Galectin-3 as a marker and potential therapeutic target in breast cancer

PLoS One. 2014 Sep 25;9(9):e103482. doi: 10.1371/journal.pone.0103482. eCollection 2014.

Abstract

Galectin-3 has a relatively high level of expression in triple-negative breast cancers and is a potential marker for this disease. However, the clinical and prognostic implications of galectin-3 expression in breast cancer remain unclear. We examined mastectomy specimens from 1086 breast cancer cases and matching, adjacent non-cancerous tissues using immunohistochemistry. Overall, triple-negative breast cancers expressed galectin-3 more strongly than did other breast cancers types (63.59% vs 21.36%, P = 0.001). Galectin-3 expression was not found to be an independent prognostic factor for breast cancer by Cox regression analysis, but was associated with chemotherapeutic resistance. Apoptosis was only weakly induced by arsenic trioxide (ATO) treatment in galectin-3-positive breast cancer cells (MDA-MB-231 and MCF-7), although ATO treatment up-regulated galectin-3 expression. Knockdown of galectin-3 in MDA-MB-231 cells sensitized them to killing by ATO. These findings support a possible role for galectin-3 as a marker for triple-negative breast cancer progression and as a therapeutic target in combination with ATO treatment, although the mechanisms that underlie this synergy require further investigation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Apoptosis / drug effects
  • Arsenic Trioxide
  • Arsenicals / pharmacology
  • Biomarkers, Tumor / deficiency
  • Biomarkers, Tumor / genetics
  • Biomarkers, Tumor / metabolism*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / pathology
  • Cell Line, Tumor
  • Drug Resistance, Neoplasm
  • Female
  • Galectin 3 / deficiency
  • Galectin 3 / genetics
  • Galectin 3 / metabolism*
  • Gene Expression Regulation, Neoplastic / drug effects
  • Gene Knockdown Techniques
  • Humans
  • Molecular Targeted Therapy*
  • Oxides / pharmacology
  • RNA, Small Interfering / genetics
  • Survival Analysis

Substances

  • Arsenicals
  • Biomarkers, Tumor
  • Galectin 3
  • Oxides
  • RNA, Small Interfering
  • Arsenic Trioxide

Grants and funding

This study was funded by the China National Natural Science Foundation (No. 81102029 and 81172047) and Liaoning National Natural Science Foundation (No. 2013021006). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.