Anticancer mechanism of Sinapic acid in PC-3 and LNCaP human prostate cancer cell lines

Sinapic acid (SA) is a derivative of hydroxycinnamic acid and found in various vegetables and fruit species. Aim was to evaluate the anticancer effects of SA in PC-3 and LNCaP human prostate cancer cells. The effect of SA on cell viability was determined using XTT assay. Expressions of 8 genes for a...

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Bibliographic Details
Published inGene Vol. 671; pp. 127 - 134
Main Authors Eroğlu, Canan, Avcı, Ebru, Vural, Hasibe, Kurar, Ercan
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 10.09.2018
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Summary:Sinapic acid (SA) is a derivative of hydroxycinnamic acid and found in various vegetables and fruit species. Aim was to evaluate the anticancer effects of SA in PC-3 and LNCaP human prostate cancer cells. The effect of SA on cell viability was determined using XTT assay. Expressions of 8 genes for apoptosis and 6 genes for metastasis were evaluated by qPCR. Caspase-3 activity was determined using caspase-3 colorimetric assay kit. Effect of SA on cell invasion was evaluated with cell invasion assay. The IC50 dose of SA in PC-3 and LNCaP cells was found to be 1000 μM for 72 h. SA treatment increased the expression of BAX, CASP3, CASP8, CYCS, FAS, TIMP-1 and CDH1 however significantly decreased the expression of MMP-9 in PC-3 cells. In LNCaP cells, the expressions of BAX, CASP3, CASP7 and CYCS were significantly elevated; however, a decrease was seen in the expressions of CDH2, MMP-2 and MMP-9 in the SA treatment. Moreover, SA significantly increased caspase-3 activity and suppressed the cell invasion. In conclusion, it is thought that SA has anticancer effect on prostate cancer cells. However, more detailed studies should be conduct to illuminate molecular mechanism of apoptotic and antimetastatic activity of SA. •SA showed cytotoxic effect in PC-3 and LNCaP human prostate cancer cells.•SA induced apoptosis and caspase-3 activity in human prostate cancer cells.•SA suppressed the cell invasion in human prostate cancer cells.
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ISSN:0378-1119
1879-0038
DOI:10.1016/j.gene.2018.05.049