Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/9706
Title: Anti-proliferative and anti-invasive effects of ferulic acid in TT medullary thyroid cancer cells interacting with URG4/URGCP
Authors: Dodurga, Yavuz
Eroğlu, C.
Seçme, Mücahit
Elmas, Levent
Avcı, Ç.B.
Şatıroğlu-Tufan, Naciye Lale
Keywords: Ferulic acid
Thyroid cancer
TT cells
URG4/URGCP
CASP3 protein
CASP9 protein
cyclin dependent kinase 4
cyclin dependent kinase 6
ferulic acid
gelatinase A
gelatinase B
messenger RNA
nicotinamide adenine dinucleotide adenosine diphosphate ribosyltransferase 1
phenol derivative
protein
protein Bax
protein bcl 2
protein Bid
protein Noxa
protein p53
PUMA protein
TIMP1 protein
unclassified drug
coumaric acid
tumor protein
URG4 protein, human
antiinvasive activity
antiproliferative activity
apoptosis
Article
BAX gene
BCL2 gene
BID gene
CASP3 gene
CASP9 gene
CCND1 gene
CDK4 gene
CDK6 gene
cell cycle
cell cycle arrest
cell invasion
cell migration
cell viability
colony formation
controlled study
drug activity
gene
gene expression
human
human cell
IC50
medullary thyroid carcinoma cell
MMP2 gene
MMP9 gene
NOXA gene
p53 gene
PARP gene
priority journal
PUMA gene
real time polymerase chain reaction
thyroid medullary carcinoma
TIMP1 gene
upregulation
URG4 gene
URGCP gene
wound healing
Carcinoma, Neuroendocrine
cell cycle checkpoint
cell motion
cell proliferation
cell survival
drug effects
gene expression regulation
metabolism
signal transduction
Thyroid Neoplasms
tumor cell line
Apoptosis
Cell Cycle Checkpoints
Cell Line, Tumor
Cell Movement
Cell Proliferation
Cell Survival
Coumaric Acids
Gene Expression Regulation, Neoplastic
Humans
Neoplasm Proteins
RNA, Messenger
Signal Transduction
Up-Regulation
Publisher: Springer Netherlands
Abstract: Ferulic acid (4-hydroxy-3-methoxycinnamic acid; FA), a common dietary plant phenolic compound, is abundant in fruits and vegetables. The aim of present study is to investigate the effects of FA on cell cycle, apoptosis, invasion, migration, and colony formation in the TT medullary thyroid cancer cell line. The effect of FA on cell viability was determined by using CellTiter-Glo assay. IC50 dose in the TT cells was detected as 150 µM. URG4/URGCP (upregulated gene-4/upregulator of cell proliferation) is a novel gene in full-length mRNA of 3.607 kb located on 7p13. It was determined that FA caused a decrease in the expression of novel gene URG4/URGCP, CCND1, CDK4, CDK6, BCL2, MMP2, and MMP9, a significant increase in the expression of p53, PARP, PUMA, NOXA, BAX, BID, CASP3, CASP9, and TIMP1 genes in TT human thyroid cancer cell line by using real-time PCR. It was found that FA in TT cells suppressed invasion, migration, and colony formation by using matrigel invasion chamber, wound healing, and colony formation assay, respectively. In conclusion, it is thought that FA indicates anticarcinogenesis activity by affecting cell cycle arrest, apoptosis, invasion, migration, and colony formation on TT cells. © 2015, International Society of Oncology and BioMarkers (ISOBM).
URI: https://hdl.handle.net/11499/9706
https://doi.org/10.1007/s13277-015-3984-z
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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