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Blood Oxygenation Level-dependent Magnetic Resonance Imaging of Breast Cancer: Correlation with Carbonic Anhydrase IX and Vascular Endothelial Growth Factor.

Byline: Ying. Wang, Min. Liu, Mu-Lan. Jin

Background: Blood oxygenation level-dependent magnetic resonance imaging (BOLD-MRI) is a functional MRI technique which involves using the paramagnetic properties of deoxyhemoglobin to image the local tissue oxygen concentration. The purpose of this study was to investigate whether BOLD-MRI could evaluate hypoxia and angiogenesis of breast invasive ductal carcinoma (IDC). Methods: Ninety-eight female patients with IDC were retrospectively included in this research. All patients underwent breast BOLD-MRI at 3.0 T before surgery. R2* values of BOLD-MRI were measured. The expression of carbonic anhydrase IX (CA IX) and vascular endothelial growth factor (VEGF) was analyzed by immunohistochemistry. Spearman's correlation analysis was used to correlate R2* value with CA IX and VEGF levels. Results: Heterogeneous intensity on BOLD-MRI images was the main finding of IDCs. The mean R2* value was 52.8 [+ or -] 18.6 Hz. The R2* values in patients with axillary lymph node metastasis were significantly higher than the R2* values in patients without axillary lymph node metastasis (t = 2.882, P= 0.005). R2* values increased with CA IX level and positively correlated with the level of CA IX (r = 0.616, P< 0.001); however, R2* value had no significantly correlation with the level of VEGF (r = 0.110, P= 0.281). Conclusion: BOLD-MRI could noninvasively evaluate chronic hypoxia of IDC, but not angiogenesis.

Introduction

Hypoxia and angiogenesis are the basic characters of breast cancer. Angiogenesis can induce capillary growth into the tumor which supplies required nutrients, leading to tumor expansion and metastases. The essential role of angiogenesis in tumor growth was first proposed by Judah Folkman, who described tumors as “hot and bloody.[sup][1]” Hypoxic tumor tissue may cause resistance to radiation therapy and some forms of chemotherapy and has been shown to be associated with malignant progression, increased incidence of metastases, and poor prognosis.[sup][2] Evaluation of hypoxia and angiogenesis in tumor will benefit most to hypoxia-modifying and anti-angiogenesis treatments.

Carbonic anhydrase IX (CA IX) is a membranously located metalloenzyme involved in pH homeostasis with the influence on regulation of cell proliferation, oncogenesis, and tumor progression. CA IX is an indicator of hypoxia in the tumor and its expression is associated with more aggressive forms of breast cancer.[sup][3],[4] Vascular endothelial growth factor (VEGF) has been demonstrated to be a major contributor to angiogenesis.[sup][5] VEGF-targeting therapies have shown significant benefits and been successfully integrated in routine clinical practice for other types of cancer. CA IX and VEGF have been used as biomarker of hypoxia and angiogenesis. Currently, magnetic resonance imaging (MRI) is the best modality for assessing morphology and function of tumor.[sup][6] Dynamic contrast-enhanced MRI (DCE-MRI) has been used to detection of angiogenesis and hypoxia of cancer and requires intravenous injection of an exogenous contrast agent such as gadolinium.[sup][7],[8] Blood oxygenation level-dependent (BOLD) MRI, first described by Ogawa and Lee,[sup][9] is a functional MRI technique which involves using the paramagnetic properties of deoxyhemoglobin to image the local tissue oxygen concentration.[sup][10],[11] BOLD-MRI contrast is sensitive to pO[sub]2 in tissues adjacent to perfused vessels, so we speculate that BOLD-MRI could noninvasively evaluate hypoxia and angiogenesis. The aim of this study was to investigate whether BOLD-MRI correlates with CA IX and VEGF in breast invasive ductal carcinoma (IDC).

