Disease Markers

Disease Markers / 2016 / Article

Research Article | Open Access

Volume 2016 |Article ID 9810383 | https://doi.org/10.1155/2016/9810383

Ursa Brown-Glaberman, Marilyn Marron, Pavani Chalasani, Robert Livingston, Maria Iannone, Jennifer Specht, Alison T. Stopeck, "Circulating Carbonic Anhydrase IX and Antiangiogenic Therapy in Breast Cancer", Disease Markers, vol. 2016, Article ID 9810383, 7 pages, 2016. https://doi.org/10.1155/2016/9810383

Circulating Carbonic Anhydrase IX and Antiangiogenic Therapy in Breast Cancer

Academic Editor: Ralf Lichtinghagen
Received04 Aug 2015
Accepted29 Dec 2015
Published28 Jan 2016


Introduction. Carbonic anhydrase IX (CAIX) is a hypoxia regulated metalloenzyme integral to maintaining cellular pH. Increased CAIX expression is associated with poor prognosis in breast cancer. To explore CAIX as a biomarker for breast cancer therapies, we measured plasma CAIX levels in healthy control subjects and in breast cancer patients. Methods. In control subjects we evaluated plasma CAIX stability via commercially available ELISA. We then similarly quantified plasma CAIX levels in (1) locally advanced breast cancer (LABC) patients treated with neoadjuvant paclitaxel + sunitinib (T + S) followed by doxorubicin and cyclophosphamide (AC); (2) metastatic breast cancer (MBC) patients treated with systemic chemotherapy. Results. Plasma CAIX levels were stable at room temperature for at least 48 hours in control subjects. Mean baseline plasma CAIX levels were lower in controls compared to patients with LABC or MBC. In LABC, CAIX levels rose significantly in response to administration of antiangiogenic therapy (T + S) () but not AC (). In patients with MBC treated without an antiangiogenic agent CAIX levels did not change with therapy. Conclusions. Our results suggest that CAIX may be an easily obtained, stable measure of tumor associated hypoxia as well as a useful pharmacodynamic biomarker for antiangiogenic therapy.

1. Introduction

Carbonic anhydrase IX (CAIX), one of the 15 carbonic anhydrase (CA) isoforms found in humans, is a membranous metalloenzyme that facilitates the reversible hydration of carbon dioxide to bicarbonate and protons [1]. CAIX is regulated by hypoxia inducible factor-1 alpha (HIF-1α) and is essential for the elimination of acid loads generated by glycolysis. Thus, CAIX plays a major role in maintaining the pH gradient between cells and their extracellular space [2]. An emerging hallmark of cancer is aberrant tumor metabolism, typically characterized by a reliance on glycolysis rather than oxidative phosphorylation [3]. The increased quantities of lactate generated by this aberrant metabolism force tumor cells to acquire adaptive mechanisms to avoid excessive acidosis and perturbations in intracellular pH (pHi). CAs are integral to this process by facilitating proton export and bicarbonate recycling. CAIX is unique among the CA isoforms in that it is seldom expressed in normal tissue and is directly linked to cellular hypoxia, with tumoral expression restricted to perinecrotic or hypoxic regions [1].

Carbonic anhydrase IX, previously referred to as the membrane antigen MN or G250MN, was originally identified in HeLa cells [4]. CAIX mRNA is expressed in >95% of clear cell renal cell carcinomas (ccRCC) [5]. ccRCC is unique among the solid tumors in that HIF-1α activity and in turn CAIX expression are no longer tied directly to hypoxia but rather to loss of functional Von Hippel Lindau (VHL) protein. This is thought to explain the near ubiquitous expression of CAIX in ccRCC [6]. Multiple studies have evaluated the prognostic significance of tissue CAIX expression in ccRCC with the majority suggesting that low CAIX expression is associated with worse outcomes [7]. Stewart et al. evaluated CAIX protein expression in ccRCC tumors before and after exposure to vascular endothelial growth factor- (VEGF-) targeted tyrosine kinase inhibitor (TKI) therapy (sunitinib or pazopanib) [8]. They demonstrated that tissue CAIX expression rose following VEGF-targeted therapy and that those patients with high tissue CAIX expression after therapy had improved outcomes, suggesting that CAIX may be a predictive biomarker for antiangiogenic therapy [8].

