Prognostic significance of the expression of Smad4 and Smad7 in human gastric carcinomas

被引:57
|
作者
Kim, YH
Lee, HS
Lee, HJ
Hur, K
Kim, WH
Bang, YJ
Kim, SJ
Lee, KU
Choe, KJ
Yang, HK
机构
[1] Seoul Natl Univ, Coll Med, Dept Surg, Seoul 110744, South Korea
[2] Seoul Natl Univ, Coll Med, Dept Pathol, Seoul 110744, South Korea
[3] Seoul Natl Univ, Coll Med, Natl Res Lab Canc Epigenet, Seoul 110744, South Korea
[4] Seoul Natl Univ, Coll Med, Canc Res Inst, Seoul 110744, South Korea
[5] NCI, Lab Cell Regulat & Carcinogenesis, Bethesda, MD 20892 USA
关键词
gastric carcinoma; prognostic factor; Smad4; Smad7; transforming growth factor-beta;
D O I
10.1093/annonc/mdh131
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Transforming growth factor-beta (TGF-beta) modulates the growth and function of many cells, including those with malignant transformation. Smad proteins have been identified as major components in the intracellular signaling of TGF-beta family members. Patients and methods: To clarify the correlations between clinicopathologic profiles and the patient's survival, the expression of common mediator Smad (Smad4) and inhibitory Smad (Smad7) were evaluated immunohistochemically in 304 consecutive gastric carcinomas using the tissue array method. Results: Positive Smad4 expression was observed in 266 (87.5%) tumors and positive Smad7 expression in 98 (32.2%) tumors. The prognosis of patients with a Smad4-positive tumor was significantly better than that of the patients with a negative tumor. The survival rate was significantly higher in patients with negative Smad7 expression than those with positive Smad7 expression. In subgroup analysis according to TNM (tumour-node-metastasis) stage, both Smad4 and Smad7 showed most significant prognostic differences in stage I gastric cancer patients. Multivariate analysis indicated that tumor size, depth of invasion, lymph node metastasis and Smad7 expression were independent prognostic factors. Conclusion: Enhanced expression of the TGF-beta signaling inhibitor Smad7 may present one of the novel mechanisms of TGF-beta resistance in human gastric carcinomas.
引用
收藏
页码:574 / 580
页数:7
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