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体外研究人乳腺癌和黑色素瘤细胞系对源自芥末的6-(甲基亚磺酰基)己基异硫氰酸酯的选择性敏感性。

Selective sensitivity to wasabi-derived 6-(methylsulfinyl)hexyl isothiocyanate of human breast cancer and melanoma cell lines studied in vitro.

作者信息

Nomura Takahiro, Shinoda Shoko, Yamori Takao, Sawaki Saeko, Nagata Ikuko, Ryoyama Kazuo, Fuke Yoko

机构信息

Division of Food and Nutritional Science, Kanazawa Gakuin College, 10 Sue-machi, Kanazawa, Ishikawa 920-1392, Japan.

出版信息

Cancer Detect Prev. 2005;29(2):155-60. doi: 10.1016/j.cdp.2004.07.010.

Abstract

Recently, attention has focused on the anticancer properties of an aromatic component 6-(methylsulfinyl)hexyl isothiocyanate (6-MITC) in a typical Japanese spice, wasabi. In this paper, anticancer activity of 6-MITC in vitro was studied by using a human cancer cell (HCC) panel. 6-MITC directly affected the cells in the HCC panel and inhibited their growth in culture. The mean concentration required to inhibit 50% of control cell growth was 3.9 microM, which is a sufficiently low dosage for practical use. The suppression influenced not only the cell growth, but also the survival of these cells. The mean concentration to suppress cells to a 50% survival was 43.7 microM. The reduction activity of 6-MITC was differential, and it suppressed specific cells. These severely suppressed cell lines included breast cancer and melanoma cell lines. For example, one melanoma line was seriously damaged at a concentration of 0.3 microM of 6-MITC. Compared with other MITCs (2-MITC, 4-MITC and 8-MITC), 6-MITC showed the most effective suppression and with the most specific manner of the cells mentioned above. A "COMPARE" analysis using a computerized algorithm, which was based on the HCC database, suggested that the suppression mechanism of 6-MITC is unique and may be different from that of other known chemicals. The actual mechanism may not a simple one but may involve multiple pathways. On account of its sufficiently small size, 6-MITC is a new possible candidate for controlling cancer cells.

摘要

最近,人们的注意力集中在一种典型的日本香料山葵中的芳香成分6-(甲基亚磺酰基)己基异硫氰酸酯(6-MITC)的抗癌特性上。在本文中,通过使用人类癌细胞(HCC)面板研究了6-MITC的体外抗癌活性。6-MITC直接影响HCC面板中的细胞并抑制其在培养中的生长。抑制对照细胞生长50%所需的平均浓度为3.9 microM,这是一个在实际应用中足够低的剂量。这种抑制不仅影响细胞生长,还影响这些细胞的存活。将细胞存活率抑制到50%的平均浓度为43.7 microM。6-MITC的还原活性具有差异性,它能抑制特定的细胞。这些被严重抑制的细胞系包括乳腺癌和黑色素瘤细胞系。例如,一种黑色素瘤细胞系在6-MITC浓度为0.3 microM时受到严重损伤。与其他MITC(2-MITC、4-MITC和8-MITC)相比,6-MITC对上述细胞的抑制效果最有效且方式最具特异性。使用基于HCC数据库的计算机算法进行的“COMPARE”分析表明,6-MITC的抑制机制是独特的,可能与其他已知化学物质不同。实际机制可能不是单一的,而是可能涉及多种途径。由于其尺寸足够小,6-MITC是控制癌细胞的一种新的可能候选物。

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