Involvement of ER-α36 in the malignant growth of gastric carcinoma cells is associated with GRP94 overexpression

Histopathology. 2013 Sep;63(3):325-33. doi: 10.1111/his.12171. Epub 2013 Jul 8.

Abstract

Aims: This study aimed to examine the involvement of glucose-regulated protein 94 (GRP94) in oestrogen receptor-α36 (ER-α36)-mediated oestrogen signalling in gastric cancer development.

Methods and results: A total of 130 formalin-fixed and paraffin-embedded gastric tumour samples with corresponding normal gastric and tumour-adjacent tissues were used. High levels of GRP94 expression (2+ or 3+) were observed in 109 of 130 gastric carcinomas (83.85%) by immunohistochemistry, and in 13 of 18 tumour specimens (72.22%) with Western blot analysis. GRP94 expression was correlated positively with gender, tumour stage, lymph node metastasis and ER-α36 expression (P < 0.05). Oestrogen treatment up-regulated both GRP94 and ER-α36 expression in gastric cancer SGC7901 cells. In addition, steady state levels of GRP94 protein were decreased in established gastric cancer SGC7901 cells with knocked-down levels of ER-α36 expression and in xenograft tumours formed by these cells. Forced expression of recombinant ER-α36 in SGC7901 cells, however, up-regulated the levels of GRP94 expression.

Conclusions: Glucose-regulated protein 94 is a downstream effector of ER-α36-mediated oestrogen signalling, and may be involved in ER-α36 function during gastric carcinogenesis.

Keywords: gastric cancer; glucose-regulated protein 94; oestrogen receptor-α36; oestrogen signalling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenocarcinoma / etiology
  • Adenocarcinoma / metabolism
  • Adenocarcinoma / pathology
  • Adult
  • Aged
  • Aged, 80 and over
  • Animals
  • Blotting, Western
  • Carcinogenesis
  • Cell Line, Tumor
  • Estrogen Receptor alpha / antagonists & inhibitors
  • Estrogen Receptor alpha / genetics
  • Estrogen Receptor alpha / metabolism*
  • Female
  • Gene Knockdown Techniques
  • Heterografts
  • Humans
  • Immunohistochemistry
  • Lymphatic Metastasis
  • Male
  • Membrane Glycoproteins / metabolism*
  • Mice
  • Mice, Nude
  • Middle Aged
  • Neoplasm Staging
  • Signal Transduction
  • Stomach Neoplasms / etiology
  • Stomach Neoplasms / metabolism*
  • Stomach Neoplasms / pathology
  • Up-Regulation

Substances

  • ESR1 protein, human
  • Estrogen Receptor alpha
  • Membrane Glycoproteins
  • endoplasmin