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CXCL12及其受体CXCR4在食管鳞状细胞癌中的表达

Expression of CXCL12 and its receptor CXCR4 in esophageal squamous cell carcinoma.

作者信息

Sasaki Ken, Natsugoe Shoji, Ishigami Sumiya, Matsumoto Masataka, Okumura Hiroshi, Setoyama Tetsuro, Uchikado Yasuto, Kita Yoshiaki, Tamotsu Kiyokazu, Hanazono Koichi, Owaki Tetsuhiro, Aikou Takashi

机构信息

Department of Surgical Oncology and Digestive Surgery, Field of Oncology, Course of Advanced Therapeutics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima 890-8520, Japan.

出版信息

Oncol Rep. 2009 Jan;21(1):65-71.

Abstract

The chemokine CXCL12, also known as stromal cell-derived factor-1 and its receptor CXCR4 have been shown to play prominent roles in regulating the directional migration and proliferation of various types of cancer cells during the metastatic process. However, few researchers have examined the expression of CXCL12 and CXCR4 and their prognostic value in patients with esophageal squamous cell carcinoma (ESCC). We investigated immunohistochemically the relationship between CXCL12 and CXCR4 expression and clinicopathological factors including prognosis in surgical specimens of primary tumors in 214 patients with ESCC. The positive expression rate of CXCL12 was 53.7% and that of CXCR4 was 84.6%. Positive CXCL12 expression was significantly correlated with lymph node metastasis, tumor stage, gender and lymphatic invasion. The overall and disease-free survival rate was significantly lower in patients with positive CXCL12 expression than in those with negative CXCL12 expression. The expression of CXCR4 had no correlation with clinicopathological variables and prognosis. We showed that positive CXCL12 expression was related to a greater degree to tumor development, compared with CXCR4 expression. Evaluation of CXCL12 expression is useful for determining tumor properties, including nodal metastasis and prognosis in patients with ESCC.

摘要

趋化因子CXCL12,也被称为基质细胞衍生因子-1,及其受体CXCR4,已被证明在转移过程中对调节各类癌细胞的定向迁移和增殖起着重要作用。然而,很少有研究人员检测过CXCL12和CXCR4在食管鳞状细胞癌(ESCC)患者中的表达及其预后价值。我们采用免疫组织化学方法研究了214例ESCC患者原发性肿瘤手术标本中CXCL12和CXCR4表达与包括预后在内的临床病理因素之间的关系。CXCL12的阳性表达率为53.7%,CXCR4的阳性表达率为84.6%。CXCL12阳性表达与淋巴结转移、肿瘤分期、性别及淋巴管浸润显著相关。CXCL12阳性表达患者的总生存率和无病生存率显著低于CXCL12阴性表达患者。CXCR4的表达与临床病理变量及预后无关。我们发现,与CXCR4表达相比,CXCL12阳性表达与肿瘤发展的关联程度更大。评估CXCL12表达有助于确定ESCC患者的肿瘤特性,包括淋巴结转移和预后。

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