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CXCR-4表达在口腔鳞状细胞癌中的预后意义

Prognostic significance of CXCR-4 expression in oral squamous cell carcinoma.

作者信息

Lee Jae-Il, Jin Bo-Hyong, Kim Mi-Ae, Yoon Hye-Jung, Hong Sam-Pyo, Hong Seong-Doo

机构信息

Department of Oral Pathology, School of Dentistry, Seoul National University, Seoul, Korea.

出版信息

Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009 May;107(5):678-84. doi: 10.1016/j.tripleo.2008.12.047. Epub 2009 Mar 9.

Abstract

OBJECTIVE

We investigated the prognostic significance of CXC chemokine receptor CXCR-4 expression in patients with oral squamous cell carcinoma (OSCC) and its relationship with matrix metalloproteinase 2 (MMP-2), MMP-9, and Ki-67 expression.

STUDY DESIGN

The CXCR-4, MMP-2, MMP-9, and Ki-67 expression was assessed immunohistochemically in 74 OSCC patients. The results were analyzed in connection with clinicopathologic factors.

RESULTS

The CXCR-4 expression was positive in 45 cases and significantly correlated with lymph node metastasis (P = .037), MMP-9 expression (P = .025), and Ki-67 expression (P = .001). Univariate analysis showed that CXCR-4 expression, MMP-9 expression, Ki-67 expression, tumor size, lymph node metastasis, clinical stage, and recurrence positively correlated with prognosis. Multivariate analysis indicated that CXCR-4 expression was an independent prognostic factor for poor survival in patients with OSCC.

CONCLUSION

Expression of CXCR-4 is a significant prognostic indicator for poor survival in patients with OSCC and correlates with expression of MMP-9 and Ki-67. The inhibition of CXCR-4 represents a possible molecular approach to the treatment of OSCC.

摘要

目的

我们研究了CXC趋化因子受体CXCR - 4表达在口腔鳞状细胞癌(OSCC)患者中的预后意义及其与基质金属蛋白酶2(MMP - 2)、MMP - 9和Ki - 67表达的关系。

研究设计

采用免疫组织化学方法评估74例OSCC患者的CXCR - 4、MMP - 2、MMP - 9和Ki - 67表达。并结合临床病理因素分析结果。

结果

45例患者CXCR - 4表达呈阳性,且与淋巴结转移(P = .037)、MMP - 9表达(P = .025)和Ki - 67表达(P = .001)显著相关。单因素分析显示,CXCR - 4表达、MMP - 9表达、Ki - 67表达、肿瘤大小、淋巴结转移、临床分期和复发与预后呈正相关。多因素分析表明,CXCR - 4表达是OSCC患者生存不良的独立预后因素。

结论

CXCR - 4表达是OSCC患者生存不良的重要预后指标,且与MMP - 9和Ki - 67表达相关。抑制CXCR - 4可能是治疗OSCC的一种分子方法。

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