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E3B1/ABI-1 isoforms are down-regulated in cancers of human gastrointestinal tract. | LitMetric

AI Article Synopsis

  • The study investigates the expression of E3B1/ABI-1 protein in various solid tumors, including esophageal, gastro-esophageal junction, and colorectal cancers, using techniques like Western Blotting and Immunofluorescence Staining.
  • E3B1/ABI-1 is present in a phosphorylated form, with variations in size based on the level of phosphorylation, indicating its complex nature in cellular processes.
  • Findings show a significant decrease in E3B1/ABI-1 expression across all cancer types studied, suggesting its down-regulation could be important for tumor progression and prognosis, regardless of patient demographics.

Article Abstract

The expression of E3B1/ABI-1 protein and its role in cancer progression and prognosis are largely unknown in the majority of solid tumors. In this study, we examined the expression pattern of E3B1/ABI-1 protein in histologically confirmed cases of esophageal (squamous cell carcinoma and adenocarcinoma), gastro-esophageal junction, colorectal cancers and corresponding normal tissues freshly resected from a cohort of 135 patients, by Western Blotting and Immunofluorescence Staining. The protein is present in its phosphorylated form in cells and tissues. Depending on the extent of phosphorylation it is either present in hyper-phosphorylated (M. Wt. 72 kDa) form or in hypo-phosphorylated form (M. Wt. 68 kDa and 65 kDa). A thorough analysis revealed that expression of E3B1/ABI-1 protein is significantly decreased in esophageal, gastro-esophageal junction and colorectal carcinomas irrespective of age, gender, dietary and smoking habits of the patients. The decrease in expression of E3B1/ABI-1 was consistently observed for all the three isoforms. However, the decrease in the expression of isoforms varied with different forms of cancers. Down-regulation of E3B1/ABI-1 expression in human carcinomas may play a critical role in tumor progression and in determining disease prognosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3826811PMC
http://dx.doi.org/10.3233/DMA-2011-0881DOI Listing

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