Neoplasma. 2017;64(1):101-107. doi: 10.4149/neo_2017_112.
To explore how Tim-3 is expressed and how its expression influences invasion and metastasis of colorectal cancer (CRC) cells. A total of 188 CRC patients were prospectively collected for this study. Meanwhile, 135 normal controls were incorporated during the same period. Intestinal samples of the CRC radical cancerous tissues, paracancerous tissues ( 5.0 cm beyond the cancer tissue) were collected for the following experiment. Furthermore, peripheral venous blood samples (10 ml) were collected from each subject. Immunohistochemical analysis, quantitative real-time polymerase chain reaction (RT-qPCR) and western blot were performed for the detection of Tim-3 in different tissues. The immunohistochemical staining results showed that a positive Tim-3 signal was localized in the cytoplasm and nucleus, observed as yellow or brown granules. Tim-3 was largely expressed in colon carcinoma tissues and normal colon mucosa tissues but was rarely expressed in the cell membrane. RT-qPCR results indicated that Tim-3 mRNA levels were significantly lower in CRC tissues than in paracancerous tissues and normal colon mucosa tissues. A trend of decreased Tim-3 mRNA levels was also found in the paracancerous tissues compared with the normal colon mucosa tissues (all P < 0.05). Western blot results revealed reduced Tim-3 protein expression in CRC tissues compared with normal colon mucosa tissues and paracancerous tissues, and Tim-3 protein expression was much lower in the paracancerous tissues than in the normal colon mucosa tissues (all P < 0.05). Furthermore, obviously lower Tim-3 mRNA levels were found in the poorly differentiated CRC patients and in those with lymph node metastasis and distant metastasis (all P < 0.05). Collectively, Tim-3 expression was mainly located in the cytoplasm and nucleus, showing down-regulated expression in colon carcinoma tissues compared with normal and paracancerous tissues. Reduced Tim-3 expression may promote CRC invasion and metastasis providing a medical reference for the treatment of CRC.
探讨 Tim-3 的表达及其表达对结直肠癌(CRC)细胞侵袭转移的影响。
前瞻性收集 188 例 CRC 患者作为研究对象,同时纳入同期 135 例正常对照者。收集 CRC 根治性癌组织、癌旁组织(癌组织外 5.0 cm)肠组织,每位患者采集外周静脉血 10 ml。采用免疫组化分析、实时定量聚合酶链反应(RT-qPCR)和 Western blot 检测不同组织中 Tim-3 的表达。
免疫组化染色结果显示,Tim-3 阳性信号定位于细胞质和细胞核,呈黄色或棕色颗粒。Tim-3 在结肠腺癌组织和正常结肠黏膜组织中大量表达,但在细胞膜上很少表达。RT-qPCR 结果显示,CRC 组织中 Tim-3 mRNA 水平明显低于癌旁组织和正常结肠黏膜组织。癌旁组织 Tim-3 mRNA 水平也呈下降趋势,与正常结肠黏膜组织比较差异有统计学意义(均 P<0.05)。Western blot 结果显示,CRC 组织中 Tim-3 蛋白表达低于正常结肠黏膜组织和癌旁组织,癌旁组织中 Tim-3 蛋白表达明显低于正常结肠黏膜组织(均 P<0.05)。此外,低分化 CRC 患者、有淋巴结转移和远处转移的患者 Tim-3 mRNA 水平明显降低(均 P<0.05)。
Tim-3 表达主要位于细胞质和细胞核,在结肠癌组织中表达下调,其低表达可能促进 CRC 的侵袭和转移,为 CRC 的治疗提供了医学参考。