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This study aims to determine feasibility and utility of copper-64(II) chloride (64CuCl2) as a tracer for positron emission tomography (PET) of copper metabolism imbalance in human Wilson’s disease (WD).
Atp7b−/− mice, a mouse model of human WD, were injected with 64CuCl2 intravenously and subjected to PET scanning using a hybrid PET-CT (computerized tomography) scanner, with the wild-type C57BL mice as a normal control. Quantitative PET analysis was performed to determine biodistribution of 64Cu radioactivity and radiation dosimetry estimates of 64Cu were calculated for PET of copper metabolism in humans.
Dynamic PET analysis revealed increased accumulation and markedly reduced clearance of 64Cu from the liver of the Atp7b−/− mice, compared to hepatic uptake and clearance of 64Cu in the wild-type C57BL mice. Kinetics of copper clearance and retention was also altered for kidneys, heart, and lungs in the Atp7b−/− mice. Based on biodistribution of 64Cu in wild-type C57BL mice, radiation dosimetry estimates of 64Cu in normal human subjects were obtained, showing an effective dose (ED) of 32.2 μ (micro)Sv/MBq (weighted dose over 22 organs) and the small intestine as the critical organ for radiation dose (61 μGy/MBq for males and 69 μGy/MBq for females). Radiation dosimetry estimates for the patients with WD, based on biodistribution of 64Cu in the Atp7b−/− mice, showed a similar ED of 32.8 μ (micro)Sv/MBq (p= 0.53), with the liver as the critical organ for radiation dose (120 μSv/MBq for male and 161 μSv/MBq for female).
Quantitative PET analysis demonstrates abnormal copper metabolism in the mouse model of WD with improved time–resolution. Human radiation dosimetry estimates obtained in this preclinical study encourage direct radiation dosimetry of 64CuCl2 in human subjects. The results suggest feasibility of utilizing 64CuCl2 as a tracer for noninvasive assessment of copper metabolism in WD with PET.
Copper metabolism is an important physiological process in humans. Copper is an essential element, which is required for normal function of numerous key metabolic enzymes, however in excess copper is toxic [1, 2]. Absorption, distribution, and clearance of copper are tightly regulated [3, 4] by a finely-tuned network of copper transporters [5, 6]. In humans, malfunction of copper transporters causes disruption of copper homeostasis and severe disorders  which include WD caused by a mutation of the ATP7B (ATPase, Cu+transporting, beta polypeptide) gene [8, 9] and Menkes disease caused by a mutation of the ATP7A (ATPase, Cu+transporting, α polypeptide) gene [10–12]. WD is an autosomal-recessive disorder with a birth incidence rate of approximately 1:30,000 and about 1% of population being carriers of ATP7B gene mutation . Accumulating evidence suggests that the imbalance of copper metabolism also significantly contributes to the pathogenesis of such human diseases as Alzheimer’s disease , cancer , and cardiovascular disease .
Mechanistic understanding of the role of copper in pathophysiology of human diseases requires a non-invasive assessment of copper metabolism in vivo. Previously, radioactive copper was used to study copper absorption and distribution in rodents by counting radioactivity of body fluids or tissues ex vivo [17–19]. These studies have yielded useful information about copper distribution between tissues, but real-time copper fluxes in vivo remain largely uncharacterized. Kinetics of copper uptake and clearance may vary greatly between different organs and may inform on disease onset and progression. Thus, in recent years, there has been a considerable interest in developing quantitative approaches to measure copper in vivo [20–23].
Chemical indicators and probes in conjunction with microscopic examination have been employed for studying copper status in cells, but they are not yet suitable for direct analysis of copper flow in living animals or humans. Chemical agents for magnetic resonance imaging (MRI) [20, 21] are useful for static quantification of copper ions in animal organs or tissues, but may have low sensitivity for tracking flow of a trace amount of copper in vivo. The application of promising fluorescent tracers [22, 23] for the analysis of copper flow in live organisms needs to overcome limited tissue penetration, high background fluorescence, and quenching of fluorescence signals. To enable accurate understanding of copper physiology and clinical applications, it is necessary to search for additional imaging agents allowing quantitative and longitudinal analysis of copper flow in vivo, particularly noninvasive assessment of copper metabolism in humans.
Positron emission tomography (PET) is a highly sensitive and quantitative molecular imaging technology, which is particularly well suited for systemic analysis of copper metabolism in animals and humans. Several positron-emitting copper isotopes are currently available  which include 62Cu (t1/2 9.74 m, 98% β+) and 64Cu (t1/2 12.7 h, 17% β+). The goal of this study was to determine feasibility of using 64CuCl2 as a tracer for noninvasive assessment of copper metabolism imbalance in WD with PET. To reach this goal, we utilized Atp7b−/− mice, an established animal model for WD. Specifically, we aimed: (1) to determine biodistribution of 64Cu in Atp7b−/− mice injected with 64CuCl2 intravenously, in comparison with the control C57BL mice; and (2) based on biodistribution in mice, obtain 64Cu radiation dosimetry estimates for PET of copper metabolism in humans. By performing dynamic PET, we obtained the first real-time measurements of 64Cu distribution in the organs or tissues of Atp7b−/− mice. The human radiation dosimetry estimates of 64Cu were also calculated, which encourage direct radiation dosimetry and PET of copper metabolism in the patients with WD using 64CuCl2 as a tracer.
