AI Article Synopsis

  • The study focuses on the role of IGF2BP2, a protein linked to cancer growth, specifically in esophageal squamous cell carcinoma (ESCC) among 94 Chinese patients.
  • It found that IGF2BP2 was significantly more expressed in ESCC tissues than in adjacent healthy tissues, correlating with advanced tumor stages and metastasis.
  • Silencing IGF2BP2 in ESCC cell lines led to decreased cell growth and increased cell death, suggesting that IGF2BP2 could be a key target for potential ESCC treatments.

Article 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 . 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8855499PMC
http://dx.doi.org/10.3892/etm.2022.11177DOI Listing

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