Carbonic anhydrase IX expression has similarly been confirmed by immunohistochemistry (IHC) in other solid tumor types, including breast cancer [9, 10]. Unlike in ccRCC, high CAIX tumor expression has been associated with poor prognosis and chemoresistance in multiple cancer types, including cervical, lung, head and neck, and breast cancer [1013].

Recognition that CAIX was shed from propagated cancer cells into culture media led to interest in evaluating CAIX levels in the serum and urine of cancer patients. Závada et al. first described increased expression of the soluble, extracellular CAIX domain in the serum and urine of 50 patients with renal cell carcinoma [14]. In this paper, we describe measurement of circulating plasma CAIX in healthy controls and report its utility as a potential biomarker for antiangiogenic therapy in breast cancer patients.

2. Patients and Controls

To determine CAIX stability in plasma, we evaluated CAIX levels in ten healthy control subjects (five female and five male patients, age range 26–67 years) at time 0 and then 6 months later. We then quantified plasma CAIX levels from two breast cancer patient cohorts treated on chemotherapeutic trials. The first cohort consisted of 57 women with HER2 negative locally advanced or inflammatory breast cancer (LABC) treated in the neoadjuvant setting with paclitaxel in combination with the antiangiogenic VEGF-targeted TKI, sunitinib, for 12 weeks followed by continuous anthracycline/cyclophosphamide (AC, weekly doxorubicin and daily oral cyclophosphamide with granulocyte colony-stimulating factor support) for 15 weeks (patient population further described in [15]). Plasma was collected at baseline, after completion of paclitaxel plus sunitinib (T + S) therapy, and at the completion of AC prior to surgery. The second patient cohort consisted of 23 women treated for metastatic breast cancer (MBC) with either irinotecan + etoposide or weekly paclitaxel + a novel immunomodulatory agent. The metastatic patient population was heterogeneous with regard to hormone receptor and HER2 status, as well as number of prior lines of therapy. Plasma samples were collected at baseline and following 4–6 weeks of systemic chemotherapy.

3. Methods

For all samples, plasma CAIX was quantified using an enzyme-linked immunosorbent assay (ELISA) kit (Quantikine Human Carbonic Anhydrase IX/CA9 Immunoassay, R&D Systems). Plasma CAIX was quantified in duplicate for control subjects and in triplicate for breast cancer patients. Blood from control subjects was collected with heparin and acid citrate dextrose (ACD) as anticoagulant and analyzed at preplanned time points (within 1 hour, 24 hours, and 48 hours after phlebotomy). For breast cancer patients, plasma was collected in ACD (LABC and subset MBC) or in heparin (subset MCB) and stored at −80°C for batch analysis.

Plasma CAIX mean, median, and range were determined for each group and at each time point. Differences in CAIX levels between baseline and follow-up were compared and statistical significance was determined by paired -test or one-way ANOVA analysis with values ≤0.05 considered significant. In the LABC and MBC groups, patients were divided by the median baseline plasma CAIX level into low and high groups. The median level was chosen as the cut-point as it provides the most power assuming a continuous effect across the spectrum of values, for ease of interpretation and to avoid testing multiple cut-points.

