Prognostic Value of GPNMB, EGFR, p-PI3K, and Ki-67 in Patients with Esophageal Squamous Cell Carcinoma

Anal Cell Pathol (Amst). 2022 Aug 31:2022:9303081. doi: 10.1155/2022/9303081. eCollection 2022.

Abstract

Background: GPNMB is a newly discovered tumour-promoting factor that may promote tumour cell progression by activating the PI3K/AKT pathway by EGFR. However, there are insufficient studies about GPNMB in ESCC. This study investigated the relationship between GPNMB and EGFR/PI3K pathway genes in ESCC.

Methods: The expression levels of GPNMB, EGFR, p-PI3K, and Ki-67 were examined using immunohistochemistry. Statistical analysis was done by SPSS 22.0 and R.

Results: GPNMB mRNA expression is higher in ESCC compared with paracancerous tissues. The expression of EGFR, PIK3CA, PIK3CB, and AKT1 was increased in GPNMB upregulated samples. GPNMB expression was positively correlated with EGFR, p-PI3K, and Ki-67 expression. GPNMB was expressed higher in the AJCC III stage, lymph node metastasis, and moderately poorly differentiated patients. EGFR was higher expressed in patients with vascular invasion; p-PI3K expression in Kazak was higher than that in Han; Ki-67 expression was higher in tumour size ≥ 3 cm. Patients with high expression of GPNMB, p-PI3K, and Ki-67 had worse OS. p-PI3K, Ki-67, nerve invasion, and lymphatic metastasis were independent risk factors, and postoperative adjuvant therapy was a protective factor in ESCC.

Conclusion: As a tumour-promoting factor, GPNMB is expected to be a potential target for ESCC.

MeSH terms

  • Carcinoma, Squamous Cell* / metabolism
  • Class I Phosphatidylinositol 3-Kinases
  • ErbB Receptors / genetics
  • ErbB Receptors / metabolism
  • Esophageal Neoplasms* / pathology
  • Esophageal Squamous Cell Carcinoma*
  • Humans
  • Ki-67 Antigen
  • Lymphatic Metastasis
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Phosphatidylinositol 3-Kinases / metabolism
  • Prognosis

Substances

  • GPNMB protein, human
  • Ki-67 Antigen
  • Membrane Glycoproteins
  • Class I Phosphatidylinositol 3-Kinases
  • EGFR protein, human
  • ErbB Receptors