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   <subfield code="a">10.1245/s10434-011-1636-0</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1245/s10434-011-1636-0</subfield>
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   <subfield code="a">Aberrant Gene Methylation Is a Biomarker for the Detection of Cancer Cells in Peritoneal Wash Samples from Advanced Gastric Cancer Patients</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Masatsugu Hiraki, Yoshihiko Kitajima, Yasuo Koga, Tomokazu Tanaka, Jun Nakamura, Kazuyoshi Hashiguchi, Hirokazu Noshiro, Kohji Miyazaki]</subfield>
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   <subfield code="a">Purpose: To assess whether gene methylation in peritoneal fluid (PF) is clinically feasible for determining micrometastasis to the peritoneum in gastric cancer. Methods: The gene methylation of BNIP3, CHFR, CYP1B1, MINT25, SFRP2, and RASSF2 were analyzed in 107 specimens of PF by quantitative methylation-specific polymerase chain reaction. All patients were placed into one of 3 groups: group A (n=42), patients with depth of cancer invasion at muscularis propria (MP) or less than MP; group B (n=45), depth of cancer invasion beyond the MP; and group C (n=20), histologically diagnosed peritoneal metastasis or cancer cells cytologically defined in the peritoneal cavity. Patients in both groups A and B were diagnosed as having no cancer cells by peritoneal cytology and histology. Results: The methylation status of the 6 genes was found to be significantly different among the 3 groups (group A, 0-5%; group B, 0-15%; group C, 15-45%; P&lt;0.01). Furthermore, the rate of positive methylation in any of the 6 genes was significantly different in each group (group A, 7%; group B, 20%; group C, 75%; P&lt;0.001). Three of 9 patients in group B with positive methylation in any of 6 genes experienced peritoneal recurrence. On the other hand, only 1 of 36 patients without gene methylation experienced peritoneal recurrence (P&lt;0.05). Conclusions: DNA methylation in PFs is a possible marker detecting occult neoplastic cells on the peritoneum. Methylation analysis along with a cytological examination might therefore improve the positive detection of cancer cells in PF of gastric cancer.</subfield>
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   <subfield code="a">Society of Surgical Oncology, 2011</subfield>
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   <subfield code="a">Hiraki</subfield>
   <subfield code="D">Masatsugu</subfield>
   <subfield code="u">Department of Surgery, Saga University Faculty of Medicine, Saga, Japan</subfield>
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   <subfield code="a">Kitajima</subfield>
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   <subfield code="a">Koga</subfield>
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   <subfield code="a">Tanaka</subfield>
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   <subfield code="u">Department of Surgery, Saga University Faculty of Medicine, Saga, Japan</subfield>
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   <subfield code="a">Nakamura</subfield>
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   <subfield code="u">Department of Surgery, Saga University Faculty of Medicine, Saga, Japan</subfield>
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   <subfield code="a">Hashiguchi</subfield>
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   <subfield code="u">Department of Surgery, Saga University Faculty of Medicine, Saga, Japan</subfield>
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   <subfield code="u">Department of Surgery, Saga University Faculty of Medicine, Saga, Japan</subfield>
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   <subfield code="a">Miyazaki</subfield>
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   <subfield code="u">Department of Surgery, Saga University Faculty of Medicine, Saga, Japan</subfield>
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   <subfield code="t">Annals of Surgical Oncology</subfield>
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   <subfield code="g">18/10(2011-10-01), 3013-3019</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
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