4. Results

4.1. Healthy Control Subjects

In the healthy control subjects, we first evaluated the effect of heparin versus ACD anticoagulant on plasma CAIX levels. Subsequently, we evaluated the plasma stability of CAIX by quantifying levels within 1 hour as well as at 24 and 48 hours after phlebotomy (Table 1). Intrapatient plasma CAIX levels from blood anticoagulated with ACD were highly correlated with levels from blood anticoagulated with heparin (). However, CAIX levels were on average slightly higher (4.6 pg/mL) in blood anticoagulated with heparin compared to ACD (). No significant differences were observed in CAIX levels obtained from plasma collected, spun, and aliquoted within 1 hr after phlebotomy compared to plasma assayed after the blood had remained at room temperature for 24 and 48 hours prior to being spun, aliquoted, and frozen down (heparin , ACD ). Plasma CAIX levels were also remeasured at six months in five of the control subjects (ACD only) with no differences observed in the repeat measurements (). While there was a trend toward higher CAIX levels in females when compared to males (mean level 26.2 versus 14.9 pg/mL), this difference was not statistically significant ().

Timing plasma collectionAnticoagulant#CAIX, pg/mL
MeanMedian Range

Baseline, within 1 hr after phlebotomy ACD20.517.48.8–41.2
Baseline, 24 hrs after phlebotomy ACD21.116.48.7–36.4
Baseline, 48 hrs after phlebotomy ACD20.316.78.6–36.8
6-month follow-up, within 1 hr after phlebotomyACD22.4826.99.5–28.0
Baseline, within 1 hr after phlebotomy Heparin–45.9
Baseline, 24 hrs after phlebotomy Heparin 24.921.211.1–46.1
Baseline, 48 hrs after phlebotomy Heparin 26.222.710.8–50.2

Referring to the time blood remained at room temperature prior to plasma separation, aliquoting, and freezing. #CAIX levels were on average 4.6 pg/mL higher in blood anticoagulated with heparin compared to ACD (). ACD: acid citrate dextrose; hr: hour; hrs: hours.
4.2. Breast Cancer Patients

In patients with breast cancer, plasma CAIX levels were evaluated at baseline as well as longitudinally in response to the administration of antitumor therapies. In patients with LABC as well as MBC, a wide range of baseline CAIX levels was observed (Table 2). Patients with MBC had significantly higher baseline CAIX levels (mean 90.7 pg/mL) compared to patients with LABC (mean 34.0 pg/mL) or healthy controls (mean 20.5 pg/mL) (Figure 1).

Patient populationChemotherapyTime pointsCAIX, pg/mL
MeanMedian Range

LABCNeoadjuvant paclitaxel (T) + sunitinib (S) × 12 weeks followed by anthracycline (AC) × 15 weeksBaseline () 34.026.00–155
Following T + S ()48.428.50–239
Following AC () 49.642.215–172

MBCIrinotecan + etoposide or paclitaxel + immunomodulatory agent Baseline ()90.776.931.2–254.7
Following 4–6 weeks of90.774.327.2–224
chemotherapy ()

LABC: locally advanced breast cancer; MBC: metastatic breast cancer.

In patients with LABC, CAIX levels rose significantly in response to the administration of paclitaxel plus sunitinib () but not to anthracycline based therapy () (Figure 2(b)). The rise in CAIX in response to paclitaxel plus sunitinib was statistically significant only in patients with lower baseline CAIX levels () (Figure 2(a)). In patients with MBC treated with cytotoxic chemotherapies (without an antiangiogenic agent), CAIX levels did not change in response to therapy administration (Figure 3).

In patients with LABC, elevated baseline plasma CAIX levels were also associated with triple negative histology and a decreased clinical/pathologic response to neoadjuvant chemotherapy. Patients with a baseline CAIX level below the median had a complete pathologic response (pCR) rate of 44.8% at the time of surgery compared to a pCR rate of 11.5% in those with a baseline CAIX level greater or equal to the median value () (manuscript in preparation; see [16]).

5. Discussion

Biomarkers for response to antiangiogenic therapy remain elusive despite the extensive use of antiangiogenic therapies in cancer patients and the intense search for predictive markers. Circulating plasma CAIX has several attributes suggesting it may be a promising biomarker for antiangiogenic therapies in breast cancer. First, it is exclusively regulated by HIF-1 alpha and thus increases rapidly in response to tissue sensed hypoxia. CAIX is also crucial for maintaining the cellular pH in tumor cells that have switched to a glycolytic phenotype and thus a marker for tumor cells that have already adapted to a hypoxic, acidotic environment.

