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Regulation of pro-apoptotic and anti-apoptotic factors in obesity-related esophageal adenocarcinoma. | LitMetric

AI Article Synopsis

  • Obesity is linked to esophageal adenocarcinoma (EAC), with inflammation from obesity contributing to insulin resistance and a higher risk of developing EAC.
  • The study analyzed tissue samples from 23 patients to assess the levels of various pro-apoptotic and anti-apoptotic factors that could influence EAC progression.
  • Findings revealed that EAC and Barrett's esophagus showed reduced pro-apoptotic factors and increased anti-apoptotic factors, suggesting that obesity-related changes in these mediators could promote EAC development.

Article Abstract

Background: Obesity is a risk factor for esophageal adenocarcinoma (EAC). It was reported that obesity -associated inflammation correlates with insulin resistance and increased risk of EAC. The objective of the study is to investigate the role of obesity associated inflammatory mediators in the development of EAC.

Methods: We included 23 obese and nonobese patients with EAC or with or without Barrett's esophagus (BE) after IRB approval. We collected 23 normal, 10 BE, and 19 EAC tissue samples from endoscopy or esophagectomy. The samples were analyzed for the expression levels of pro-apoptotic and anti-apoptotic factors, PKC-δ, cIAP2, FLIP, IGF-1, Akt, NF-kB and Ki67 by immunofluorescence and RT-PCR. We compared the expression levels between normal, BE, and EAC tissue using Students' t-test between two groups.

Results: Our results showed decreased gene and protein expression of pro-apoptotic factors (bad, bak and bax) and increased expression of anti-apoptotic factors (bcl-2, Bcl-xL) in BE and EAC compared to normal tissues. There was increased gene and protein expression of PKC-δ, cIAP2, FLIP, NF-kB, IGF-1, Akt, and Ki67 in BE and EAC samples compared to normal esophagus. Further, an increased folds changes in mRNA expression of proapoptotic factors, antiapoptotic factors, PKC-δ, IGF-1, Akt, and Ki-67 was associated with obesity.

Conclusion: Patients with EAC had increased expression of cIAP2 and FLIP, and PKC-δ which is associated with inhibition of apoptosis and possible progression of esophageal adenocarcinoma.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11470870PMC
http://dx.doi.org/10.1007/s11033-024-09931-6DOI Listing

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