Isolation of rare circulating tumour cells in cancer patients by microchip technology

被引:2926
作者
Nagrath, Sunitha
Sequist, Lecia V.
Maheswaran, Shyamala
Bell, Daphne W.
Irimia, Daniel
Ulkus, Lindsey
Smith, Matthew R.
Kwak, Eunice L.
Digumarthy, Subba
Muzikansky, Alona
Ryan, Paula
Balis, Ulysses J.
Tompkins, Ronald G.
Haber, Daniel A.
Toner, Mehmet [1 ]
机构
[1] Harvard Univ, Sch Med, Surg Serv, Massachusetts Gen Hosp, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, BioMEMS Resource Ctr, Massachusetts Gen Hosp, Boston, MA 02114 USA
[3] Shriners Hosp Children, Boston, MA 02114 USA
[4] Harvard Univ, Sch Med, Massachusetts Gen Hosp Canc Ctr, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nature06385
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Viable tumour- derived epithelial cells ( circulating tumour cells or CTCs) have been identified in peripheral blood from cancer patients and are probably the origin of intractable metastatic disease(1-4). Although extremely rare, CTCs represent a potential alternative to invasive biopsies as a source of tumour tissue for the detection, characterization and monitoring of non-haematologic cancers(5-8). The ability to identify, isolate, propagate and molecularly characterize CTC subpopulations could further the discovery of cancer stem cell biomarkers and expand the understanding of the biology of metastasis. Current strategies for isolating CTCs are limited to complex analytic approaches that generate very low yield and purity(9). Here we describe the development of a unique microfluidic platform ( the 'CTC-chip') capable of efficient and selective separation of viable CTCs from peripheral whole blood samples, mediated by the interaction of target CTCs with antibody ( EpCAM)- coated microposts under precisely controlled laminar flow conditions, and without requisite pre- labelling or processing of samples. The CTC- chip successfully identified CTCs in the peripheral blood of patients with metastatic lung, prostate, pancreatic, breast and colon cancer in 115 of 116 ( 99%) samples, with a range of 5-1,281 CTCs per ml and approximately 50% purity. In addition, CTCs were isolated in 7/7 patients with early- stage prostate cancer. Given the high sensitivity and specificity of the CTC- chip, we tested its potential utility in monitoring response to anti- cancer therapy. In a small cohort of patients with metastatic cancer undergoing systemic treatment, temporal changes in CTC numbers correlated reasonably well with the clinical course of disease as measured by standard radiographic methods. Thus, the CTC- chip provides a new and effective tool for accurate identification and measurement of CTCs in patients with cancer. It has broad implications in advancing both cancer biology research and clinical cancer management, including the detection, diagnosis and monitoring of cancer(10).
引用
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页码:1235 / U10
页数:7
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