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Prognostic relevance of carbonic anhydrase IX expression is distinct in various subtypes of breast cancer and its silencing suppresses self-renewal capacity of breast cancer cells

  • La¯sma Ivanova
  • , Eli¯na Zandberga
  • , Kari¯na Silin¸a
  • , Zane Kalnin¸a
  • , Artu¯rs A¯bols
  • , Edgars Endzelin¸š
  • , Ineta Vendina
  • , Nadezhda Romanchikova
  • , Alinta Hegmane
  • , Pe¯teris Trapencieris
  • , Ja¯nis Egli¯tis
  • , Aija Line¯*
  • *Corresponding author for this work
  • Latvian Institute of Organic Synthesis
  • Riga East University Hospital
  • University of Latvia

Research output: Contribution to journal › Article › peer-review

49 Citations (Scopus)

Abstract

Purpose: Carbonic anhydrase IX (CAIX) is a hypoxia-inducible enzyme with extracellular catalytic domain that is overexpressed in a variety of cancers including breast cancer and plays a crucial role in maintaining favourable intracellular pH and reducing extracellular pH. The purpose of the current study was to elucidate the prognostic significance of CAIX in the intrinsic subtypes of breast cancer and to characterise CAIX as a drug target in breast cancer. Methods: The prognostic significance of CAIX mRNA expression was interrogated in a cohort of 3,455 breast tumours by using an online tool, Kaplan-Meier plotter. The functional effects of stable CAIX depletion by shRNA in three breast cancer cell lines - MDA-MB-231, MCF7 and SKBR-3, representing basal-like, luminal A and HER2+ subtypes, respectively - were studied by proliferation, invasion, clonal spheroid formation and chemosensitivity assays under normoxia and hypoxia. Finally, the effect of pharmacological CA inhibition alone or in the combination with doxorubicin on self-renewal was assessed by spheroid-forming assay. Results: High CAIX mRNA expression was significantly associated with poor survival in patients with basal-like, luminal B and triple-negative breast cancer, but not luminal A and HER+ subtypes. Silencing of CAIX expression had no significant effect on the cell proliferation or viability upon treatment with doxorubicin in any of the cell lines studied, while it inhibited spheroid formation in hypoxic conditions. Furthermore, pharmacological inhibition of CAs using acetazolamide had a synergistic effect with doxorubicin on decreasing the spheroid-forming efficiency in MDA-MB-231 cells. Conclusions: Inhibition of CAIX reduces the self-renewal capacity of breast cancer cells, and the combination of doxorubicin and CAIX inhibition is an attractive therapeutic strategy in basal-like and triple-negative breast cancer, which warrants further investigations.

Original languageEnglish
Pages (from-to)235-246
Number of pages12
JournalCancer Chemotherapy and Pharmacology
Volume75
Issue number2
DOIs
Publication statusPublished - Feb 2015

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Breast cancer
  • Carbonic anhydrase IX
  • Hypoxia
  • Self-renewal
  • Spheroid-forming assay

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