Targeting Tumor Hypoxia: Suppression of Breast Tumor Growth and Metastasis by Novel Carbonic Anhydrase IX Inhibitors

Yuanmei Lou(École Nationale Supérieure de Chimie de Montpellier), Paul C. McDonald(École Nationale Supérieure de Chimie de Montpellier), Arusha Oloumi(École Nationale Supérieure de Chimie de Montpellier), Stephen Chia(École Nationale Supérieure de Chimie de Montpellier), Christina Ostlund(École Nationale Supérieure de Chimie de Montpellier), Ardalan Ahmadi(École Nationale Supérieure de Chimie de Montpellier), Alastair H. Kyle(École Nationale Supérieure de Chimie de Montpellier), Ulrich auf dem Keller(École Nationale Supérieure de Chimie de Montpellier), Samuel Leung(École Nationale Supérieure de Chimie de Montpellier), David Huntsman(École Nationale Supérieure de Chimie de Montpellier), Blaise Clarke(École Nationale Supérieure de Chimie de Montpellier), Brent W. Sutherland(École Nationale Supérieure de Chimie de Montpellier), Dawn Waterhouse(École Nationale Supérieure de Chimie de Montpellier), Marcel B. Bally(École Nationale Supérieure de Chimie de Montpellier), Calvin D. Roskelley(École Nationale Supérieure de Chimie de Montpellier), Christopher M. Overall(École Nationale Supérieure de Chimie de Montpellier), Andrew I. Minchinton(École Nationale Supérieure de Chimie de Montpellier), Fabio Pacchiano(École Nationale Supérieure de Chimie de Montpellier), Fabrizio Carta(École Nationale Supérieure de Chimie de Montpellier), Andrea Scozzafava(École Nationale Supérieure de Chimie de Montpellier), Nadia Touisni(École Nationale Supérieure de Chimie de Montpellier), Jean‐Yves Winum(École Nationale Supérieure de Chimie de Montpellier), Claudiu T. Supuran(École Nationale Supérieure de Chimie de Montpellier), Shoukat Dedhar(École Nationale Supérieure de Chimie de Montpellier)
Cancer Research
March 17, 2011
Cited by 754

Abstract

Carbonic anhydrase IX (CAIX) is a hypoxia and HIF-1-inducible protein that regulates intra- and extracellular pH under hypoxic conditions and promotes tumor cell survival and invasion in hypoxic microenvironments. Interrogation of 3,630 human breast cancers provided definitive evidence of CAIX as an independent poor prognostic biomarker for distant metastases and survival. shRNA-mediated depletion of CAIX expression in 4T1 mouse metastatic breast cancer cells capable of inducing CAIX in hypoxia resulted in regression of orthotopic mammary tumors and inhibition of spontaneous lung metastasis formation. Stable depletion of CAIX in MDA-MB-231 human breast cancer xenografts also resulted in attenuation of primary tumor growth. CAIX depletion in the 4T1 cells led to caspase-independent cell death and reversal of extracellular acidosis under hypoxic conditions in vitro. Treatment of mice harboring CAIX-positive 4T1 mammary tumors with novel CAIX-specific small molecule inhibitors that mimicked the effects of CAIX depletion in vitro resulted in significant inhibition of tumor growth and metastasis formation in both spontaneous and experimental models of metastasis, without inhibitory effects on CAIX-negative tumors. Similar inhibitory effects on primary tumor growth were observed in mice harboring orthotopic tumors comprised of lung metatstatic MDA-MB-231 LM2-4(Luc+) cells. Our findings show that CAIX is vital for growth and metastasis of hypoxic breast tumors and is a specific, targetable biomarker for breast cancer metastasis.


Related Papers

No related papers found

Powered by citation graph analysis