Methods

Patients' selection

This study has been approved Ethics Committee of Beijing Chaoyang Hospital. Informed consent of each patient has been obtained, and the investigations have been conducted according to the Declaration of Helsinki . From January 2013 to July 2015, 98 women with breast IDCs were retrospectively included in this research. Breast MRI was obtained in all patients within one week before surgery. All included patients had no previous excisional biopsy or chemotherapy before MRI. Patients who did not undergo BOLD-MRI before surgery or were older than 75 years were excluded. The clinical information including patients' age and body mass index (BMI), tumor sizes, histological grade, and axillary lymph node metastases was referenced to the medical records.

Magnetic resonance imaging protocol

Breast MRI was performed at a 3.0 T clinical MRI system (Trio Tim, Siemens, Erlangen, Germany) using the phased array breast surface coil in the prone position. The MRI images were performed using the following sequences: The axial T2-weighted turbo spin-echo sequences and T1-weighted fast low-angle shot gradient-echo sequences, then the axial BOLD-MRI with a multiple gradient-recalled-echo sequence with repetition time/echo time of 124 ms/3.31–39.05 ms, 10 echo train length, field of view = 280 mm, matrix size = 256 mm x 256 mm, flip angle = 15[degrees], voxel size = 1.5 mm x 1.1 mm x 5.0 mm, average = 4, slice thickness = 5.0 mm with a 1-mm slice gap, voxel size = 1.5 mm x 1.1 mm x 4.0 mm, and bandwidth = 260 Hz per pixel.

Magnetic resonance imaging evaluation

After imaging, breast BOLD-MR images were transferred to AW4.4 workstation (GE Healthcare, USA). R2* values of BOLD were analyzed using a FuncTool-R2 Star software (Advantage Workstation 4.4 GE Healthcare, Milwaukee, WI, USA). One radiologist with 10-year experience in breast MRI analyzed R2* value without knowing other clinical information. A region of interest with an area of 10 [+ or -] 4 mm [sup]2 was placed in the lesions. To eliminate bias, the cystic or necrotic portions of the tumor causing T2 shine-through effect, shown as high-signal intensity on T2-weighted image, were excluded. The three measurements were averaged and used as the R2* values.

Immunohistochemistry

Immunohistochemical staining of CA IX and VEGF was, respectively, performed on 5 [micro]m formalin-fixed, paraffin-embedded tissue sections. Antigen retrieval with Tris-EDTA (pH 9.0) in a pressure cooker was performed at 95[degrees]C for 3 min. Five percent hydrogen peroxide was used for 10 min to block the endogenous peroxidase. After blocking with 2% normal horse serum for 30 min, the sections were incubated with a rabbit polyclonal antibody anti-CA IX (Abcam, Cambridge, UK, 1:1000 dilution) or a rabbit polyclonal antibody anti-VEGF (Abcam, Cambridge, UK; 1:400 dilution) for 90 min at room temperature. And biotin/avidin system using the VECTASTAIN Elite ABC kit (Vector Laboratories, California, USA) was used for this immunoperoxidase procedure. Finally, diaminobenzidine tetrahydrochloride solution (Vector Laboratories, California, USA) was used as a substrate. According to the manufacturer's recommendations, nuclei were counterstained with hematoxylin. Known positive tissue specimens were used as positive controls for CA IX and VEGF (lung cancer). Negative control slides without primary antibodies were included for each staining. Scoring was performed by an expert with 11-year experience with breast disease who was blinded to other clinical information. The staining for CA IX and VEGF was scored in a semi-quantitative method [sup][12] by estimating the percentage area of tumor cells that had been stained: negative for <1%, weakly positive for 1–10%, moderately positive for 10–50%, and strong positive for >50% immunostaining.

Statistical analysis

Analyses were performed using SPSS 13.0 statistical software (SPSS Inc., Chicago, IL, USA). All data are expressed as means [+ or -] standard deviation (SD) unless otherwise specified. Normal distribution of R2* value was tested using the Kolmogorov-Smirnov test. ANOVA and least significant difference t -test were used to compare R2* values among different groups and Pearson or Spearman's correlation analysis was used to correlate R2* values with the CA IX and VEGF expression. Two-sided P < 0.05 was considered statistically significant.

