c-MYC Amplification in Mucinous Gastric Carcinoma: A Possible Genetic Alteration Leading to Deeply Invasive Tumors
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作者:
Choi, Jong-Sun
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Dongguk Univ, Dept Pathol, Ilsan Hosp, Goyang, South KoreaSeoul Natl Univ, Coll Med, Dept Pathol, Seoul 110799, South Korea
Choi, Jong-Sun
[2
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Seo, Jinwon
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Hallym Univ, Sacred Heart Hosp, Coll Med, Dept Pathol, Anyang, South KoreaSeoul Natl Univ, Coll Med, Dept Pathol, Seoul 110799, South Korea
Seo, Jinwon
[3
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Jung, Eun Ji
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Seoul Natl Univ, Coll Med, Canc Res Inst, Seoul 110799, South KoreaSeoul Natl Univ, Coll Med, Dept Pathol, Seoul 110799, South Korea
Jung, Eun Ji
[4
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Kim, Eo Jin
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Dongguk Univ, Dept Pathol, Ilsan Hosp, Goyang, South KoreaSeoul Natl Univ, Coll Med, Dept Pathol, Seoul 110799, South Korea
Kim, Eo Jin
[2
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Lee, Geon Kook
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Natl Canc Ctr, Dept Pathol, Goyang, South KoreaSeoul Natl Univ, Coll Med, Dept Pathol, Seoul 110799, South Korea
Lee, Geon Kook
[5
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Kim, Woo Ho
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Seoul Natl Univ, Coll Med, Dept Pathol, Seoul 110799, South Korea
Seoul Natl Univ, Coll Med, Canc Res Inst, Seoul 110799, South KoreaSeoul Natl Univ, Coll Med, Dept Pathol, Seoul 110799, South Korea
Kim, Woo Ho
[1
,4
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机构:
[1] Seoul Natl Univ, Coll Med, Dept Pathol, Seoul 110799, South Korea
[2] Dongguk Univ, Dept Pathol, Ilsan Hosp, Goyang, South Korea
[3] Hallym Univ, Sacred Heart Hosp, Coll Med, Dept Pathol, Anyang, South Korea
[4] Seoul Natl Univ, Coll Med, Canc Res Inst, Seoul 110799, South Korea
[5] Natl Canc Ctr, Dept Pathol, Goyang, South Korea
Background: Patients with mucinous gastric carcinoma (MGC) usually have a poor prognosis, largely due to the advanced stage of disease. In this study, we evaluated the effects of c-MYC amplification on tumor stage and disease-specific survival of 128 patients with MGC and compared the results with those of 302 patients with non-mucinous gastric carcinoma (non-MGC). Patients and Methods: Two-color fluorescence in situ hybridization (FISH) for c-MYC was performed on 430 GC samples. Real-time quantitative polymerase chain reaction (q-PCR) analysis for c-MYC was also performed after tumor microdissection. Results: c-MYC amplification was found in 10.2% of MGCs and 6.0% of non-MGCs. c-MYC amplification was more frequently found in MGCs of higher tumor stage than in MGCs of lower stage (p=0.038). c-MYC amplification in MGC was correlated with greater invasion depth (p=0.007). The mean survival time of patients with c-MYC amplification was shorter than that of patients without c-MYC amplification in MGC. Real-time q-PCR results showed that the calculated c-MYC/GAPDH ratios were higher in c-MYC-amplified MGC than in c-MYC-non-amplified MGC. Conclusion: This study showed that c-MYC amplification in MGC is highly correlated with advanced stage and deeply invasive MGC. This suggests that c-MYC amplification in MGC could be a possible genetic alteration contributing to the frequent presentation of advanced-stage MGC.