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Raf-1 激酶抑制蛋白表达降低预示食管鳞癌区域淋巴结转移和生存时间缩短。

Reduced expression of Raf-1 kinase inhibitory protein predicts regional lymph node metastasis and shorter survival in esophageal squamous cell carcinoma.

机构信息

Aerospace Medical Research Center, Aerospace Medical Center, Republic of Korea Air Force, PO Box 335-21, Ssangsu-ri, Namil-myeon, Cheongwon-gun, 363-842 Chungcheongbuk-do, Republic of Korea.

出版信息

Pathol Res Pract. 2012 May 15;208(5):292-9. doi: 10.1016/j.prp.2012.02.011. Epub 2012 Mar 29.

DOI:10.1016/j.prp.2012.02.011
PMID:22464151
Abstract

Raf-1 kinase inhibitory protein (RKIP), a suppressor of metastasis, is associated inversely with the progression and metastasis of human malignancies. The present study evaluated relationships between RKIP expression and metastatic potential, clinicopathological characteristics and patient outcome in esophageal squamous cell carcinoma (ESCC). We examined tissue specimens from 138 patients with thoracic ESCC. Using immunohistochemistry, RKIP expression was detected in ESCC in situ, primary ESCC and nodal metastatic ESCC. RKIP expression was reduced in 28.9% (13/45) of ESCC in situ, in 50.0% (69/138) of primary ESCC and in 71.4% (65/91) of nodal metastatic ESCC. These levels of RKIP down-regulation differed significantly. RKIP expression was associated inversely with histological grade (P=0.008), pathological T stage (P=0.044), lymphatic invasion (P=0.019), regional lymph node metastasis (LNM; P=0.002) and stage (P=0.041). Pathological T stage (P=0.001), lymphatic invasion (P<0.001) and reduced RKIP expression (P=0.039) were independent predictors of regional LNM in ESCC. In addition, the postoperative survival of patients with RKIP-reduced ESCC was significantly shorter than for patients with RKIP-positive ESCC (P=0.004). Reduced RKIP expression in ESCC correlated with advanced disease, regional LNM and poor prognosis. RKIP expression may serve as a novel clinical biomarker in patients with ESCC.

摘要

Raf-1 激酶抑制蛋白(RKIP)是一种转移抑制因子,与人类恶性肿瘤的进展和转移呈负相关。本研究评估了 RKIP 表达与食管鳞癌(ESCC)转移潜能、临床病理特征和患者预后的关系。我们检测了 138 例胸段 ESCC 患者的组织标本。应用免疫组织化学方法,检测 ESCC 原位、原发 ESCC 和淋巴结转移性 ESCC 中 RKIP 的表达。结果显示,ESCC 原位组织中 RKIP 表达缺失率为 28.9%(13/45),原发 ESCC 为 50.0%(69/138),淋巴结转移性 ESCC 为 71.4%(65/91)。RKIP 下调程度差异有统计学意义。RKIP 表达与组织学分级(P=0.008)、病理 T 分期(P=0.044)、淋巴管浸润(P=0.019)、区域淋巴结转移(LNM;P=0.002)和分期(P=0.041)呈负相关。病理 T 分期(P=0.001)、淋巴管浸润(P<0.001)和 RKIP 表达缺失(P=0.039)是 ESCC 区域 LNM 的独立预测因子。此外,RKIP 表达缺失的 ESCC 患者的术后生存时间明显短于 RKIP 阳性的 ESCC 患者(P=0.004)。ESCC 中 RKIP 表达缺失与疾病进展、区域 LNM 和不良预后相关。RKIP 表达缺失可能成为 ESCC 患者的一个新的临床标志物。

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