Results

Clinical characteristics of patients

Ninety-eight female patients (age range, 28–74 years; mean age 51.2 [+ or -] 13.5 years; median, 52 years) with 98 lesions were included in this study. Axillary lymph node metastases were detected in 48 patients. The mean diameter of the lesions was 16.5 [+ or -] 7.2 mm, with a median of 18 mm (range, 8–33 mm). Among 98 lesions, 56 lesions were ≤20 mm in size and 42 lesions were 20–50 mm. Histopathological analysis revealed that 4 lesions were in Grade I, 62 lesions were in Grade II, and 32 lesions in Grade III.

R2* value of blood oxygenation level-dependent magnetic resonance imaging

On BOLD-MRI, IDCs were heterogeneous intensity [Figure 1] and [Figure 2]. The mean R2* value of 98 lesions was 52.8 [+ or -] 18.6 Hz. Kolmogorov-Smirnov test ( Z = 0.093, P = 0.094) suggests that the samples follow a normal distribution. There was no significant correlation between the R2* values and age ( r = 0.073, P = 0.478). As shown in [Table 1], there was no significant correlation between the R2* values, BMI, or histological grade. The R2* values of tumor with the size ≤20 mm were significantly less than the R2* values of tumor with the size >20 mm. And the R2* values in patients with axillary lymph node metastasis were significantly more than the R2* values in patients without axillary lymph node metastasis.{Figure 1}{Figure 2}{Table 1}

Blood oxygenation level-dependent magnetic resonance imaging and carbonic anhydrase IX expression

As demonstrated in [Figure 1] and [Figure 2], CA IX was predominantly stained in the cytoplasm but slightly in the plasma membranes.[sup][13],[14] Immunostaining demonstrated negative CA IX expression in 12 lesions, weakly positive in 17 lesions, and moderately and strongly positive in 28 and 41 lesions. [Table 2] demonstrates that there were significant differences in the R2* values with deferent CA IX levels ( F = 13.915, P < 0.001). R2* values significantly increased with CA IX levels, but R2* values in negative-CA IX group is similar to R2* values in weakly positive group. Spearman correlation analysis showed the R2* values positively correlated with CA IX ( r = 0.696, P < 0.001).{Table 2}

Blood oxygenation level-dependent magnetic resonance imaging and vascular endothelial growth factor expression

As shown in [Figure 1] and [Figure 2], VEGF staining was predominantly in the cytoplasm. Immunostaining demonstrated 8 lesions in negative VEGF expression, 18 lesions in weakly positive expression, 34 and 38 lesions in moderately and strongly positive expression. Spearman correlation analysis suggested a weak positive correlation between VEGF and CA IX expression ( r = 0.291, P = 0.004). ANOVA analysis [Table 3] revealed that there were not significant differences in the R2* values among four VEGF levels ( F = 1.895, P = 0.136), but the R2* values in the moderately positive group were significantly higher than R2* values in the weakly positive group ( t = 2.407, P = 0.020). Spearman correlation analysis showed that the R2* value did not significantly correlate with VEGF levels ( r = 0.110, P = 0.281).{Table 3}

Discussion

In this study, we studied the correlation of BOLD-MRI with CA IX and VEGF in breast IDC and we found R2* values of BOLD-MRI positively correlated with CA IX but not with VEGF.

