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Expression Patterns of Cxcl12 and Its Receptor in Colorectal Carcinoma Publisher Pubmed



Mousavi A1 ; Hashemzadeh S2 ; Bahrami T3 ; Estiar MA3 ; Feizi MAH4 ; Pouladi N5 ; Rostamizadeh L1 ; Sakhinia E1, 6
Authors
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Authors Affiliations
  1. 1. Department of Biochemistry and Clinical Laboratories, Division of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
  2. 2. Liver and Gastrointestinal Disease Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
  3. 3. Department of Medical Genetics, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Animal Biology, Faculty of Natural Science, Tabriz University, Tabriz, Iran
  5. 5. Department of Biology, Faculty of Science, Azarbaijan Shahid Madani University, Tabriz, Iran
  6. 6. Connective Tissue Disease Research Center, Tabriz University of Medical Sciences, Tabriz, Iran

Source: Clinical Laboratory Published:2018


Abstract

Background: Stromal cell-derived factor-1 (also called CXCL12) and its receptor, CXCR4, have a key role in the pathogenesis and tumorigenesis of various cancers. The aims of the current study were to quantitatively examine the expression of CXCR4 and CXCL12 genes in colorectal cancer and to correlate their expression degree with clinicopathological features. Methods: Tumor tissue samples were collected from 47 patients with CRC. Total RNA was isolated from resection tissues and real-time PCR analysis was performed to examine mRNA levels of CXCL12 and CXCR4 genes. Results: No significant differences were observed for both CXCL12 and CXCR4 between tumor tissues and the adjacent non-affected tissues, although a borderline significant correlation (p = 0.052) were detected between gene expression of CXCL12 and CXCR4 in tumor tissues. Our results also indicated that there was no significant correlation between expression pattern of CXCL12/CXCR4 and clinicopathological variables. Conclusions: Our data showed that CXCL12 and CXCR4 are expressed simultaneously in colorectal carcinoma tissues, suggesting that expression of these chemokines and corresponding receptors may play a pivotal role in colorectal tumorigenesis, although it cannot be as a predictive factor for disease progression. © 2018 Verlag Klinisches Labor GmbH. All rights reserved.