Lipid profiles for HER2-positive breast cancer

Anticancer Res. 2013 Jun;33(6):2467-72.

Abstract

Background: Accumulating data indicate that human epidermal growth factor receptor-2 (HER2)-positive breast cancer is a heterogeneous disease. We undertook a study to correlate lipid profiles with heterogeneous clinicopathological features of HER2-positive breast cancer.

Materials and methods: Histology-directed matrix-assisted laser desorption/ionization (MALDI)-mass spectrometry (MS) analyses were performed on 22 retrospective frozen tissue samples collected from patients with HER2-positive metastatic breast cancer, in order to correlate lipid profiles with clinicopathological characteristics. Additionally, a pair of tumor and adjacent normal tissue was profiled to identify cancer-associated changes in lipid profiles.

Results: Sphingomyelin 34:1, phosphatidylcholine (PC) 32:0, and PC 34:1, and PC 36:2 were overexpressed in HER2-positive breast cancer compared to adjacent normal tissue (HER2 signature). Lipid MALDI-MS profiles were different between Ki-67-high and Ki-67-low tumors. The proliferation signature (Ki-67-high vs. Ki-67-low) and the HER2 signature (cancer vs. normal) did not significantly overlap with each other.

Conclusion: For the first time to our knowledge, this study describes lipid profiles correlated with various clinicopathological characteristics of HER2-positive breast cancer. Lipid profiling might be helpful for the molecular characterization of this disease.

Keywords: HER2; MALDI; breast cancer; lipid; profiles.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers, Tumor / metabolism
  • Breast Neoplasms / metabolism*
  • Female
  • Humans
  • Ki-67 Antigen / metabolism*
  • Lipid Metabolism
  • Lipids / analysis*
  • Middle Aged
  • Phosphatidylcholines / metabolism*
  • Receptor, ErbB-2 / metabolism
  • Retrospective Studies
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
  • Sphingomyelins / metabolism*

Substances

  • Biomarkers, Tumor
  • Ki-67 Antigen
  • Lipids
  • Phosphatidylcholines
  • Sphingomyelins
  • ERBB2 protein, human
  • Receptor, ErbB-2