Shanghai Institute of Immunology, Institutes of Medical Sciences, Shanghai Jiao Tong University School of Medicine (SJTUSM), Shanghai, China.
BMC Cancer. 2010 May 7;10:184. doi: 10.1186/1471-2407-10-184.
Insulin-like growth factor-I receptor (IGFIR) has been shown to regulate the tumor development. The objective of the current study is to determine the association of IGFIR with lymph node metastasis and to explore the related mechanism in human colorectal cancer in clinic.
In a random series of 98 colorectal cancer patients, the expressions of IGFIR, vascular endothelial growth factor (VEGF) and VEGF-C were investigated by immunohistochemistry, and the association of these expressions with lymph node metastasis was statistically analyzed. The expressions of VEGF and VEGF-C in colorectal cancer cells stimulated with IGF-I were also examined by real-time quantitative reverse transcription-polymerase chain reaction and enzyme-linked immunosorbent assay.
Higher rates of IGFIR (46%), VEGF (53%), and VEGF-C (46%) expression were found in colorectal cancer tissues than in normal and colorectal adenoma tissues. These expressions were significantly associated with clinicopathologic factors and lymph node status. We also found the concomitant high expressions of IGFIR/VEGF (P < 0.001) and IGFIR/VEGF-C (P = 0.001) had a stronger correlation with lymph node metastasis than did each alone or both low expressions. In addition, IGF-I could effectively induce the VEGF and VEGF-C mRNA expression and protein secretion in colorectal cancer cells expressing IGFIR molecules. Moreover, Patients who had strong staining for IGFIR, VEGF and VEGF-C showed significantly less favorable survival rates compared with patients who had low staining for these molecules (P < 0.001). The survival rates of patients who were both high expression of IGFIR/VEGF and IGFIR/VEGF-C also were significantly lower compared with patients who were negative or one of high expression of these molecules (P < 0.001).
Together the findings indicated for the first time that simultaneous examination of the expressions of IGFIR, VEGF and VEGF-C will benefit the diagnosis of lymph node metastasis in order to assay the prognosis and determine the treatment strategy in patients with colorectal cancer undergoing surgery.
胰岛素样生长因子-I 受体(IGFIR)已被证明可调节肿瘤的发展。本研究的目的是确定 IGFIR 与淋巴结转移的相关性,并在临床中探讨其在人结直肠癌中的相关机制。
在 98 例随机结直肠癌患者中,采用免疫组织化学法检测 IGFIR、血管内皮生长因子(VEGF)和 VEGF-C 的表达,并对其与淋巴结转移的相关性进行统计学分析。还通过实时定量逆转录-聚合酶链反应和酶联免疫吸附试验检测 IGF-I 刺激的结直肠癌细胞中 VEGF 和 VEGF-C 的表达。
结直肠癌组织中 IGFIR(46%)、VEGF(53%)和 VEGF-C(46%)的表达率均高于正常和结直肠腺瘤组织,且与临床病理因素和淋巴结状态显著相关。我们还发现 IGFIR/VEGF(P<0.001)和 IGFIR/VEGF-C(P=0.001)的同时高表达与淋巴结转移的相关性强于单独高表达或两者均低表达。此外,IGF-I 可有效诱导表达 IGFIR 分子的结直肠癌细胞中 VEGF 和 VEGF-C 的 mRNA 表达和蛋白分泌。此外,与这些分子低表达的患者相比,IGFIR、VEGF 和 VEGF-C 染色强的患者的生存状况明显较差(P<0.001)。IGFIR/VEGF 和 IGFIR/VEGF-C 均高表达的患者的生存状况也明显低于这些分子阴性或其中一种高表达的患者(P<0.001)。
这些发现首次表明,同时检测 IGFIR、VEGF 和 VEGF-C 的表达有助于诊断淋巴结转移,以便评估结直肠癌患者手术后的预后并确定治疗策略。