In this paper, we extended the findings of Wind et al. who previously evaluated two commercially available ELISA kits for measuring circulating CAIX and found that the R&D Systems kit was suitable for use with both serum and plasma collected from blood anticoagulated with EDTA with reliable, reproducible results [17]. We have also shown that CAIX levels are stable for at least 48 hours after phlebotomy, assessable in plasma anticoagulated with either ACD or heparin, and remarkably stable over time.

Elevated tissue and circulating CAIX levels have been associated with a more aggressive phenotype, resistance to chemotherapy, and poor prognosis in breast cancer. Chia et al. initially characterized CAIX expression in primary breast tumors from 103 women [10]. CAIX expression was detectable in 48% of cases as strong membranous staining within epithelial tumor cells. The pattern of expression was typically limited to tumor cells immediately adjacent to areas of necrosis [10]. CAIX expression was associated with the presence of tumor necrosis, higher grade, loss of estrogen receptor (ER) expression, and decreased recurrence-free and overall survival [10]. The correlation between elevated CAIX expression, aggressive histology, and poor prognosis has subsequently been confirmed in several series with the highest expression observed in basal-type breast cancers (51%) and the lowest in luminal A subtypes (8%) [1821]. High tumor CAIX expression may also correlate with resistance to chemotherapy as patients with early stage basal-like breast cancer positive for CAIX expression had significantly shorter survival when compared to patients with CAIX-negative basal-like breast cancer () [22]. Similarly, breast tumors that expressed higher levels of CAIX had lower pathologic complete response (pCR) rates when treated with neoadjuvant anthracycline/taxane based therapy [23].

There are multiple hypotheses that may explain the association between high CAIX expression and poor outcome in breast cancer. CAIX expression is closely linked to tissue hypoxia and acidosis suggesting that its upregulation is part of the tumor’s adaptation to survive and even thrive under hypoxic conditions, including those generated by antiangiogenic therapies [19]. Tumors that develop a glycolytic-acid resistant phenotype require upregulation of CAIX to maintain their intracellular pH while fostering acidification of the extracellular space. This acidity contributes to breakdown of the extracellular matrix increasing the tumor’s invasive potential [19, 24]. Increased intratumoral hypoxia may also contribute to genomic instability and the loss of genomic integrity [25] as elevated CAIX expression has been associated with loss of BRCA1 function [26, 27]. CAIX has also been proposed to influence the expansion and survival of breast cancer stem cells under hypoxic conditions [28].

The clinical significance of circulating CAIX levels in patients with metastatic and early stage breast cancer has been previously reported [24, 29]. Müller et al. prospectively examined serum CAIX levels from a heterogeneous group of 253 patients with metastatic breast cancer [24]. Patients with elevated CAIX levels (35% of patients) had a significantly worse median progression-free survival (PFS) and overall survival (OS) (). On multivariate analysis with established prognostic factors, the presence of circulating tumor cells, the line of therapy, and elevated serum CAIX remained independent predictors of OS [24].

Schütze et al. similarly evaluated serum CAIX and tumor CAIX expression by microarray analysis in patients with stage I–III breast cancer [29]. In the 76 patients with both tissue CAIX RNA and serum CAIX levels, there was no correlation between serum levels and tumor RNA expression () or between CAIX and overall survival. The authors suggested this seemingly contradictory result may be related to differences in treatment after recurrence, the relatively small size of the patient cohort, and the different techniques used for tissue CAIX analyses (tissue RNA as opposed to IHC). However, neither study examined changes in circulating CAIX in response to chemotherapy.

