastasis spreading. In recent years, circulating tumor cells became associated to tumor metastasis. Little is known about their expression profiles. The aim of this study was to develop a complete workflow making it possible to isolate circulating tumor cells from patients with pancreatic cancer and their genetic characterization. Results: We show that the proposedworkflow offers a technical sensitivity and specificity high enough to detect and isolate single tumor cells. Moreover our approach makes feasible to genetically characterize single CTCs. Conclusions: Our work discloses a complete workflow to detect, count and genetically analyze individual CTCs isolated from blood samples. This method has a central impact on the early detection of metastasis development. The combination of cell quantification and genetic analysis provides the clinicians with a powerful tool not available so far. (C) 2015 Published by Elsevier Inc.
引用
收藏
页码:7 / 14
页数:8
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