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  • 1
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 73, No. 8_Supplement ( 2013-04-15), p. 5103-5103
    Abstract: Background. To isolate and quantify of CTCs, the CellSearch system is the most commonly used techniques, approved by the FDA. But in this system, EpCAM negative CTCs are excluded. To detect CTCs in malignant pleural mesothelioma patients, we have developed two novel approaches, CTC-Chip and immunomagnetic beads which could be labeled with any type of antibodies. Methods. To evaluate the accuracy of the number of CTCs, we used the peripheral blood samples collected from healthy donors, spiked definite number of tumor cell lines, ACC-MESO1 and ACC-MESO4. Both tumor cell lines (obtained from ATCC) were derived from malingnant pleural mesothelioma, positive of mesothelin and podoplanin. The recovery rate was evaluated with two methods, the CTC-Chip and immunomagnetic beads, coated with antibodies specific for mesothelin and podoplanin. In addition, an 8 ml sample of peripheral blood was collected from a patient with malignant pleural mesothelioma, and was served for the immunomagnetic beads. To identify the captured cells as tumor cells, immunocytochemistry was performed using with the cocktail of two human cytokeratin-specific antibodies. Results. To confirm the efficacy of tumor isolation by two methods, we used tumor cell suspicion as samples. In CTC-Chip coated with anti-mesothelin and podoplanin, the recovery rate of captured ACC-MESO1 was 99%, 97%, respectively. The recovery efficiency of ACC-MESO1-spiked blood samples using CTC-Chip coated with anti-mesothelin and podoplanin, was 45%, 80%, respectively. In immunomagnetic beads coated with anti-mesothelin and podoplanin, the recovery rate of captured ACC-MESO4 was 80%, 25%, respectively. The recovery efficiency of ACC-MESO4-spiked blood samples using immunomagnetic beads coated with anti-mesothelin and podoplanin, was 33%, 15%, respectively. The CTCs from a patient was detected using with immunomagnetic beads coated with anti-mesothelin antibody and CTC count was 440 per 8 ml of peripheral blood. Conclusions. Both CTC-Chip and immunomagnetic beads could capture CTCs, using antibodies specific for mesothelin and podoplanin. Detection of CTCs from a patient with malignant pleural mesothelioma was performed by labeling of mesothelin-coated immunomagnetic beads. But the recovery rate of tumor cells in spiked samples were less than 30%. The step of deletion of red blood cells is necessary to be improved. Citation Format: Chikaishi Yasuhiro, Tomoko So, Soichi Oka, Masaru Takenaka, Makoto Nakagawa, Hidehiko Shimokawa, Teruo Iwata, Yoshika Nagata, Hidetaka Uramoto, Takeshi Hanagiri, Takeshi Ohnaga, Fumihiro Tanaka. Development of detecting systems for circulating tumor cells in malignant pleural mesothelioma patients. [abstract]. In: Proceedings of the 104th Annual Meeting of the American Association for Cancer Research; 2013 Apr 6-10; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2013;73(8 Suppl):Abstract nr 5103. doi:10.1158/1538-7445.AM2013-5103
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
    RVK:
    RVK:
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2013
    detail.hit.zdb_id: 2036785-5
    detail.hit.zdb_id: 1432-1
    detail.hit.zdb_id: 410466-3
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  • 2
    In: Oncology Letters, Spandidos Publications, ( 2017-12-20)
    Type of Medium: Online Resource
    ISSN: 1792-1074 , 1792-1082
    Language: Unknown
    Publisher: Spandidos Publications
    Publication Date: 2017
    detail.hit.zdb_id: 2573196-8
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  • 3
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 74, No. 19_Supplement ( 2014-10-01), p. 3080-3080
    Abstract: Background. The CellSearch system is the most commonly used technique approved by the FDA to isolate and quantify circulation tumor cells (CTCs). However, in this system, the efficiency of CTC isolation is influenced by the epithelial cell adhesion molecule (EpCAM). Therefore, it is difficult to isolate CTCs in the setting of the epithelial to mesenchymal transition (EMT), malignant pleural mesothelioma and so on. We developed polymeric microfluidic devices for CTC isolation (CTC-chip) and compared the efficacy of CellSearch with CTC-chip using EpCAM-negative tumor cell lines of malignant pleural mesothelioma. Methods. In order to evaluate the accuracy of the number of CTCs, we used PBS samples and peripheral blood samples (blood samples) collected from healthy donors to which spiking the tumor cell lines ACC-MESO1 and ACC-MESO4. Both tumor cell lines (obtained from ATCC) were derived from malignant pleural mesothelioma, positive for mesothelin and podoplanin and negative for EpCAM. The recovery rate was evaluated using two methods. CellSearch was performed according to the normal method, while CTC-chip was performed using a two coating pattern with anti-mesothelin antibody (chip1) and anti-podoplanin antibody (chip2). Results. In the PBS samples, the recovery rate of captured ACC-MESO1 was 8.6%/98%/99% (CellSearch/chip 1/chip 2), while those of ACC-MESO4 was 21.1%/97%/99%, respectively. In the blood samples, the recovery rate of captured ACC-MESO1 was 1.2%/6.2%/13.3% (CellSearch/chip 1/chip 2), while that of ACC-MESO4 was 6.0%/3.7%/11.6%, respectively. Conclusions. Our experiments showed that the recovery rate of each sample was higher using CTC-chip than that obtained with CellSearch. Moreover, CTC-chip coated anti-podoplanin antibody exhibited a higher recovery rate than coated anti-mesothelin antibody. Future studies using experiments of CTC isolation in cancer patients with malignant pleural mesothelioma are thus required. Citation Format: Yasuhiro Chikaishi, Tomoko So, Masaru Takenaka, Soichi Oka, Ayako Hirai, Takashi Iwanami, Hidehiko Shimokawa, Kazue Yoneda, Yoshika Nagata, Hidetaka Uramoto, Takeshi Ohnaga, Fumihiro Tanaka. Comparison of CellSearch with polymeric microfluidic devices for CTC isolation using EpCAM-negative tumor cell lines of malignant pleural mesothelioma. [abstract]. In: Proceedings of the 105th Annual Meeting of the American Association for Cancer Research; 2014 Apr 5-9; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2014;74(19 Suppl):Abstract nr 3080. doi:10.1158/1538-7445.AM2014-3080
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
    RVK:
    RVK:
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2014
    detail.hit.zdb_id: 2036785-5
    detail.hit.zdb_id: 1432-1
    detail.hit.zdb_id: 410466-3
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