Our work in breast cancer patients further expands on these results and provides additional patient data showing that plasma CAIX levels are elevated in patients with MBC when compared to those with LABC or to healthy controls and that elevated CAIX levels may predict tumors adapted to a glycolytic, acidic, and hypoxic environment. In addition, our results show that changes in circulating CAIX levels are observed in response to the administration of antiangiogenic but not cytotoxic chemotherapy. Further work is needed to explore the relationship between circulating CAIX levels and clinical outcome in patients with breast cancer.

The wide range in baseline CAIX levels in patients with MBC and LABC may in part explain the varied response historically observed with therapies targeting angiogenesis. Those tumors adapted to a hypoxic/acidotic environment, as suggested by elevated baseline CAIX levels, may be less sensitive to such therapies as they have developed compensatory mechanisms to survive in devascularized conditions. Supporting this hypothesis, Shan et al. demonstrated that elevated tissue CAIX expression in primary breast cancer is associated with lower tumor microvessel density and increased tumor necrosis [30]. Additionally, knock-down of CAIX expression in colon cancer cell lines was found to enhance the effects of bevacizumab treatment, perhaps by preventing tumors from adapting to the increased hypoxia induced by anti-VEGF treatment [31].

Multiple selective CAIX inhibitors are currently under evaluation in the preclinical setting [32, 33]. SLC-0111 is an orally bioavailable, highly selective small molecule inhibitor of CAIX and CAXII. Daily oral administration of SLC-0111 to mice harboring MDA-MB-231 LM2-4 orthotopic human breast tumors (known to be ER/PR and HER2 negative, CAIX-positive) resulted in significant, dose-dependent reductions in tumor growth [34]. Furthermore, treatment with SLC-0111 in combination with paclitaxel was significantly more effective at inhibiting tumor growth compared to either treatment alone, with no additional toxicity. Phase I study is currently underway investigating the safety, tolerability, and pharmacokinetics of SLC-0111 in patients with advanced solid tumors (clinicaltrials.gov, NCT02215850).

In conclusion, our results validate circulating CAIX as a robust and easily measurable biomarker of hypoxia and HIF-1α upregulation that may prove useful in identifying patients unlikely to benefit from antiangiogenic therapy. Similarly, CAIX may be a future target of interest in breast cancer with the potential of augmenting the effectiveness of antiangiogenic therapy by preventing tumors from surviving in and adapting to hypoxia.


AC:Doxorubicin plus cyclophosphamide
ACD:Acid citrate dextrose
CA:Carbonic anhydrase
CAIX:Carbonic anhydrase IX
CAXII:Carbonic anhydrase XII
ccRCC:Clear cell renal cell carcinoma
ELISA:Enzyme-linked immunosorbent assay
ER:Estrogen receptor
HIF-1α:Hypoxia inducible factor-1 alpha
LABC:Locally advanced breast cancer
MBC:Metastatic breast cancer
OS:Overall survival
pCR:Pathologic complete response
PFS:Progression-free survival
pHi:Intracellular pH
PR:Progesterone receptor
T + S:Paclitaxel plus sunitinib
TKI:Tyrosine kinase inhibitor
VEGF:Vascular endothelial growth factor
VHL:Von Hippel Lindau.

Ethical Approval

This research was approved by the Institutional Review Boards and the University of Arizona and University of Washington and was performed in accordance with the Declaration of Helsinki.

Patient and normal control subjects signed informed consent to participate. Patient subjects are heterogeneous, participating in several clinical protocols with informed consent allowing for the subsequent retrospective biomarker analysis performed here on banked serum and plasma specimens.

Conflict of Interests

The authors declare that they have no competing interests.

Authors’ Contribution

Ursa Brown-Glaberman carried out normal control subject recruitment, participated in study design, performed data analysis, and drafted the paper. Marilyn Marron and Maria Iannone collected plasma samples and performed ELISA and assisted with database management and data analysis. Pavani Chalasani, Robert Livingston, and Jennifer Specht participated in study design, data analysis, and paper preparation. Alison T. Stopeck conceived the study, oversaw its design and coordination, and helped to draft the paper. All authors read and approved the final paper.


