Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/8646
Title: Detection of deleted in malignant brain tumors 1 and runt-related transcription factor 3 gene expressions in bladder carcinoma
Authors: Dodurga, Yavuz
Avci, C.B.
Satıroğlu-Tufan, Naciye lale
Tataroglu, C.
Kesen, Z.
Dogan, Z.O.
Yilmaz, S.
Keywords: Bladder cancer
DMBT1
Paraffin tissue
RUNX3
complementary DNA
messenger RNA
paraffin
transcription factor RUNX3
cell surface receptor
DMBT1 protein, human
Runx3 protein, human
aged
article
bladder carcinogenesis
bladder carcinoma
cancer grading
cancer localization
cancer prognosis
clinical feature
deleted in malignant brain tumors 1 gene
disease association
DNA sequence
DNA synthesis
down regulation
female
gene expression profiling
gene identification
genetic association
human
human tissue
male
molecular pathology
nucleotide sequence
oncogene
reverse transcription polymerase chain reaction
RNA extraction
runt related transcription factor 3 gene
transitional cell carcinoma
bladder tumor
gene expression regulation
genetics
metabolism
middle aged
pathology
Aged
Core Binding Factor Alpha 3 Subunit
Female
Gene Expression Regulation, Neoplastic
Humans
Male
Middle Aged
Neoplasm Grading
Receptors, Cell Surface
Urinary Bladder Neoplasms
Abstract: Bladder cancer is the fifth most commonly diagnosed cancer in the United States, where the majority of tumors are transitional cell carcinoma. Deleted in malignant brain tumors 1 (DMBT1) gene is located at chromosome 10q25.3-q26.1. DMBT1 gene expression has yet to be investigated in patients with bladder cancer. Runtrelated transcription factor 3 (RUNX3) is a candidate tumor suppressor gene which is localized on the chromosome 1p36. RUNX3 gene expression in bladder carcinogenesis is particularly unknown. We aimed to evaluate DMBT1 and RUNX3 gene expression profiles in bladder cancer and how their expressions could be related to carcinogenesis in the bladder and their correlation with clinicopathological parameters. Fifty-six paraffin embedded specimens of transitional cell carcinoma of the urinary bladder were used. Total RNA was extracted from bladder specimens and cDNA was synthesized. The quantification of DMBT1 and RUNX3 mRNAs were succeeded according to the manufacturers' instructions by using RT-PCR. DMBT1 and RUNX3 gene expressions were identified in 100% of bladder carcinoma samples. No significant association was found in these genes expression levels when compared to sex and age. RUNX3 gene expression was decreased nonsignificantly in high-grade tumors. When DMBT1 gene expression was compared to tumor grades, a significant decrease was detected between grade I and III (P = 0.028). Disruption of expression in relation to tumor suppressors like DMBT1 and RUNX3 genes was associated with bladder cancer. Furthermore, detailed studies including these genes should be performed in protein levels and used more patient specimens in a large scale study. © Springer Science+Business Media B.V. 2011.
URI: https://hdl.handle.net/11499/8646
https://doi.org/10.1007/s11033-011-1261-9
ISSN: 0301-4851
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

Show full item record



CORE Recommender

SCOPUSTM   
Citations

6
checked on Dec 14, 2024

WEB OF SCIENCETM
Citations

4
checked on Dec 20, 2024

Page view(s)

60
checked on Aug 24, 2024

Google ScholarTM

Check




Altmetric


Items in GCRIS Repository are protected by copyright, with all rights reserved, unless otherwise indicated.