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DLC-1 is a candidate biomarker methylated and down-regulated in pancreatic ductal adenocarcinoma

Pancreatic ductal adenocarcinoma (PDA) is one of the most aggressive malignancies in humans, and its prognosis is generally poor even after surgery. Many advances have been made to understand the pathogenesis of PDA; however, the molecular mechanisms that lead to pancreatic carcinogenesis are still...

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Published in:Tumor biology 2013-10, Vol.34 (5), p.2857-2861
Main Authors: Xue, Yu-Zheng, Wu, Tie-Long, Wu, Yan-Min, Sheng, Ying-Yue, Wei, Zhe-Qiang, Lu, Yu-Feng, Yu, Li-Hua, Li, Jian-Ping, Li, Zhao-Shen
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Language:English
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Summary:Pancreatic ductal adenocarcinoma (PDA) is one of the most aggressive malignancies in humans, and its prognosis is generally poor even after surgery. Many advances have been made to understand the pathogenesis of PDA; however, the molecular mechanisms that lead to pancreatic carcinogenesis are still not clearly understood. The aims of this study were to investigate the relationship between DLC-1 methylation status and clinicopathological characteristics of PDA patients and evaluate the role of DLC-1 methylation status in PDA. The expression of DLC-1 mRNA in PDA tissues was analyzed by real-time PCR. The methylation status of DLC-1 was analyzed by methylation-specific polymerase chain reaction (MSP). Furthermore, we determined the prognostic importance of DLC-1 methylation status in PDA patients. Our results showed that the expression level of DLC-1 mRNA in PDA tissues was lower than that in non-cancerous tissues. The rate of DLC-1 promoter methylation was significantly higher in PDA tissues than in adjacent non-cancerous tissues ( p  
ISSN:1010-4283
1423-0380
DOI:10.1007/s13277-013-0846-4