A Modified and Convenient Method for Assessing Tumor Cell Invasion and Migration and Its Application to Screening for Inhibitors
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概要
- 論文の詳細を見る
In order to screen potent inhibitors of tumor invasion and metastasis, we here devised a simple and reproducible in vitro assay for tumor invasion and migration. A conventional cell-counting assay using a Transwell chamber with a microporous membrane filter is troublesome and time-consuming, involving visually counting the cells under a microscope, and the invaded or migrated cells are sometimes distributed unevenly in predetermined fields on the lower surface of the filter. Therefore, it is difficult to evaluate the invasive and migratory abilities of tumor cells easily and quantitatively by the cell counting method. In the present study, crystal violet dye was used for staining the invaded cells and colorimetrically assessing the invasive ability per filter as an absorbance. In this crystal violet assay, tumor cell invasion into a reconstituted basement membrane Matrigel was proportional to both the cell number added into the chamber and the incubation period, and inversely proportional to the amount of Matrigel barrier on the upper surface of filter. The results obtained by this dye-uptake method were highly consistent with those of a conventional cell-counting assay. Using this crystal violet assay, the anti-invasive effect of doxorubicin (DOX) was detected more easily and found to be highly proportional to that by the conventional cell-counting method. We therefore applied this convenient assay method to screen anti-invasive and anti-metastatic compounds. As a result, caffeic acid was found to be more active in the inhibition of both tumor cell invasion and migration without showing direct cytotoxicity in vitro than other related compounds.
- 公益社団法人日本薬学会の論文
- 1997-04-15
著者
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SAIKI Ikuo
Department of Pathogenic Biochemistry, Institute of Natural Medicine, Toyama Medical and Pharmaceuti
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Saiki Ikuo
Department Of Pathogenic Biochemistry Research Institute For Wakan-yaku (traditional Sino-japanese M
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Saiki Ikuo
Department Of Pathological Biochemistry Institute Of Natural Medicine Toyama Medical And Pharmaceuti
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Hattori Masao
Department Of Metabolic Engineering Institute Of Natural Medicine Toyama Medical And Pharmaceutical
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SAITO Ken-ichi
Department of Kampo Medicinal Science, Hokkaido College of Pharmacy
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OKU Tohru
Department of Physiology Osaka Medical College
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Oku Teruaki
Department Of Microbiology Hoshi University School Of Pharmacy And Pharmaceutical Sciences
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Oku Teruaki
Department Of Microbiology School Of Pharmacy Hoshi University
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ATA Naomi
Department of Pathogenic Biochemistry, Research Institute for Wakan-Yaku (Traditional Sino-Japanese
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Hattori Masao
Department Of Cell-resources Engineering Research Institute For Wakan-yaku (traditional Sino-japanes
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済木 育夫
Department Of Pathogenic Biochemistry Institute Of Natural Medicine Toyama Medical And Pharmaceutica
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MIYASHIRO Hirotsugu
Department of Cell-Resources Engineering, Research Institute for Wakan-Yaku (Traditional Sino-Japane
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Ata Naomi
Department Of Pathogenic Biochemistry Research Institute For Wakan-yaku (traditional Sino-japanese M
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Oku T
Amagasaki Chemical Industries Co.
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Saiki Ikuo
Department Of Pathogenic Biochemistry Institute Of Natural Medicine Toyama Medical And Pharmaceutica
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Miyashiro Hirotsugu
Department Of Cell-resources Engineering Research Institute For Wakan-yaku (traditional Sino-japanes
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Saiki Ikuo
Department Of Bioscience Institute Of Natural Medicine Toyama University
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Saito Ken-ichi
Department Of Pathogenic Biochemistry Research Institute For Wakan-yaku (traditional Sino-japanese M
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