He Wei, Wang Haifeng, Hartmann Lynn C, Cheng Ji-Xin, Low Philip S
Department of Chemistry, Purdue University, West Lafayette, IN 47907, USA.
Proc Natl Acad Sci U S A. 2007 Jul 10;104(28):11760-5. doi: 10.1073/pnas.0703875104. Epub 2007 Jun 29.
Quantitation of circulating tumor cells (CTCs) constitutes an emerging tool for the diagnosis and staging of cancer, assessment of response to therapy, and evaluation of residual disease after surgery. Unfortunately, no existing technology has the sensitivity to measure the low numbers of tumor cells (<1 CTC per ml of whole blood) that characterize minimal levels of disease. We present a method, intravital flow cytometry, that noninvasively counts rare CTCs in vivo as they flow through the peripheral vasculature. The method involves i.v. injection of a tumor-specific fluorescent ligand followed by multiphoton fluorescence imaging of superficial blood vessels to quantitate the flowing CTCs. Studies in mice with metastatic tumors demonstrate that CTCs can be quantitated weeks before metastatic disease is detected by other means. Analysis of whole blood samples from cancer patients further establishes that human CTCs can be selectively labeled and quantitated when present at approximately 2 CTCs per ml, opening opportunities for earlier assessment of metastatic disease.
循环肿瘤细胞(CTC)的定量分析是一种新兴的工具,可用于癌症的诊断和分期、评估治疗反应以及评估手术后的残留疾病。不幸的是,目前没有现有技术能够灵敏地检测到表征疾病最低水平的少量肿瘤细胞(每毫升全血中<1个CTC)。我们提出了一种方法,即活体流式细胞术,该方法可以在罕见的CTC流经外周脉管系统时对其进行无创体内计数。该方法包括静脉注射肿瘤特异性荧光配体,然后对浅表血管进行多光子荧光成像以定量流动的CTC。对患有转移性肿瘤的小鼠的研究表明,在通过其他方法检测到转移性疾病前数周就能对CTC进行定量分析。对癌症患者全血样本的分析进一步证实,当每毫升血液中约有2个CTC时,人类CTC可以被选择性标记和定量,这为更早地评估转移性疾病提供了机会。