As the intrinsic hypoxia markers, CA IX is quite important in cancer progression and its abundance in tumors has prognostic and predictive value.[sup][3],[4],[11] Molecular imaging with a fluorescent antibody targeting CA IX can successfully detect hypoxic ductal carcinoma in situ of the breast.[sup][15] The primary source of contrast in BOLD-MRI is endogenous, paramagnetic deoxyhemoglobin which increases the MR transverse relaxation rate (R2* value) of water in the blood and surrounding tissues, thus BOLD-MRI contrast is sensitive to pO[sub]2 in tissues adjacent to perfused vessels.[sup][16] Rakow-Penner et al .[sup][17] suggest that BOLD contrast can consistently be detected in the healthy breast using a robust protocol including a single-shot fast spin-echo (SSFSE) sequence and a gradient-echo (GRE) pulse sequence. We found IDC on BOLD-MRI had a relative heterogeneous R2* intensity. We speculated that the heterogeneous R2* intensity was caused by the heterogeneous distribution of oxygen pressure and neovessels in IDC.[sup][2] Our results showed the mean R2*values in IDC were similar with the baseline R2* value in chemically induced rat mammary tumors.[sup][18] Liu et al .[sup][19] demonstrated that R2* value correlated with hypoxia inducible factor-1a. And our results showed the R2* values in IDC increased with the CA IX level and positively correlated with the CA IX levels. These suggest that BOLD-MRI can be used to predicting the hypoxic status of IDC. Moreover, we noticed there was no significantly difference of R2* values in CA IX-negative group and CA IX-weakly positive group. We speculated that this may be because of small included numbers in each group or pO[sub]2 between these two groups was similar. IDC often was heterogeneous intensity on BOLD-MRI; however, relatively higher intensity in normal breast parenchyma and the much lower intensity in the fatty tissue of breast were often observed. This can be explained by the normal breast parenchyma maybe having better tissue oxygenation than the tumor. However, it is unknown whether the low signal of breast fatty tissue is caused by the low blood supply and low pO[sub]2.

Recently, there have been increased interests in using MRI to assess tumor angiogenesis. Zhang et al .[sup][20] suggest that DCE-MRI parameters help predict rectal carcinoma angiogenesis measured by VEGF expression. However, Su et al .[sup][8] did not found any correlation of DCE-MRI parameters with microvessel density and VEGF for assessment of angiogenesis in breast cancer. Our results demonstrated a positive correlation between VEGF and CA IX expression in breast IDC and the R2* value in the moderately positive group is significantly higher than R2* value in the weakly positive group, but no significant correlation was found in R2* value and VEGF level. This may be because the multi-echo GRE sequence of BOLD-MRI decouples the effect of flow perfusion from deoxyhemoglobin.[sup][2] Since R2* values correlate with CA IX, but not with EGFR, we think that BOLD-MRI is more sensitive to diffusion-related (chronic) hypoxia than to perfusion-related (acute) hypoxia.

Breast IDC is a heterogeneous tumor that has variable behavior, outcome, and treatment response. Prognostic factors are quite important information for the evaluation and treatment to IDC. Yanai et al .[sup][21],[22] suggested that higher BMI might influence aggressive tumor characteristics in women with breast cancer. However, no correlation between BMI and R2* value was found in our patients. Tumor size is a valuable prognostic factor of breast cancer. Razek et al .[sup][23] showed ADC of IDC negatively correlated with tumor size. Our results showed that compared with IDC in size ≤20 mm, R2* values in IDC in size >20 mm significantly increased. We thought this was because the tumor with the larger size may be the more hypoxia. The histological grade is useful in clinical practice to assess the behavior of neoplasia. McPhail and Robinson [sup][18] showed that there was no significant correlation between tumor grade and tumor R2* value in rat mammary tumors. In our research, R2* value in Grade II was similar to Grade III. The presence of metastasis in axillary lymph node is the most important single predictor of long-term survival in patients with breast cancer. Razek et al. [sup][23] showed lower ADC values correlated with positive lymph node metastasis. We found that R2* value in patients with axillary lymph node metastasis is significantly higher than R2* without axillary lymph node metastasis. This predictive model may decrease the need for surgical staging of axilla in patients with breast cancer.

