High co-expression of Sp1 and HER-2 is correlated with poor prognosis of gastric cancer patients

Surg Oncol. 2015 Sep;24(3):220-5. doi: 10.1016/j.suronc.2015.05.004. Epub 2015 Jun 3.

Abstract

The aim of this study was to investigate co-expression of HER-2 and Sp1 in gastric cancer (GC) so as to determine whether these two proteins may be correlated with poor prognosis of GC patients. We examined the HER-2 overexpression and amplification and expression levels of Sp1 in 227 GC patients using immune-histochemical staining and fluorescence in situ hybridization. Data on clinicopathological features and relevant prognostic factors in these patients were analyzed. Of the 227 gastric cancer samples, 11.89% were positive for HER-2 overexpression/amplification under the new scoring system, and the frequency of negative, weak positive and strong positive expression of Sp1 was 14.98%, 48.01% and 37.0% respectively. No statistically positive correlation was observed between the expression levels of HER-2 and Sp1 in GC tissues. HER-2 overexpression was closely correlated to the Lauren type, degree of differentiation, tumor size and lymph node metastasis, and Sp1 as well (P < 0.05). Overexpression of HER-2 and Sp1 predicted poor survival in univariate analysis as well as in a Cox proportional hazards model.

Keywords: Gastric cancer; HER-2; Immunohistochemistry; Prognosis; Sp1.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adult
  • Aged
  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / metabolism*
  • Female
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization, Fluorescence
  • Male
  • Middle Aged
  • Neoplasm Recurrence, Local / metabolism*
  • Neoplasm Staging
  • Prognosis
  • Receptor, ErbB-2 / genetics
  • Receptor, ErbB-2 / metabolism*
  • Retrospective Studies
  • Sp1 Transcription Factor / metabolism*
  • Stomach Neoplasms / diagnosis
  • Stomach Neoplasms / metabolism*
  • Survival Rate
  • Young Adult

Substances

  • Biomarkers, Tumor
  • Sp1 Transcription Factor
  • SP1 protein, human
  • ERBB2 protein, human
  • Receptor, ErbB-2