Support for this project was provided by Pfizer, Inc., SI11, CC-IRB #6488, J. Specht (PI), and by the laboratory of A. Stopeck.


  1. S. Kaluz, M. Kaluzová, S.-Y. Liao, M. Lerman, and E. J. Stanbridge, “Transcriptional control of the tumor- and hypoxia-marker carbonic anhydrase 9: a one transcription factor (HIF-1) show?” Biochimica et Biophysica Acta (BBA)—Reviews on Cancer, vol. 1795, no. 2, pp. 162–172, 2009. View at: Publisher Site | Google Scholar
  2. C. P. S. Potter and A. L. Harris, “Diagnostic, prognostic and therapeutic implications of carbonic anhydrases in cancer,” British Journal of Cancer, vol. 89, no. 1, pp. 2–7, 2003. View at: Publisher Site | Google Scholar
  3. D. Hanahan and R. A. Weinberg, “Hallmarks of cancer: the next generation,” Cell, vol. 144, no. 5, pp. 646–674, 2011. View at: Publisher Site | Google Scholar
  4. E. Oosterwijk, D. J. Ruiter, P. J. Hoedemaeker et al., “Monoclonal antibody G 250 recognizes a determinant present in renal-cell carcinoma and absent from normal kidney,” International Journal of Cancer, vol. 38, no. 4, pp. 489–494, 1986. View at: Publisher Site | Google Scholar
  5. T. A. Bismar, F. J. Bianco, H. Zhang et al., “Quantification of G250 mRNA expression in renal epithelial neoplasms by real-time reverse transcription-PCR of dissected tissue from paraffin sections,” Pathology, vol. 35, no. 6, pp. 513–517, 2003. View at: Publisher Site | Google Scholar
  6. K. Grabmaier, M. C. A. de Weijert, G. W. Verhaegh, J. A. Schalken, and E. Oosterwijk, “Strict regulation of CAIXG250/MN by HIF-1α in clear cell renal cell carcinoma,” Oncogene, vol. 23, no. 33, pp. 5624–5631, 2004. View at: Publisher Site | Google Scholar
  7. A. B. Stillebroer, P. F. A. Mulders, O. C. Boerman, W. J. G. Oyen, and E. Oosterwijk, “Carbonic anhydrase IX in renal cell carcinoma: implications for prognosis, diagnosis, and therapy,” European Urology, vol. 58, no. 1, pp. 75–83, 2010. View at: Publisher Site | Google Scholar
  8. G. D. Stewart, F. C. O’Mahony, A. Laird et al., “Carbonic anhydrase 9 expression increases with vascular endothelial growth factor-targeted therapy and is predictive of outcome in metastatic clear cell renal cancer,” European Urology, vol. 66, no. 5, pp. 956–963, 2014. View at: Publisher Site | Google Scholar
  9. J. Saarnio, S. Parkkila, A.-K. Parkkila et al., “Immunohistochemistry of carbonic anhydrase isozyme IX (MN/CA IX) in human gut reveals polarized expression in the epithelial cells with the highest proliferative capacity,” Journal of Histochemistry and Cytochemistry, vol. 46, no. 4, pp. 497–504, 1998. View at: Publisher Site | Google Scholar
  10. S. K. Chia, C. C. Wykoff, P. H. Watson et al., “Prognostic significance of a novel hypoxia-regulated marker, carbonic anhydrase IX, in invasive breast carcinoma,” Journal of Clinical Oncology, vol. 19, no. 16, pp. 3660–3668, 2001. View at: Google Scholar
  11. S. Y. Liao, C. Brewer, J. Závada et al., “Identification of the MN antigen as a diagnostic biomarker of cervical intraepithelial squamous and glandular neoplasia and cervical carcinomas,” American Journal of Pathology, vol. 145, no. 3, pp. 598–609, 1994. View at: Google Scholar
