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   <subfield code="a">10.1007/s10620-011-1774-z</subfield>
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   <subfield code="a">Aberrant Methylation of Different DNA Repair Genes Demonstrates Distinct Prognostic Value for Esophageal Cancer</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Zhi-Qiang Ling, Pei Li, Ming-Hua Ge, Fu-Jun Hu, Xian-Hua Fang, Zi-Min Dong, Wei-Min Mao]</subfield>
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   <subfield code="a">Background: DNA mismatch repair (MMR) deficiency results in a strong mutator phenotype and high-frequency microsatellite instability (MSI-H), which are the hallmarks of many tumors. Aim: The objective of this study is to investigate the promoter CpG island methylation status of mismatch repair genes human mutL homolog 1 (hMLH1), human mutS homolog 2 (hMSH2), and O6-methylguanine-DNA methyltransferase (MGMT) in esophageal squamous cell carcinoma (ESCC) and its roles in alkylating agents chemotherapy. Methods: Real-time methylation-specific polymerase chain reaction (PCR) (real-time MSP) was employed to detect promoter CpG island methylation of the hMLH1, hMSH2, as well as MGMT genes in 235 surgical tumor tissue samples from ESCC patients and their corresponding normal tissue samples. Results: Promoter CpG island methylation of hMLH1, hMSH2, and MGMT were detectable in 43.4, 28.9, and 40.4% of ESCC tumor DNA, respectively, and the loss rates of hMLH1, hMSH2, and MGMT protein expression were 48.6, 34.5, and 40.9% in tumor tissues, respectively. For the entire population of 235 ESCC patients who were enrolled in operating treatment combined with radiotherapy and chemotherapy with alkylating agents, there was a significant difference in the overall survival between patients with methylated MGMT promoter and those with an unmethylated MGMT promoter (P&lt;0.05). Conclusion: Promoter CpG island methylation may be a frequent event in ESCC carcinogenesis. Detection of the methylated sequences of hMLH1, hMSH2, and MGMT appears to be promising as a predictive factor in primary ESCC.</subfield>
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   <subfield code="a">Springer Science+Business Media, LLC, 2011</subfield>
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   <subfield code="a">Esophageal squamous cell carcinoma (ESCC)</subfield>
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   <subfield code="a">Promoter CpG island hypermethylation</subfield>
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   <subfield code="a">O6-methylguanine-DNA methyltransferase ( MGMT ) gene</subfield>
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   <subfield code="a">Human mutL homolog 1 ( hMLH1 ) gene</subfield>
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   <subfield code="a">Human mutS homolog 2 ( hMSH2 ) gene</subfield>
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   <subfield code="a">Prognosis</subfield>
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   <subfield code="a">Ling</subfield>
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   <subfield code="u">Zhejiang Cancer Research Institute, Zhejiang Province Cancer Hospital, Zhejiang Cancer Center, No. 38 Guangji Rd., Banshanqiao District, 310022, Hangzhou, People's Republic of China</subfield>
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   <subfield code="a">Li</subfield>
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   <subfield code="u">Department of Pathophysiology, College of Medical Sciences, Zhengzhou University, 450052, Zhengzhou, People's Republic of China</subfield>
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   <subfield code="u">Department of Tumor Surgery, Zhejiang Province Cancer Hospital, Zhejiang Cancer Center, No. 38 Guangji Rd., Banshanqiao District, 310022, Hangzhou, People's Republic of China</subfield>
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   <subfield code="u">Department of Radiotherapy, Zhejiang Province Cancer Hospital, Zhejiang Cancer Center, No. 38 Guangji Rd., Banshanqiao District, 310022, Hangzhou, People's Republic of China</subfield>
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   <subfield code="t">Digestive Diseases and Sciences</subfield>
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