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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 |
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