Lu Fenying, Chen Weichang, Jiang Tingwang, Cheng Cuie, Wang Bin, Lu Zhiping, Huang Guojin, Qiu Jiaming, Wei Wei, Yang Ming, Huang Xia
Department of Gastroenterology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215006, P.R. China.
Department of Gastroenterology, The Second People's Hospital of Changshu, Suzhou, Jiangsu 215500, P.R. China.
Exp Ther Med. 2022 Apr;23(4):252. doi: 10.3892/etm.2022.11177. Epub 2022 Feb 1.
The ectopic expression of insulin-like growth factor 2 mRNA-binding protein 2 (IGF2BP2) has been demonstrated to facilitate tumorigenesis and induce proliferation in a various types of cancer. However, the role of IGF2BP2 in esophageal squamous cell carcinoma (ESCC) has yet been fully elucidated. In this regard, the current study assessed the expression patterns and clinical significance of IGF2BP2 in 94 Chinese patients diagnosed with ESCC. Immunohistochemistry and reverse transcription-quantitative PCR assays were employed to assess IGF2BP2 expression in ESCC tissues compared with adjacent healthy tissues. The results revealed that the protein expression of IGF2BP2 was substantially upregulated in ESCC tissues compared with adjacent ESCC tissues. More specifically, higher IGF2BP2 expression strongly associated with tumor node metastasis stage, lymphatic infiltration and lymph node metastasis. Using two ESCC cell lines (TE-1 and TE-10), the inhibition of IGF2BP2 expression by small interfering RNA was proven to induce apoptosis and suppress proliferation, migration and cell cycle progression . Collectively, the present findings indicated that IGF2BP2 may serve a major role in the development of ESCC carcinogenesis. The present study may be helpful in the design of potential drug targets in the treatment of ESCC.
胰岛素样生长因子2 mRNA结合蛋白2(IGF2BP2)的异位表达已被证明可促进多种癌症的肿瘤发生并诱导增殖。然而,IGF2BP2在食管鳞状细胞癌(ESCC)中的作用尚未完全阐明。在这方面,当前研究评估了94例诊断为ESCC的中国患者中IGF2BP2的表达模式及其临床意义。采用免疫组织化学和逆转录定量PCR分析评估ESCC组织与相邻健康组织中IGF2BP2的表达。结果显示,与相邻的ESCC组织相比,ESCC组织中IGF2BP2的蛋白表达显著上调。更具体地说,较高的IGF2BP2表达与肿瘤淋巴结转移分期、淋巴浸润和淋巴结转移密切相关。使用两种ESCC细胞系(TE-1和TE-10),经证实,小干扰RNA抑制IGF2BP2表达可诱导细胞凋亡并抑制增殖、迁移和细胞周期进程。总体而言,目前的研究结果表明,IGF2BP2可能在ESCC致癌过程中起主要作用。本研究可能有助于设计ESCC治疗中的潜在药物靶点。