There are several limitations in this research. Only IDC is included in this research; the relation between R2* value and hypoxia, angiogenesis in breast cancer with other histological types such as lobular carcinoma, requires a further study. We did not measure pO[sub]2 with the Eppendorf polarographic electrode, so the correlation of R2* values and pO[sub]2 is not clear. In the case of hypoxia, it is important to remember that if the tumor stays hypoxic throughout the course of a treatment, in the follow-up study, we will observe the prognostic potential of R2* with respect to outcome of neoadjuvant chemotherapy in patients with breast cancer.

In conclusion, for IDC, R2* values of BOLD-MRI were related to CA IX levels, but not VEGF. BOLD-MRI could detect chronic hypoxia in breast IDC.

Financial support and sponsorship

This research was supported by grants from the Chinese National Scientific Research Foundation (No. 30900364), Beijing Medicine and Technology Researching Foundation (No. Z101107050210032) and Capital Medical University Fundamental-Clinical Research Foundation (No. 15JL03).

Conflicts of interest

There are no conflicts of interest.

References

1. Penn JS. Retinal and Choroidal Angiogenesis. Netherlands: Springer; 2008. p. 119. [Last retrieved on 2010 Jun 26]. doi:10.1007/978-1-4020-6780-8.

2. Padhani AR, Krohn KA, Lewis JS, Alber M. Imaging oxygenation of human tumours. Eur Radiol 2007;17:861-72. doi: 10.1007/s00330-006-0431-y.

3. Wykoff CC, Beasley N, Watson PH, Campo L, Chia SK, English R, et al. Expression of the hypoxia-inducible and tumor-associated carbonic anhydrases in ductal carcinoma in situ of the breast. Am J Pathol 2001;158:1011-9. doi: 10.1016/S0002-9440(10)64048-5.

4. Hussain SA, Ganesan R, Reynolds G, Gross L, Stevens A, Pastorek J, et al. Hypoxia-regulated carbonic anhydrase IX expression is associated with poor survival in patients with invasive breast cancer. Br J Cancer 2007;96:104-9. doi: 10.1038/sj.bjc.6603530.

5. Hoeben A, Landuyt B, Highley MS, Wildiers H, Van Oosterom AT, De Bruijn EA. Vascular endothelial growth factor and angiogenesis. Pharmacol Rev 2004;56:549-80. doi: 10.1124/pr.56.4.3.

6. Wang Y, Zhang X, Cao K, Li Y, Li X, Qi L, et al. Diffusion-tensor imaging as an adjunct to dynamic contrast-enhanced MRI for improved accuracy of differential diagnosis between breast ductal carcinoma in situ and invasive breast carcinoma. Chin J Cancer Res 2015;27:209-17. doi: 10.3978/j.issn.1000-9604.2015.03.04.

7. Gulliksrud K, Mathiesen B, Galappathi K, Rofstad EK. Quantitative assessment of hypoxia in melanoma xenografts by dynamic contrast-enhanced magnetic resonance imaging: Intradermal versus intramuscular tumors. Radiother Oncol 2010;97:233-8. doi: 10.1016/j.radonc.2010.09.005.

8. Su MY, Cheung YC, Fruehauf JP, Yu H, Nalcioglu O, Mechetner E, et al. Correlation of dynamic contrast enhancement MRI parameters with microvessel density and VEGF for assessment of angiogenesis in breast cancer. J Magn Reson Imaging 2003;18:467-77. doi: 10.1002/jmri.10380.

9. Ogawa S, Lee TM. Magnetic resonance imaging of blood vessels at high fields : In vivo an d in vitro measurements and image simulation. Magn Reson Med 1990;16:9-18. doi: 10.1002/mrm.1910160103.

10. Prielmeier F, Nagatomo Y, Frahm J. Cerebral blood oxygenation in rat brain during hypoxic hypoxia. Quantitative MRI of effective transverse relaxation rates. Magn Reson Med 1994;31:678-81. doi: 10.1002/mrm.1910310615.