  12. A. Giatromanolaki, M. I. Koukourakis, E. Sivridis et al., “Expression of hypoxia-inducible carbonic anhydrase-9 relates to angiogenic pathways and independently to poor outcome in non-small cell lung cancer,” Cancer Research, vol. 61, no. 21, pp. 7992–7998, 2001. View at: Google Scholar
  13. N. J. P. Beasley, C. C. Wykoff, P. H. Watson et al., “Carbonic anhydrase IX, an endogenous hypoxia marker, expression in head and neck squamous cell carcinoma and its relationship to hypoxia, necrosis, and microvessel density,” Cancer Research, vol. 61, no. 13, pp. 5262–5267, 2001. View at: Google Scholar
  14. J. Závada, Z. Závadová, M. Zat'ovičová, L. Hyršl, and I. Kawaciuk, “Soluble form of carbonic anhydrase IX (CA IX) in the serum and urine of renal carcinoma patients,” British Journal of Cancer, vol. 89, no. 6, pp. 1067–1071, 2003. View at: Publisher Site | Google Scholar
  15. J. M. Specht, B. Kurland, H. M. Linden et al., “A phase II study evaluating the safety and efficacy of sunitinib with weekly paclitaxel followed by doxorubicin and daily oral cyclophosphamide plus G-CSF as neoadjuvant chemotherapy (NC) for locally advanced (LABC) or inflammatory breast cancer (IBC),” Journal of Clinical Oncology, vol. 31, abstract 1090, 2013, ASCO Annual Meeting. View at: Google Scholar
  16. U. Brown-Glaberman, J. Specht, M. Iannone et al., “Circulating biomarkers in patients receiving neoadjuvant chemotherapy combined with sunitinib for locally advanced breast cancer,” Journal of Clinical Oncology, vol. 31, supplement, abstract 1089, 2013, Proceedings of the ASCO Annual Meeting. View at: Google Scholar
  17. T. C. Wind, M. P. Messenger, D. Thompson, P. J. Selby, and R. E. Banks, “Measuring carbonic anhydrase IX as a hypoxia biomarker: differences in concentrations in serum and plasma using a commercial enzyme-linked immunosorbent assay due to influences of metal ions,” Annals of Clinical Biochemistry, vol. 48, no. 2, pp. 112–120, 2011. View at: Publisher Site | Google Scholar
  18. Y. Lou, P. C. McDonald, A. Oloumi et al., “Targeting tumor hypoxia: suppression of breast tumor growth and metastasis by novel carbonic anhydrase IX inhibitors,” Cancer Research, vol. 71, no. 9, pp. 3364–3376, 2011. View at: Publisher Site | Google Scholar
  19. C.-L. Chen, J.-S. Chu, W.-C. Su, S.-C. Huang, and W.-Y. Lee, “Hypoxia and metabolic phenotypes during breast carcinogenesis: expression of HIF-1alpha, GLUT1, and CAIX,” Virchows Archiv, vol. 457, no. 1, pp. 53–61, 2010. View at: Publisher Site | Google Scholar
  20. D. Generali, S. B. Fox, A. Berruti et al., “Role of carbonic anhydrase IX expression in prediction of the efficacy and outcome of primary epirubicin/tamoxifen therapy for breast cancer,” Endocrine-Related Cancer, vol. 13, no. 3, pp. 921–930, 2006. View at: Publisher Site | Google Scholar
  21. S. A. Hussain, R. Ganesan, G. Reynolds et al., “Hypoxia-regulated carbonic anhydrase IX expression is associated with poor survival in patients with invasive breast cancer,” British Journal of Cancer, vol. 96, no. 1, pp. 104–109, 2007. View at: Publisher Site | Google Scholar
  22. E. Y. Tan, M. Yan, L. Campo et al., “The key hypoxia regulated gene CAIX is upregulated in basal-like breast tumours and is associated with resistance to chemotherapy,” British Journal of Cancer, vol. 100, no. 2, pp. 405–411, 2009. View at: Publisher Site | Google Scholar
