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   <subfield code="a">10.1245/s10434-010-1271-1</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1245/s10434-010-1271-1</subfield>
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   <subfield code="a">STC2: A Predictive Marker for Lymph Node Metastasis in Esophageal Squamous-Cell Carcinoma</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Yoshiaki Kita, Koshi Mimori, Masaaki Iwatsuki, Takehiko Yokobori, Keisuke Ieta, Fumiaki Tanaka, Hideshi Ishii, Hiroshi Okumura, Shoji Natsugoe, Masaki Mori]</subfield>
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   <subfield code="a">Background: We sought to identify genes associated with the progression and metastasis of esophageal squamous-cell cancer by comparing the expression profiles of normal, primary cancer, and metastatic cancer cells isolated with laser microdissection. Methods: Oligo microarray analysis identified several lymph node-specific, metastasis-related genes. STC2 (stanniocalcin 2), which was overexpressed in esophageal cancer cases, was chosen for further characterization. Quantitative reverse transcriptase-polymerase chain reaction and immunohistochemistry were used to explore the clinicopathologic significance of STC2 expression status in 70 cases. Additionally, the functional role of STC2 in esophageal cancer was studied by the attenuation of STC2 in an esophageal cancer cell line. Results: Laser microdissection and oligo microarray analysis identified 63 candidate genes. Among them, STC2 showed higher expression in cancer tissue than in corresponding normal tissue (P &lt; 0.001). STC2 expression was significantly correlated with lymph node metastasis, lymphatic invasion, and distant metastasis (P=0.005, 0.007, and 0.038, respectively). Patients whose tumors had high STC2 expression had a worse 5-year survival rate than patients whose tumors had a low STC2 expression level (P=0.016). STC2 transfected cells had a significantly higher proliferation rate than control cells (P &lt; 0.001). Additionally, STC2 transfected cells were more invasive in vitro (P &lt; 0.001) than control cells. These findings were validated by means of RNA interference assays. Conclusions: We identified lymph node-specific, metastasis-related genes in esophageal cancer cells. One of these, STC2, may be associated with lymph node metastasis, making it a potential prognostic marker for esophageal cancer patients.</subfield>
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   <subfield code="a">Kita</subfield>
   <subfield code="D">Yoshiaki</subfield>
   <subfield code="u">Department of Surgery, Medical Institute of Bioregulation, Kyushu University, Beppu, Japan</subfield>
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   <subfield code="a">Mimori</subfield>
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   <subfield code="u">Department of Surgery, Medical Institute of Bioregulation, Kyushu University, Beppu, Japan</subfield>
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   <subfield code="a">Iwatsuki</subfield>
   <subfield code="D">Masaaki</subfield>
   <subfield code="u">Department of Surgery, Medical Institute of Bioregulation, Kyushu University, Beppu, Japan</subfield>
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   <subfield code="a">Yokobori</subfield>
   <subfield code="D">Takehiko</subfield>
   <subfield code="u">Department of Surgery, Medical Institute of Bioregulation, Kyushu University, Beppu, Japan</subfield>
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   <subfield code="u">Department of Surgery, Medical Institute of Bioregulation, Kyushu University, Beppu, Japan</subfield>
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   <subfield code="a">Tanaka</subfield>
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   <subfield code="u">Department of Surgery, Medical Institute of Bioregulation, Kyushu University, Beppu, Japan</subfield>
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   <subfield code="u">Department of Surgery, Medical Institute of Bioregulation, Kyushu University, Beppu, Japan</subfield>
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   <subfield code="a">Natsugoe</subfield>
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   <subfield code="u">Department of Surgical Oncology and Digestive Surgery, Field of Oncology, Course of Advanced Therapeutics, Kagoshima University Graduate School of Medical and Dental Science, Kagoshima, Japan</subfield>
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   <subfield code="u">Department of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Suita, Japan</subfield>
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   <subfield code="t">Annals of Surgical Oncology</subfield>
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