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

被引:639
作者
Lou, Yuanmei [1 ]
McDonald, Paul C. [1 ]
Oloumi, Arusha [1 ]
Chia, Stephen [2 ]
Ostlund, Christina [1 ]
Ahmadi, Ardalan [1 ]
Kyle, Alastair [1 ]
Keller, Ulrich Auf Dem [5 ]
Leung, Samuel [7 ]
Huntsman, David [3 ,7 ]
Clarke, Blaise [7 ,8 ]
Sutherland, Brent W. [4 ]
Waterhouse, Dawn [4 ]
Bally, Marcel [4 ]
Roskelley, Calvin [6 ]
Overall, Christopher M. [5 ]
Minchinton, Andrew [1 ]
Pacchiano, Fabio [9 ]
Carta, Fabrizio [9 ]
Scozzafava, Andrea [9 ]
Touisni, Nadia [10 ]
Winum, Jean-Yves [10 ]
Supuran, Claudiu T. [9 ]
Dedhar, Shoukat [1 ,5 ]
机构
[1] British Columbia Canc Res Ctr, Dept Integrat Oncol, Vancouver, BC V5Z 1L3, Canada
[2] British Columbia Canc Res Ctr, Dept Med Oncol, Vancouver, BC V5Z 1L3, Canada
[3] British Columbia Canc Res Ctr, Ctr Translat & Appl Genom, Vancouver, BC V5Z 1L3, Canada
[4] British Columbia Canc Res Ctr, Dept Expt Therapeut, Vancouver, BC V5Z 1L3, Canada
[5] Univ British Columbia, Dept Biochem & Mol Biol, Vancouver, BC V5Z 1M9, Canada
[6] Univ British Columbia, Dept Cell & Physiol Sci, Vancouver, BC V5Z 1M9, Canada
[7] Genet Pathol Evaluat Ctr, Vancouver, BC, Canada
[8] Toronto Gen Hosp, Dept Pathol, Toronto, ON, Canada
[9] Univ Florence, Lab Chim Bioinorgan, I-50121 Florence, Italy
[10] Univ Montpellier 1 & 2, CNRS, UMR 5247, Inst Biomol Max Mousseron,Ecol Natl Super Chim Mo, F-34296 Montpellier, France
基金
加拿大健康研究院;
关键词
MONOCLONAL-ANTIBODY; INTRACELLULAR PH; POOR-PROGNOSIS; CANCER-CELLS; ISOZYME-IX; EXPRESSION; SURVIVAL; MARKER; DISSEMINATION; MECHANISMS;
D O I
10.1158/0008-5472.CAN-10-4261
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. Cancer Res; 71(9); 3364-76. (C) 2011 AACR.
引用
收藏
页码:3364 / 3376
页数:13
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