Immunohistochemical investigation of GST-M, GST-P, and TP53 gene expression in obesity patients under laparoscopic sleeve gastrectomy

Tissue Cell. 2026 Feb:98:103143. doi: 10.1016/j.tice.2025.103143. Epub 2025 Sep 16.

Abstract

Obesity is linked to increased oxidative stress, contributing to various comorbidities. Glutathione S-transferases (GSTs) enzymes and tumor suppressor protein 53 (TP53) are key regulators of oxidative stress. This study aimed to examine the expression of GST-M, GST-P, and TP53 in sleeve gastrectomy tissues of obese patients. In this retrospective study, 126 obese patients who underwent sleeve gastrectomy were analyzed. Immunohistochemical staining assessed the expression of GST-M, GST-P, and TP53 in sleeve gastrectomy tissue samples. Correlation between protein expression and association with demographic, clinical, and serological data was examined. GST-P and GST-M exhibited low expression (absent/weak), while TP53 showed significantly higher expression in the sleeve gastrectomy tissue of patients with obesity. A positive and significant correlation was identified between GST-M and TP53 staining levels, while GST-P expression level did not display any correlation with GST-M and TP53. Distinct patterns of protein expression for GST-P, GST-M, and TP53 in the sleeve gastrectomy tissues of obesity patients. TP53 plays a key role in oxidative stress regulation in obesity, whereas GST-M and GST-P appear less effective.

Keywords: GST-M; GST-P; Obesity; Oxidative stress; Sleeve gastrectomy; TP53.

MeSH terms

  • Adult
  • Female
  • Gastrectomy* / methods
  • Glutathione S-Transferase pi* / genetics
  • Glutathione S-Transferase pi* / metabolism
  • Glutathione Transferase* / biosynthesis
  • Glutathione Transferase* / genetics
  • Glutathione Transferase* / metabolism
  • Humans
  • Immunohistochemistry
  • Laparoscopy*
  • Male
  • Middle Aged
  • Obesity* / genetics
  • Obesity* / metabolism
  • Obesity* / pathology
  • Obesity* / surgery
  • Oxidative Stress
  • Retrospective Studies
  • Tumor Suppressor Protein p53* / biosynthesis
  • Tumor Suppressor Protein p53* / genetics
  • Tumor Suppressor Protein p53* / metabolism

Substances

  • Tumor Suppressor Protein p53
  • Glutathione Transferase
  • Glutathione S-Transferase pi
  • TP53 protein, human