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https://hdl.handle.net/11499/9974
Title: | Assessment of the anticancer mechanism of ferulic acid via cell cycle and apoptotic pathways in human prostate cancer cell lines | Authors: | Eroğlu, C. Seçme, Mücahit. Bağcı, Gülseren. Dodurga, Yavuz |
Keywords: | Apoptosis Cell cycle Colony formation Ferulic acid Invasion Prostate cancer beta arrestin 1 CASP1 gene CASP2 gene CASP8 gene CYCS gene deoxyuridine triphosphate derivative FAS gene FASLG gene ferulic acid protein bcl 2 protein p53 RNA TRADD gene transcription factor E2F4 unclassified drug X linked inhibitor of apoptosis coumaric acid tumor protein antineoplastic activity apoptosis Article cancer cell CCND1 gene CCND2 gene CCND3 gene CDK2 gene CDK4 gene CDK6 gene CDKN1A gene CDKN1B gene cell cycle cell cycle arrest cell invasion cell proliferation cell viability colony formation drug mechanism gene gene expression heredity human IC50 male priority journal prostate cancer protein expression reverse transcription polymerase chain reaction TUNEL assay Western blotting biosynthesis cell cycle checkpoint cell survival drug effects gene expression regulation genetics pathology Prostatic Neoplasms signal transduction tumor cell line tumor invasion Cell Cycle Checkpoints Cell Line, Tumor Cell Proliferation Cell Survival Coumaric Acids Gene Expression Regulation, Neoplastic Humans Male Neoplasm Invasiveness Neoplasm Proteins Signal Transduction |
Publisher: | Springer Netherlands | Abstract: | Studies on genetic changes underlying prostate cancer and the possible signaling pathways are getting increased day by day, and new treatment methods are being searched for. The aim of the present study is to investigate the effects of ferulic acid (FA), a phenolic compound, on cell cycle, apoptosis, invasion, and colony formation in the PC-3 and LNCaP prostate cancer cells. The effect of FA on cell viability was determined via a 2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT) method. Total RNA was isolated with Tri Reagent. Expression of 84 genes for both cell cycle and apoptosis separately was evaluated by reverse transcriptase PCR (RT-PCR). Protein expressions were evaluated by Western blot analysis. Furthermore, apoptotic effects of FA were observed with terminal deoxynucleotidyl transferase deoxyuridine triphosphate nick end labeling (TUNEL) assay. Effects of FA on cell invasion and colony formation were determined using Matrigel chamber and colony assay, respectively. The half maximal inhibitory concentration (IC50) dose of FA was found to be 300 µM in PC-3 cells and 500 µM in LNCaP cells. According to RT-PCR results, it was observed that FA inhibited cell proliferation by increasing the gene expressions of ATR, ATM, CDKN1A, CDKN1B, E2F4, RB1, and TP53 and decreasing the gene expressions of CCND1, CCND2, CCND3, CDK2, CDK4, and CDK6 in PC-3 cells. On the other hand, it was seen that FA suppressed cell proliferation by increasing in the gene expressions of CASP1, CASP2, CASP8, CYCS, FAS, FASLG, and TRADD and decreasing in the gene expressions of BCL2 and XIAP in LNCaP cells. In this study, protein expression of CDK4 and BCL2 genes significantly decreased in these cells. It could induce apoptosis in PC-3 and LNCaP cells. Also, it was observed that FA suppressed the invasion in PC-3 and LNCaP cells. Moreover, it suppressed the colony formation. In conclusion, it has been observed that FA may lead to cell cycle arrest in PC-3 cells while it may cause apoptosis in LNCaP cells. © 2015, International Society of Oncology and BioMarkers (ISOBM). | URI: | https://hdl.handle.net/11499/9974 https://doi.org/10.1007/s13277-015-3689-3 |
ISSN: | 1010-4283 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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