| Literature DB >> 35261624 |
Fenying Lu1,2, Weichang Chen1, Tingwang Jiang3, Cuie Cheng2, Bin Wang2, Zhiping Lu2, Guojin Huang2, Jiaming Qiu4, Wei Wei4, Ming Yang5, Xia Huang2.
Abstract
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 in vitro. 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.Entities:
Keywords: downregulation; esophageal-squamous cell carcinoma; insulin-like growth factor 2 mRNA-binding protein 2; migration; proliferation
Year: 2022 PMID: 35261624 PMCID: PMC8855499 DOI: 10.3892/etm.2022.11177
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447