Differential Expression of α-Enolase in Clinical Gastric Tissues and Cultured Normal/Cancer Cells in Response to Helicobacter pylori Infection and cagA Transfection

Medicina (Kaunas). 2022 Oct 14;58(10):1453. doi: 10.3390/medicina58101453.

Abstract

Background and Objectives: The role of α-enolase (ENO1) in Helicobacter pylori-related gastric lesions might be a critical factor in the pathogenesis, but remains undefined. Materials and Methods: This study investigated the differential expression of α-enolase in clinical gastric specimens and cultured normal/cancer cells in response to H. pylori (cagA+) infection and cagA transfection using qPCR, Western blots and histochemical methods. Results: A total of 172 gastric specimens were collected from 142 patients, the former comprising chronic superficial gastritis (CSG), precancerous diseases (PCDs, including atrophic gastritis, intestinal metaplasia and dysplasia) and gastric cancer (GC) cases. Among the CSG and PCD cases, the H. pylori-infected group had significantly elevated ENO1 mRNA levels compared with the uninfected group. In the GC cases, differential ENO1 expressions were detected between the cancer tissues and the paracancerous tissues. Notably, significant difference was first detected between the GC cell (AGS) and the normal cell (GES-1) as a response of ENO1 to H. pylori infection and cagA transfection. Conclusions: This report reveals that ENO1 expression is associated with H. pylori infection, cagA transfection, co-culture duration, multiplicity of infection, gastric normal/cancerous cell lines and cellular differentiation. The findings may be crucial bases for further ascertaining H. pylori pathogenic mechanism and formulating novel therapeutic and diagnostic strategies.

Keywords: Helicobacter pylori; cytotoxin associated gene A; gastric cancer; precancer lesion; α-enolase.

MeSH terms

  • Cell Line
  • Gastric Mucosa / metabolism
  • Helicobacter Infections* / complications
  • Helicobacter pylori* / genetics
  • Humans
  • Phosphopyruvate Hydratase / genetics
  • Phosphopyruvate Hydratase / metabolism
  • Precancerous Conditions* / complications
  • Precancerous Conditions* / genetics
  • Precancerous Conditions* / metabolism
  • RNA, Messenger / metabolism
  • Stomach Neoplasms* / complications
  • Stomach Neoplasms* / genetics
  • Transfection

Substances

  • Phosphopyruvate Hydratase
  • RNA, Messenger