Department of Pathology, Tianjin Medical University, Tianjin, China.
J Exp Clin Cancer Res. 2010 Feb 24;29(1):16. doi: 10.1186/1756-9966-29-16.
The chemokine receptors CXCR4 and CCR7 play an important role in cancer invasion and metastasis. This study investigated the expression of CXCR4, CCR7, CXCL12, CCL21, and EGFR to illustrate the role of these biomarkers in breast cancer metastasis and prognosis.
The CXCR4, CCR7, CXCL12, CCL21, and EGFR biomarkers were analyzed along with ER, PR, and HER-2/neu in breast cancer tissue microarray (TMA) specimens, including 200 primary breast cancer specimens by immunohistochemistry. Corresponding lymph nodes from the same patients were also examined using the same method.
Together with their CXCL12 and CCL21 ligands, CXCR4 and CCR7 were significantly highly expressed in tumor cells with lymph node (LN) metastasis. Similarly, EGFR was expressed highly in tumors with LN metastasis. The ligands were especially expressed in metastatic tumors than in primary tumors from the same patients. Moreover, the expression of both CXCR4 accompanied by CCR7 and CXCL12 accompanied by CCL21 were up-regulated. Kaplan-Meier survival analysis revealed that patients exhibiting high CXCR4, CCR7, and EGFR expression experienced a shorter survival period compared with those with low expression.
The expression of CXCR4, CCR7, and EGFR may be associated with LN metastasis. Moreover, the expression of these receptors can serve as an indicator of undesirable prognosis in patients with breast cancer.
趋化因子受体 CXCR4 和 CCR7 在癌症侵袭和转移中发挥重要作用。本研究调查了 CXCR4、CCR7、CXCL12、CCL21 和 EGFR 的表达,以阐明这些生物标志物在乳腺癌转移和预后中的作用。
通过免疫组织化学分析包括 200 例原发性乳腺癌组织微阵列(TMA)标本中的 CXCR4、CCR7、CXCL12、CCL21 和 EGFR 生物标志物,以及同一患者的相应淋巴结。
与淋巴结(LN)转移的肿瘤细胞一起,CXCR4 和 CCR7 及其 CXCL12 和 CCL21 配体表达显著升高。同样,EGFR 在具有 LN 转移的肿瘤中表达较高。配体在转移性肿瘤中的表达明显高于同一患者的原发性肿瘤。此外,CXCR4 伴随 CCR7 和 CXCL12 伴随 CCL21 的表达均上调。Kaplan-Meier 生存分析显示,高表达 CXCR4、CCR7 和 EGFR 的患者与低表达患者相比,生存时间更短。
CXCR4、CCR7 和 EGFR 的表达可能与 LN 转移有关。此外,这些受体的表达可以作为乳腺癌患者不良预后的指标。