11. Neugarten J. Renal BOLD-MRI and assessment for renal hypoxia. Kidney Int 2012;81:613-4. doi: 10.1038/ki.2011.462.

12. Loncaster JA, Harris AL, Davidson SE, Logue JP, Hunter RD, Wycoff CC, et al. Carbonic anhydrase (CA IX) expression, a potential new intrinsic marker of hypoxia: Correlations with tumor oxygen measurements and prognosis in locally advanced carcinoma of the cervix. Cancer Res 2001;61:6394-9. doi: 10.1158/0008-5472.

13. Kim SJ, Rabbani ZN, Vollmer RT, Schreiber EG, Oosterwijk E, Dewhirst MW, et al. Carbonic anhydrase IX in early-stage non-small cell lung cancer. Clin Cancer Res 2004;10:7925-33. doi: 10.1158/1078-0432.CCR-04-0636.

14. Sedlakova O, Svastova E, Takacova M, Kopacek J, Pastorek J, Pastorekova S. Carbonic anhydrase IX, a hypoxia-induced catalytic component of the pH regulating machinery in tumors. Front Physiol 2014;4:400. doi: 10.3389/fphys.2013.00400.

15. van Brussel AS, Adams A, Vermeulen JF, Oliveira S, van der Wall E, Mali WP, et al. Molecular imaging with a fluorescent antibody targeting carbonic anhydrase IX can successfully detect hypoxic ductal carcinoma in situ of the breast. Breast Cancer Res Treat 2013;140:263-72. doi: 10.1007/s10549-013-2635-6.

16. Chopra S, Foltz WD, Milosevic MF, Toi A, Bristow RG, Menard C, et al. Comparing oxygen-sensitive MRI (BOLD R2*) with oxygen electrode measurements: A pilot study in men with prostate cancer. Int J Radiat Biol 2009;85:805-13. doi: 10.1080/09553000903043059.

17. Rakow-Penner R, Daniel B, Glover GH. Detecting blood oxygen level-dependent (BOLD) contrast in the breast. J Magn Reson Imaging 2010;32:120-9. doi: 10.1002/jmri.22227.

18. McPhail LD, Robinson SP. Intrinsic susceptibility MR imaging of chemically induced rat mammary tumors: Relationship to histologic assessment of hypoxia and fibrosis. Radiology 2010;254:110-8. doi: 10.1148/radiol.2541090395.

19. Liu M, Guo X, Wang S, Jin M, Wang Y, Li J, et al. BOLD-MRI of breast invasive ductal carcinoma: Correlation of R2* value and the expression of HIF-1a. Eur Radiol 2013;23:3221-7. doi: 10.1007/s00330-013-2937-4.

20. Zhang XM, Yu D, Zhang HL, Dai Y, Bi D, Liu Z, et al. 3D dynamic contrast-enhanced MRI of rectal carcinoma at 3T: Correlation with microvascular density and vascular endothelial growth factor markers of tumor angiogenesis. J Magn Reson Imaging 2008;27:1309-16. doi: 10.1002/jmri.21378.

21. Yanai A, Miyagawa Y, Murase K, Imamura M, Yagi T, Ichii S, et al. Influence of body mass index on clinicopathological factors including estrogen receptor, progesterone receptor, and Ki67 expression levels in breast cancers. Int J Clin Oncol 2014;19:467-72. doi: 10.1007/s10147-013-0585-y.

22. Turkoz FP, Solak M, Petekkaya I, Keskin O, Kertmen N, Sarici F, et al . The prognostic impact of obesity on molecular subtypes of breast cancer in premenopausal women. J BUON 2013;18:335-41.

23. Razek AA, Gaballa G, Denewer A, Nada N. Invasive ductal carcinoma: Correlation of apparent diffusion coefficient value with pathological prognostic factors. NMR Biomed 2010;23:619-23. doi: 10.1002/nbm.1503.
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Title Annotation:Original Article
Author:Wang, Ying; Liu, Min; Jin, Mu-Lan
Publication:Chinese Medical Journal
Article Type:Report
Geographic Code:9CHIN
Date:Jan 1, 2017
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