2012
DOI: 10.1016/j.fct.2012.08.031
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Mechanisms of natural brassinosteroid-induced apoptosis of prostate cancer cells

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Cited by 45 publications
(46 citation statements)
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“…BS treatment resulted in arrest of cell cycle in the G1 phase and an induction of apoptosis [104,110]. A range of techniques including flow cytometry, Western blotting, TUNEL, DNA ladder assays and immunofluorescence analyses was used for study of BS-induced apoptosis of human prostate cancer cell lines LNCaP and DU-145 [111]. Cell growth inhibition and G 1 cell cycle arrest were accompanied by reductions in cyclin D1, CDK4/6 and pRb expression.…”
Section: Anticancer Effectsmentioning
confidence: 99%
“…BS treatment resulted in arrest of cell cycle in the G1 phase and an induction of apoptosis [104,110]. A range of techniques including flow cytometry, Western blotting, TUNEL, DNA ladder assays and immunofluorescence analyses was used for study of BS-induced apoptosis of human prostate cancer cell lines LNCaP and DU-145 [111]. Cell growth inhibition and G 1 cell cycle arrest were accompanied by reductions in cyclin D1, CDK4/6 and pRb expression.…”
Section: Anticancer Effectsmentioning
confidence: 99%
“…On the other hand, a growing body of data suggests that brassinosteroids might be the putative inducers of the activity of the glucocorticoid receptor. These considerations are based on the effects of brassinosteroids in human systems Steigerová et al 2012), and the resemblance of plant steroid signalling processes to those of ecdysteroids in Drosophila (Thummel and Chory 2002), both sharing a range of common developmental and physiological responses to stress. To support this idea, there is a large body of evidence for the anti-stress behaviour of brassinosteroids (Dhaubhadel et al 2002;Choudhary et al 2012;Kanwar et al 2012;Li et al 2012).…”
Section: Discussionmentioning
confidence: 99%
“…Rárová et al (2012) showed that brassinosteroids inhibit angiogenesis in human endothelial cells and interact with human steroid receptors such as the oestrogen receptors a and b and the androgen receptor. Moreover, Steigerová et al (2012) found that brassinosteroids mediated the apoptosis of human cancer cells by inducing cellular block and stopping cells at the G1 stage. The glucocorticoid receptor (GR) is a mammalian nuclear hormone-receptor transcription factor (Giguere et al 1986) that is activated by glucocorticoids, a class of steroid hormones, synthesized in the adrenal cortex, and popular as anti-inflammatory and immunosuppressive therapeutic agents (Mangelsdorf et al 1995).…”
Section: Introductionmentioning
confidence: 99%
“…The mechanism of antiproliferative activity of 28-homoCS and 24-EpiBL was studied by Steigerova et al [51,65] in prostate cancer cell lines, DU-145 and LNCaP (hormone insensitive and sensitive). Various techniques like flow cytometry, TUNEL DNA ladder Test, Western blotting, and immunofluorescence were used to study the effect of these BRs on prostate cancer cells.…”
Section: Anticancerous/antiproliferative Activitiesmentioning
confidence: 99%