Verification of A New Filter for Isolation of Circulating Tumor Cells by Only Blood Filtration

被引:5
作者
Morita, Kohei [1 ,2 ]
Sawabata, Noriyoshi [3 ,9 ]
Tatsumi, Shigenobu [4 ]
Fujii, Tomomi [1 ]
Nishikawa, Takashi [4 ]
Kawaguchi, Takeshi [3 ]
Arakane, Toru [5 ]
Tominaga, Yoshiaki [5 ]
Sakaguchi, Hirokazu [5 ]
Kobayashi, Taro [6 ]
Hontsu, Shigeto [7 ]
Yamamoto, Yoshifumi [7 ]
Fujioka, Nobuhiro [7 ]
Ouji-sageshima, Noriko [8 ]
Ito, Toshihiro [8 ]
Ohbayashi, Chiho [1 ]
机构
[1] Nara Med Univ, Dept Diagnost Pathol, Sch Med, Kashihara, Japan
[2] Nara Prefecture Gen Med Ctr, Dept Diagnost Pathol, Nara, Japan
[3] Nara Med Univ, Dept Thorac & Cardio Vasc Surg, Sch Med, Kashihara, Japan
[4] Nara Med Univ Hosp, Dept Pathol & Diag, Kashihara, Japan
[5] Toray Industries Ltd, Tokyo, Japan
[6] Ikeda Sci Co Ltd, Tokyo, Japan
[7] Nara Med Univ, Dept Resp Med, Sch Med, Kashihara, Japan
[8] Nara Med Univ, Dept Immunol, Sch Med, Kashihara, Japan
[9] Nara Med Univ, Dept Thorac & Cardio Vasc Surg, 840 Shijo Cho Kashihara, Nara 6348522, Japan
关键词
Circulating tumor cells; filter; Immunostaining; cell culture; gene mutation analysis; SIZE;
D O I
10.21873/anticanres.15930
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: Since circulating tumor cells (CTCs) are precursors of metastatic lesions, extracting CTCs from whole blood is useful in obtaining information for cancer treatment. One of the CTC isolation methods is the size selection method; however, since the conventional methods are expensive and cumbersome, we developed an affordable and simple filter, whose usefulness is verified in this study. Materials and Methods: The new filter [hereafter, soft micropore filter (S-MPF)] is made up of a polyethylene film with a thickness of 15 ,um and conical pores having a diameter of 8-10 ,um, which are opened uniformly (opening rate, 20%). This filter can filter whole blood by free-falling under gravity. The possibilities of the filter's usage for model CTC isolation, immunostaining, short-term cell culture, and gene mutation detection in extracted model CTCs were verified. Results: S-MPF was able to extract model CTCs with an isolation rate of up to 15%. These model CTCs were detected by cytology, immunostaining, and culture by short-term incubation of filtered cells. Furthermore, genetic mutations were identified in the cultured cells. In addition, CTC isolation from the peripheral blood of patients with lung cancer was demonstrated by setting the volume of collected blood to 15 ml to prevent a low recovery rate. Conclusion: The S-MPF can be used to extract model CTCs quickly and easily. Moreover, cytological diagnosis, immunostaining, short-term culture, and gene mutation search are possible with this filter. Given its proven applicability in clinical samples, this filter can be used in clinical settings.
引用
收藏
页码:4305 / 4310
页数:6
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