Changes in expression of genes encoding antioxidant enzymes, heme oxygenase-1, Bcl-2, and Bcl-xl and in level of reactive oxygen species in tumor cells resistant to doxorubicin

被引:21
作者
Kalinina, E. V.
Chernov, N. N.
Saprin, A. N.
Kotova, Ya. N.
Andreev, Ya. A.
Solomka, V. S.
Scherbak, N. P.
机构
[1] Russian Acad Sci, Ctr Theoret Problems Physicochem Pharmacol, Moscow 119991, Russia
[2] Inst Cytochem & Mol Pharmacol, Moscow 115404, Russia
[3] Patrice Lumumba Peoples Friendship Univ, Moscow 117198, Russia
[4] Russian Acad Sci, Shemyakin & Ovchinnikov Inst Bioorgan Chem, Moscow 117997, Russia
[5] Russian Acad Med Sci, Inst Carcinogenesis, Blokhin Russian Canc Res Ctr, Moscow 115478, Russia
关键词
drug resistance of cancer cells; doxorubicin; reactive oxygen species; antioxidant enzymes; heme oxygenase-1; Bcl-2; Bcl-xl;
D O I
10.1134/S0006297906110058
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The relationship between expression of genes encoding key antioxidant enzymes, heme oxygenase-1, Bcl-2, and Bcl-xl and change in production of reactive oxygen species (ROS) resulting from development of resistance of cancer cells K562, MCF-7, and SKOV-3 to the prooxidant chemotherapeutic agent doxorubicin (DOX) has been studied. Significant increase in mRNA level and activity of Mn-superoxide dismutase (Mn-SOD), catalase, and selenium-dependent glutathione peroxidase-1 (GPx-1) and reduced ROS level was found in resistant K562/DOX and SKVLB cells. In contrast, no change in ROS level was observed in MCF-7/DOX cells in parallel with decrease in Mn-SOD and catalase mRNAs and corresponding activities concurrently with high increase in GPx-1 mRNA and activity. As a result of the development of resistance, a similarity was found between the change in ROS level and the change in ho-1 and bcl-2 gene expression, whereas elevation of bcl-xl gene expression was observed in all three types of resistant cells. Particular features of development of adaptive antioxidant response as well as redox-dependent change in bcl-2 gene expression under formation of DOX resistance of cancer cells of different genesis are discussed.
引用
收藏
页码:1200 / 1206
页数:7
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