Elevated HMGA2 expression is associated with cancer aggressiveness and predicts poor outcome in breast cancer

Cancer Lett. 2016 Jul 1;376(2):284-92. doi: 10.1016/j.canlet.2016.04.005. Epub 2016 Apr 7.

Abstract

High mobility group AT-hook 2 (HMGA2) is involved in a wide spectrum of biological processes and is upregulated in several tumors. Here, we collected 273 breast cancer (BC) specimens as a training set and 310 specimens as a validation set to examine the expression of HMGA2 by immunohistochemical staining. It was found that HMGA2 expression was significantly positively correlated with advanced tumor grade and poor survival. Subgroup analysis indicated that high level of HMGA2 was significantly correlated with poor prognosis, especially in the subgroups of stage II-III, low pathological grade and non-triple negative breast cancer cases. Gene set enrichment analysis (GSEA) demonstrated a significant positive correlation between HMGA2 level and the gene expression signature of metaplastic and mesenchymal phenotype. Importantly, we also observed that ectopic expression of HMGA2 promoted the migration and invasion of breast cancer cells, and protected cancer cells against genotoxic stress from agents stimulating P53 (Ser15) phosphorylation. As a conclusion, expression of HMGA2 might indicate more advanced malignancy of breast cancer. Thus we believe HMGA2 could serve as a biomarker of poor prognosis and a novel target in treating BC tumors.

Keywords: Breast cancer; High mobility group AT-hook 2; Prognostic biomarker; Tumor progression.

Publication types

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

MeSH terms

  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / metabolism*
  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / mortality
  • Breast Neoplasms / pathology
  • Cell Movement*
  • Cell Proliferation
  • Female
  • Gene Expression Profiling
  • Genetic Predisposition to Disease
  • HMGA2 Protein / genetics
  • HMGA2 Protein / metabolism*
  • Humans
  • Immunohistochemistry
  • Kaplan-Meier Estimate
  • MCF-7 Cells
  • Middle Aged
  • Neoplasm Grading
  • Neoplasm Invasiveness
  • Phenotype
  • Phosphorylation
  • Predictive Value of Tests
  • Proportional Hazards Models
  • Reproducibility of Results
  • Risk Factors
  • Time Factors
  • Transfection
  • Treatment Outcome
  • Tumor Suppressor Protein p53 / metabolism
  • Up-Regulation

Substances

  • Biomarkers, Tumor
  • HMGA2 Protein
  • TP53 protein, human
  • Tumor Suppressor Protein p53