Zhang Nian-Hua, Li Jie, Li Yin, Zhang Xin-Tao, Liao Wen-Ting, Zhang Jun-Yi, Li Rong, Luo Rong-Cheng
Department of Oncology, Nanfang Hospital, Southern Medical University, Guangzhou 510515;
Exp Ther Med. 2012 Jun;3(6):973-982. doi: 10.3892/etm.2012.527. Epub 2012 Mar 27.
Although CXCR4 and CD133 have been implicated in the metastatic process of malignant tumors, the clinicopathological significance of their expression in human colon cancer is not fully understood. The present study aimed to examine the expression of the CXCR4 and CD133 proteins in cases of stage II or III colon cancer and the related lymph nodes and to investigate the clinical and prognostic significance of these proteins in colon cancer. Immunohistochemical analysis was performed to examine CXCR4 and CD133 protein expression in paraffin-embedded stage II or III primary colon cancer tissues and matched lymph nodes. The correlation between the expression of the two proteins and clinicopathological parameters and the patient 5-year survival was analyzed. CXCR4 expression was detected in 74 of the 125 tumors (59.2%) and CD133 expression was detected in 45 (36.0%). The co-expression of CXCR4 and CD133 (both CXCR4 and CD133 were positive) was detected in 29 of the 125 tumors (23.2%). Compared with the other combinations, the co-expression of the CXCR4 and CD133 proteins was significantly associated with American Joint Committee on Cancer (AJCC) stage (P=0.029) and lymph node status (P=0.020). Log-rank analysis revealed that AJCC stage (P=0.014), lymph node status (P=0.011), CXCR4 expression (P=0.023), CD133 expression (P=0.034) and the co-expression of the CXCR4 and CD133 proteins (P=0.003) were significant prognostic indicators for the overall survival of patients. The results of the present study show that the co-expression of the CXCR4 and CD133 proteins is a risk factor for poor overall survival in stage II or III colon cancer patients, indicating that the co-expression of the CXCR4 and CD133 proteins contributes to the progression of colon cancer.
尽管CXCR4和CD133与恶性肿瘤的转移过程有关,但其在人类结肠癌中表达的临床病理意义尚未完全明确。本研究旨在检测II期或III期结肠癌病例及其相关淋巴结中CXCR4和CD133蛋白的表达情况,并探讨这些蛋白在结肠癌中的临床及预后意义。采用免疫组织化学分析法检测石蜡包埋的II期或III期原发性结肠癌组织及其匹配淋巴结中CXCR4和CD133蛋白的表达。分析了这两种蛋白的表达与临床病理参数及患者5年生存率之间的相关性。125例肿瘤中有74例(59.2%)检测到CXCR4表达,45例(36.0%)检测到CD133表达。125例肿瘤中有29例(23.2%)检测到CXCR4和CD133共表达(CXCR4和CD133均为阳性)。与其他组合相比,CXCR4和CD133蛋白的共表达与美国癌症联合委员会(AJCC)分期(P=0.029)和淋巴结状态(P=0.020)显著相关。对数秩分析显示,AJCC分期(P=0.014)、淋巴结状态(P=0.011)、CXCR4表达(P=0.023)、CD133表达(P=0.034)以及CXCR4和CD133蛋白的共表达(P=0.003)是患者总生存的重要预后指标。本研究结果表明,CXCR4和CD133蛋白的共表达是II期或III期结肠癌患者总生存不良的危险因素,提示CXCR4和CD133蛋白的共表达促进了结肠癌的进展。