Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/35108
標題: Reversal of doxorubicin resistance in breast cancer cells by photochemical internalization
作者: Lou, P.J.
賴秉杉
Lai, P.S.
Shieh, M.J.
MacRobert, A.J.
Bergs, K.
Bown, S.G.
關鍵字: photodynamic therapy
photochemical internalization
doxorubicin
resistant breast cancer cells
cationic photosensitizing agent
mediated photodynamic therapy
multidrug-resistance
confocal microscopy
tumor-cells
chemotherapy
combination
adriamycin
daunorubicin
transporter
期刊/報告no:: International Journal of Cancer, Volume 119, Issue 11, Page(s) 2692-2698.
摘要: Multiple drug resistance (MDR) is a problem that seriously reduces the efficacy of many chemotherapy agents. One mechanism for MDR is increased acidification of endocytic vesicles and increased cytosol pH, so weak base chemotherapeutic agents, including doxorubicin, are trapped in endocytic vesicles and exhibit a drug resistant phenotype. Treatments that selectively reverse this accumulation may therefore reverse the MDR phenotype. Photochemical internalization (PCI) is a novel technology developed for site-specific enhancement of the therapeutic efficacy of macromolecules by selective photochemical rupture of endocytic vesicles and consequent release of endocytosed macromolecules into the cytosol. This study evaluates PCI for release of doxorubicin from endocytic vesicles in MDR cells. Two breast cancer cell lines, MCF-7 and MCF-7/ADR (the latter resistant to doxorubicin), were selected. They were found equally sensitive to photochemical treatment with the photosensitiser TPPS(2a) (disulfonated meso-tetraphenylporphine) and light. On exposure to doxorubicin alone, the IC(50) (drug concentration for 50% reduction in colony formation) was 0.1 mu M for MCF-7 and 1 mu M for MCF-7/ADR. After PCI (photochemical treatment followed by doxorubicin), the IC(50) concentration was 0.1 mu M for both cell lines. Comparable changes were seen with assay of cell viability using 3-(4,5-dime- thyltiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT). On fluorescence microscopy in MCF-7/ADR cells, doxorubicin localised in granules identified as lysosomes. After PCI, doxorubicin was released into the cytosol and entered cell nuclei, as was seen in MCF-7 cells without PCI. In conclusion, PCI reversed the MDR phenotype of doxorubicin resistant breast cancer cells by endo-lysosomal release of the drug. The technique is a promising new approach to tackling the problem of MDR. (c) 2006 Wiley-Liss, Inc.
URI: http://hdl.handle.net/11455/35108
ISSN: 0020-7136
文章連結: http://dx.doi.org/10.1002/ijc.22098
Appears in Collections:化學系所

文件中的檔案:

取得全文請前往華藝線上圖書館



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.