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Reduced cellular glutathione levels do not affect the cytotoxicity or photocytotoxicity of the cationic photosensitiser Victoria Blue BO.细胞内谷胱甘肽水平降低并不影响阳离子光敏剂维多利亚蓝BO的细胞毒性或光细胞毒性。
Membr Cell Biol. 2000;14(3):357-66.
2
Cytotoxicity and adjuvant activity of cationic photosensitizers in a multidrug resistant cell line.阳离子光敏剂在多药耐药细胞系中的细胞毒性及佐剂活性
J Chemother. 1999 Feb;11(1):61-8. doi: 10.1179/joc.1999.11.1.61.
3
A critical evaluation of the mechanisms of action proposed for the antitumor effects of the anthracycline antibiotics adriamycin and daunorubicin.对蒽环类抗生素阿霉素和柔红霉素抗肿瘤作用所提出的作用机制的批判性评价。
Biochem Pharmacol. 1999 Apr 1;57(7):727-41. doi: 10.1016/s0006-2952(98)00307-4.
4
Characterization of acidic vesicles in multidrug-resistant and sensitive cancer cells by acridine orange staining and confocal microspectrofluorometry.通过吖啶橙染色和共聚焦显微光谱荧光测定法对多药耐药和敏感癌细胞中的酸性囊泡进行表征。
J Histochem Cytochem. 1997 Sep;45(9):1255-64. doi: 10.1177/002215549704500909.
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Localization of anthracycline accumulation in sensitive and resistant urothelial tumor cell lines.
Cancer Detect Prev. 1996;20(6):625-33.
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Determination and reversal of resistance to epirubicin intravesical chemotherapy. A confocal imaging study.
Br J Urol. 1996 Jun;77(6):824-9. doi: 10.1046/j.1464-410x.1996.09539.x.
7
Defective pH regulation of acidic compartments in human breast cancer cells (MCF-7) is normalized in adriamycin-resistant cells (MCF-7adr).人乳腺癌细胞(MCF-7)中酸性区室的pH调节缺陷在阿霉素耐药细胞(MCF-7adr)中恢复正常。
Biochemistry. 1996 Mar 5;35(9):2811-7. doi: 10.1021/bi952234e.
8
Nuclear immunolocalization of P-glycoprotein in multidrug-resistant cell lines showing similar mechanisms of doxorubicin distribution.多药耐药细胞系中P-糖蛋白的核免疫定位显示阿霉素分布机制相似。
Eur J Cell Biol. 1995 Nov;68(3):226-39.
9
Choline phospholipids: signal transduction and carcinogenesis.胆碱磷脂:信号转导与致癌作用
FASEB J. 1993 Apr 1;7(6):551-7. doi: 10.1096/fasebj.7.6.8472893.
10
Role of anionic phospholipids in the interaction of doxorubicin and plasma membrane vesicles: drug binding and structural consequences in bacterial systems.阴离子磷脂在阿霉素与质膜囊泡相互作用中的作用:细菌系统中的药物结合及结构影响
Biochemistry. 1993 Jul 6;32(26):6688-95. doi: 10.1021/bi00077a023.

使用共聚焦显微镜研究阿霉素和维多利亚蓝 BO 在 EMT6-S 和 EMT6-R 细胞中的细胞内定位。

Intracellular localisation studies of doxorubicin and Victoria Blue BO in EMT6-S and EMT6-R cells using confocal microscopy.

机构信息

Department of Forensic Science, University of Central Lancashire, Preston, PR1 2HE, UK.

出版信息

Cytotechnology. 2002 May;39(1):15-25. doi: 10.1023/A:1022435829894.

DOI:10.1023/A:1022435829894
PMID:19003300
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3449804/
Abstract

The subcellular localisation of doxorubicin and Victoria Blue BO (VBBO) in a murine mammary tumour cell line EMT6-S, and the resistant sub-lineEMT6-R was studied, using confocal microscopy, in order to investigate their sites of action. In cells treated with doxorubicin (10 mu M) for 90 min, the pattern of intracellular drug distribution differed between the two cell lines. Doxorubicin was found to localise mainly in the nucleus of the sensitive cell line, whereas weak fluorescence was observed in the cytoplasm of the resistant cells, in a punctuate pattern, with no nuclear involvement. The drug also appeared to be effluxed more rapidly by the resistant cell line. The accumulation of doxorubicin at various time intervals over 1h in EMT6-S cells showed that the drug clearly interacted with both the plasma membrane and the nucleus. In contrast to doxorubicin, the intracellular distribution of VBBO in both EMT6-S and EMT6-R was similar, VBBO was clearly localised throughout the cytoplasm, in a punctuate pattern, which may be consistent with the widespread distribution of mitochondria. A more apical pattern of accumulation was noted in the EMT6-R cell line. No interaction with the plasma membrane was evident. These results indicate that the main modes of action for the two drugs differ markedly, suggesting involvement of both the membrane and the nucleus in the case of doxorubicin, but mitochondrial involvement for VBBO.

摘要

使用共聚焦显微镜,研究了阿霉素(10 μM)作用 90 分钟后,在鼠乳腺肿瘤细胞系 EMT6-S 和耐药细胞系 EMT6-R 中的亚细胞定位,以研究它们的作用部位。在两种细胞系中,阿霉素的细胞内分布模式不同。阿霉素主要定位于敏感细胞系的细胞核中,而耐药细胞的细胞质中则呈现点状弱荧光,没有核参与。耐药细胞系似乎更快地将药物排出。在 EMT6-S 细胞中,1 小时内不同时间点阿霉素的积累表明,该药物显然与质膜和核相互作用。与阿霉素不同,VBBO 在 EMT6-S 和 EMT6-R 中的细胞内分布相似,VBBO 明显定位于整个细胞质中,呈点状,这可能与线粒体的广泛分布一致。在 EMT6-R 细胞系中,注意到积累的更顶模式。没有证据表明与质膜相互作用。这些结果表明,两种药物的主要作用模式明显不同,表明阿霉素的作用涉及膜和核,而 VBBO 的作用涉及线粒体。