Effects of Kinetin Riboside on Proliferation and Proapoptotic Activities in Human Normal and Cancer Cell Lines

被引:22
作者
Dudzik, Paulina [1 ]
Dulinska-Litewka, Joanna [1 ]
Wyszko, Eliza [2 ]
Jedrychowska, Patrycja [3 ]
Opalka, Maciej [1 ]
Barciszewski, Jan [2 ]
Laidler, Piotr [1 ]
机构
[1] Jagiellonian Univ, Chair Med Biochem, Coll Med, PL-31034 Krakow, Poland
[2] Polish Acad Sci, Inst Bioorgan Chem, Poznan, Poland
[3] Jagiellonian Univ, Dept Conservat Dent Endodont, Coll Med, PL-31034 Krakow, Poland
关键词
KINETIN RIBOSIDE; CASPASE-3; APOPTOSIS; CANCER; PROSTATE; BREAST; MELANOMA; BCL-2; FAMILY-MEMBERS; CASPASE ACTIVATION; APOPTOSIS; MITOCHONDRIA; PATHWAYS; DEATH; IDENTIFICATION; CHEMOTHERAPY; INHIBITION; PROTEINS;
D O I
10.1002/jcb.23132
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
Kinetin riboside (KR) is a N6-substituted derivative of adenosine. It is a natural compound which occurs in the milk of coconuts on the nanomole level. KR was initially shown to selectively inhibit proliferation of cancer cells and induce their apoptosis. We observed that KR inhibited growth (20-80%) of not only human cancer, but also normal cells and that this effect strongly depended on the type of cells. The anti-apoptotic Bcl-2 protein was downregulated, while proapoptotic Bax was upregulated in normal as well as in cancer cell lines, upon exposure to KR. Cytochrome c level increased in the cytosol upon treatment of cells with KR. The activity of caspases (ApoFluor (R) Green Caspase Activity Assay), as well as caspase-3 (caspase-3 activation assay) were increased mainly in cancer cells. The expression of procaspase 9 and its active form in the nucleus as well as in cytosol of KR-treated cells was elevated. In contrast, no effect of KR on caspase 8 expression was noted. The results indicated that non-malignant cells were less sensitive to KR then their cancer analogs and that KR most likely stimulated apoptosis mechanism of cancer cells through the intrinsic pathway. J. Cell. Biochem. 112: 2115-2124, 2011. (C) 2011 Wiley-Liss, Inc.
引用
收藏
页码:2115 / 2124
页数:10
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