  23. N. Aomatsu, M. Yashiro, S. Kashiwagi et al., “Carbonic anhydrase 9 is associated with chemosensitivity and prognosis in breast cancer patients treated with taxane and anthracycline,” BMC Cancer, vol. 14, no. 1, article 400, 2014. View at: Publisher Site | Google Scholar
  24. V. Müller, S. Riethdorf, B. Rack et al., “Prospective evaluation of serum tissue inhibitor of metalloproteinase 1 and carbonic anhydrase IX in correlation to circulating tumor cells in patients with metastatic breast cancer,” Breast Cancer Research, vol. 13, no. 4, article R71, 2011. View at: Publisher Site | Google Scholar
  25. R. S. Bindra, S. L. Gibson, A. Meng et al., “Hypoxia-induced down-regulation of BRCA1 expression by E2Fs,” Cancer Research, vol. 65, no. 24, pp. 11597–11604, 2005. View at: Publisher Site | Google Scholar
  26. V. M. Neumeister, C. A. Sullivan, R. Lindner et al., “Hypoxia-induced protein CAIX is associated with somatic loss of BRCA1 protein and pathway activity in triple negative breast cancer,” Breast Cancer Research and Treatment, vol. 136, no. 1, pp. 67–75, 2012. View at: Publisher Site | Google Scholar
  27. P. van der Groep, P. J. van Diest, Y. H. C. M. Smolders et al., “HIF-1α overexpression in ductal carcinoma in Situ of the breast in BRCA1 and BRCA2 mutation carriers,” PLoS ONE, vol. 8, no. 2, Article ID e56055, 2013. View at: Publisher Site | Google Scholar
  28. F. E. Lock, P. C. McDonald, Y. Lou et al., “Targeting carbonic anhydrase IX depletes breast cancer stem cells within the hypoxic niche,” Oncogene, vol. 32, no. 44, pp. 5210–5219, 2013. View at: Publisher Site | Google Scholar
  29. D. Schütze, K. Milde-Langosch, I. Witzel et al., “Relevance of cellular and serum carbonic anhydrase IX in primary breast cancer,” Journal of Cancer Research and Clinical Oncology, vol. 139, no. 5, pp. 747–754, 2013. View at: Publisher Site | Google Scholar
  30. X. Shan, D. Wang, J. Chen et al., “Necrosis degree displayed in computed tomography images correlated with hypoxia and angiogenesis in breast cancer,” Journal of Computer Assisted Tomography, vol. 37, no. 1, pp. 22–28, 2013. View at: Publisher Site | Google Scholar
  31. A. McIntyre, S. Patiar, S. Wigfield et al., “Carbonic anhydrase IX promotes tumor growth and necrosis in vivo and inhibition enhances anti-VEGF therapy,” Clinical Cancer Research, vol. 18, no. 11, pp. 3100–3111, 2012. View at: Publisher Site | Google Scholar
  32. C. Ward, S. P. Langdon, P. Mullen et al., “New strategies for targeting the hypoxic tumour microenvironment in breast cancer,” Cancer Treatment Reviews, vol. 39, no. 2, pp. 171–179, 2013. View at: Publisher Site | Google Scholar
  33. P. C. McDonald, J.-Y. Winum, C. T. Supuran, and S. Dedhar, “Recent developments in targeting carbonic anhydrase IX for cancer therapeutics,” Oncotarget, vol. 3, no. 1, pp. 84–97, 2012. View at: Publisher Site | Google Scholar
  34. P. C. McDonald, J. Sanghera, M. Singh et al., “Therapeutic targeting of cancer cells in the hypoxic microenvironment using an orally bioavailable small molecule inhibitor of carbonic anhydrase IX,” Cancer Research, vol. 74, abstract 841, 2014, Proceedings of the AACR Annual Meeting. View at: Publisher Site | Google Scholar

Copyright © 2016 Ursa Brown-Glaberman et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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