Please use this identifier to cite or link to this item: 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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