Yusa Akiko, Toneri Makoto, Masuda Taisuke, Ito Seiji, Yamamoto Shuhei, Okochi Mina, Kondo Naoto, Iwata Hiroji, Yatabe Yasushi, Ichinosawa Yoshiyuki, Kinuta Seichin, Kondo Eisaku, Honda Hiroyuki, Arai Fumihito, Nakanishi Hayao
Aichi Science and Technology Foundation, Knowledge Hub Aichi, Priority Research Projects, Japan ; Department of Micro-Nano Systems Engineering, Graduate School of Engineering, Nagoya University, Japan ; Division of Oncological Pathology, Aichi Cancer Center Research Institute, Japan.
Department of Gastrointestinal Surgery, Aichi Cancer Center Central Hospital, Japan ; Division of Oncological Pathology, Aichi Cancer Center Research Institute, Japan.
PLoS One. 2014 Feb 11;9(2):e88821. doi: 10.1371/journal.pone.0088821. eCollection 2014.
Circulating tumor cells (CTCs) in the blood of patients with epithelial malignancies provide a promising and minimally invasive source for early detection of metastasis, monitoring of therapeutic effects and basic research addressing the mechanism of metastasis. In this study, we developed a new filtration-based, sensitive CTC isolation device. This device consists of a 3-dimensional (3D) palladium (Pd) filter with an 8 µm-sized pore in the lower layer and a 30 µm-sized pocket in the upper layer to trap CTCs on a filter micro-fabricated by precise lithography plus electroforming process. This is a simple pump-less device driven by gravity flow and can enrich CTCs from whole blood within 20 min. After on-device staining of CTCs for 30 min, the filter cassette was removed from the device, fixed in a cassette holder and set up on the upright fluorescence microscope. Enumeration and isolation of CTCs for subsequent genetic analysis from the beginning were completed within 1.5 hr and 2 hr, respectively. Cell spike experiments demonstrated that the recovery rate of tumor cells from blood by this Pd filter device was more than 85%. Single living tumor cells were efficiently isolated from these spiked tumor cells by a micromanipulator, and KRAS mutation, HER2 gene amplification and overexpression, for example, were successfully detected from such isolated single tumor cells. Sequential analysis of blood from mice bearing metastasis revealed that CTC increased with progression of metastasis. Furthermore, a significant increase in the number of CTCs from the blood of patients with metastatic breast cancer was observed compared with patients without metastasis and healthy volunteers. These results suggest that this new 3D Pd filter-based device would be a useful tool for the rapid, cost effective and sensitive detection, enumeration, isolation and genetic analysis of CTCs from peripheral blood in both preclinical and clinical settings.
上皮性恶性肿瘤患者血液中的循环肿瘤细胞(CTC)为早期转移检测、治疗效果监测以及转移机制基础研究提供了一种有前景且微创的来源。在本研究中,我们开发了一种基于过滤的新型、灵敏的CTC分离装置。该装置由一个三维(3D)钯(Pd)过滤器组成,下层有一个8 µm大小的孔,上层有一个30 µm大小的凹穴,用于在通过精确光刻加电铸工艺微制造的过滤器上捕获CTC。这是一个由重力流驱动的简单无泵装置,可在20分钟内从全血中富集CTC。在装置上对CTC进行30分钟染色后,将滤盒从装置中取出,固定在盒架上,并置于直立荧光显微镜下。从一开始就对CTC进行计数和分离以进行后续基因分析,分别在1.5小时和2小时内完成。细胞加标实验表明,该Pd过滤器装置从血液中回收肿瘤细胞的回收率超过85%。通过显微操作器从这些加标的肿瘤细胞中高效分离出单个活肿瘤细胞,例如,从这种分离出的单个肿瘤细胞中成功检测到KRAS突变、HER2基因扩增和过表达。对有转移的小鼠血液进行的连续分析表明,CTC随着转移进展而增加。此外,与无转移患者和健康志愿者相比,观察到转移性乳腺癌患者血液中的CTC数量显著增加。这些结果表明,这种基于新型3D Pd过滤器的装置将是一种在临床前和临床环境中从外周血中快速、经济高效且灵敏地检测、计数、分离和基因分析CTC的有用工具。