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蜂胶提取物对HeLa细胞及其耐药亚系化疗药物敏感性的影响。

Effects of propolis extract on sensitivity to chemotherapeutic agents in HeLa and resistant sublines.

作者信息

Takara Kohji, Fujita Megumi, Matsubara Mika, Minegaki Tetsuya, Kitada Noriaki, Ohnishi Noriaki, Yokoyama Teruyoshi

机构信息

Department of Hospital Pharmacy, Faculty of Pharmaceutical Sciences, Kyoto Pharmaceutical University, 5 Nakauchi-cho, Misasagi, Yamashina-ku, Kyoto 607-8414, Japan.

出版信息

Phytother Res. 2007 Sep;21(9):841-6. doi: 10.1002/ptr.2165.

Abstract

The effects of a propolis extract obtained by supercritical fluid extraction on sensitivity to chemotherapeutic agents were examined in HeLa cells and resistant sublines thereof. In addition, the actions of propolis and caffeic acid phenethyl ester (CAPE), a constituent of propolis, on the multidrug efflux transporter P-glycoprotein/MDR1, were evaluated in paclitaxel-resistant HeLa/TXL cells (MDR1-overexpressing cells). In HeLa cells, the sensitivity to paclitaxel and doxorubicin, substrates of MDR1, was unchanged in the presence of propolis. In HeLa/TXL cells, propolis increased sensitivity to these MDR1 substrates. The accumulation of Rhodamine123, also a substrate for MDR1, by HeLa/TXL cells increased in the presence of 50 microg/mL, but not 10 microg/mL, of the extract. However, the growth inhibition of HeLa/TXL cells by paclitaxel was not changed by CAPE, although the accumulation of Rhodamine123 increased significantly in the presence of 100 microm, but not 1 nM or 1 microm, CAPE. Collectively, the extract was suggested to inhibit the function of MDR1 and to increase the sensitivity to MDR1 substrates in HeLa/TXL cells, effects likely to be caused by constituents other than CAPE.

摘要

研究了通过超临界流体萃取获得的蜂胶提取物对HeLa细胞及其耐药亚系对化疗药物敏感性的影响。此外,在耐紫杉醇的HeLa/TXL细胞(MDR1过表达细胞)中评估了蜂胶及其成分咖啡酸苯乙酯(CAPE)对多药外排转运蛋白P-糖蛋白/MDR1的作用。在HeLa细胞中,在蜂胶存在的情况下,对MDR1底物紫杉醇和阿霉素的敏感性没有变化。在HeLa/TXL细胞中,蜂胶增加了对这些MDR1底物的敏感性。在50μg/mL(而非10μg/mL)提取物存在的情况下,HeLa/TXL细胞对同样是MDR1底物的罗丹明123的摄取增加。然而,尽管在100μM(而非1nM或1μM)CAPE存在时罗丹明123的摄取显著增加,但CAPE并未改变紫杉醇对HeLa/TXL细胞的生长抑制作用。总体而言,该提取物被认为可抑制HeLa/TXL细胞中MDR1的功能并增加对MDR1底物的敏感性,这些作用可能是由CAPE以外的成分引起的。

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