The Atp7b−/− mice (5–6 weeks old, N=4, two male and two female) and the control wild-type C57BL mice (12–13 weeks old, N=4, two male and two female) were transferred from Johns Hopkins University (Baltimore, MD, USA) to UT Southwestern Medical Center (Dallas, TX, USA) and used for this study at the age of 7–8 weeks (Atp7b−/−) or 15–16 weeks old (C57BL mice). Copper-64 produced via 64Ni(p,n)64Cu on a biomedical cyclotron was purchased from Washington University (St Louis, MO, USA) in the form of 64CuCl2 in 0.1 N HCl solution. The specific activity of 64Cu was around 6.9±2.5 Ci/μmol.
All animal experiments were conducted under the protocol approved by the UT Southwestern Institutional Animal Care and Use Committee. PET of mice was performed with a Siemens Inveon PET/computerized tomography (CT) Multimodality System, using a protocol modified from those described previously [25, 26]. Calibration of the PET/CT scanner was performed with an in-house manufactured phantom containing a dose of 64CuCl2 as a radiation source. Briefly, mice were anesthetized using 3% isoflurane at room temperature and placed in spread–supine position on the imaging bed under 2% isoflurane anesthesia for the duration of the imaging. Initially, a helical CT scan was acquired (80 kV, 500 μA) with a pixel size of ~0.1 mm in order to create an anatomical image that was subsequently used for attenuation correction of the PET emission data. Following conclusion of the CT scan, mice were injected with the tracer 64CuCl2 (74 kBq or 2 μCi/g body weight), diluted with normal saline containing 0.9% sodium chloride into a total volume of 100 μL intravenously via the tail vein. Immediately after administration of the tracer, dynamic whole body data acquisition was started for 1 h with the liver in the center of the field of view. In addition, static whole body imaging was performed at 2 and 24 h post injection of the tracer, which consisted of two overlapping frames of 15 min duration for each frame. PET images were reconstructed using the ordered subsets expectation maximization 3D algorithm and analyzed using the Inveon Research Workplace software (Siemens) which allows fusion of CT and PET image volumes, the re-slicing of fused images into arbitrary views and the definition of regions of interests (ROIs) in order to obtain time-activity curves that were further processed as described below.
ROIs for various organs were defined on serial axial images and non-decay corrected time–activity curves were obtained for the following organs: brain, heart, lung, liver, kidneys, bladder, small intestine, upper large intestine, lower large intestine, testis, muscle, and blood (blood pool of large blood vessels in the superior mediastinum). Time–activity curves were extended to 24 h by combining the initial dynamic scan with scans obtained at 2 and 24 h post injection. The residence time for each organ was then calculated as the integral under the time–activity curve normalized to the injected activity and multiplying the result with the weight of the organ. The absorbed dose to the organs was calculated assuming homogeneous distribution of the activity throughout the organ. The residence time of the remainder activity was accounted for by subtracting the residence time determined for the organs from the inverse of the decay constant for 64Cu (18.3 h−1). Since blood is not a source organ of medical internal radionuclide dose, blood activity was assigned to the remainder of the body. Subsequently, these residence times were used together with the OLINDA software [27, 28] in order to estimate the dose to multiple organs. The OLINDA software considers all doses from a source to a specific target organ contributed by the various decay schemes of 64Cu (β+, β−, EC, and r) and yields the effective dose (ED), which is representative of the overall radiation dose to a subject from PET imaging.
In order to assess significant differences in 64Cu biodistribution between Atp7b−/− and C57BL wild-type mice, a 2×(8) mixed-design analysis was conducted, where the between-subjects factor represents the group (Atp7b−/−, C57BL mice) and the within-subjects factor represents the radiation dose in regions that showed either the highest 64Cu radioactivity or regions known to be most sensitive to radiation (liver, kidney, small intestines, upper large bowel, lower large bowel, lungs, heart, gonads). The overall test was subsequently followed up by post-hoc unpaired t tests between the two groups for individual regions. Finally, we applied an unpaired t test in order to determine whether there are significant differences in the calculated ED values between males and females with WD and control subjects. A p value <0.05 was considered to represent statistical significance.
Copper metabolism in the liver is regulated by a single copper-transporting ATPase Atp7b, whereas in most of the other tissues two Cu-ATPases, Atp7a and Atp7b work together to maintain copper balance. In normal liver, the function of Atp7b is to transport copper into the secretory pathway for incorporation into ceruloplasmin and to export excess copper into the bile. Consequently, in Atp7b−/− mice, we expected to observe poor copper excretion from the liver due to Atp7b inactivation leading to higher levels of hepatic copper. Based on earlier work with WD patients [29, 30], the uptake of copper into the Atp7b−/− liver was also expected to be elevated, although the mechanism behind this increase remains unknown. Since the time-resolved quantitative analysis of copper uptake has never been done in live Atp7b−/− mice, we performed measurements of 64Cu accumulation using dynamic PET imaging in order to assess the kinetics of copper uptake in a pre-clinically relevant time frame.
Whole body images from dynamic imaging at 0–1 h post-injection showed intense 64Cu radioactivity in the liver and much lower intensity in other organs or tissues, for both the control C57BL and the Atp7b−/− mice (Fig. 1). There was a continued accumulation of 64Cu in the liver of Atp7b−/− mice, whereas initial rapid uptake of 64Cu in the liver of the control C57BL mice was followed by a gradual clearance of the tracer from the liver to the intestines via hepatobilliary clearance pathway. Static whole body images at 24 h post-injection showed much higher 64Cu radioactivity in the liver of the Atp7b−/− mice than control C57BL mice (Fig. 1). Time-activity curves demonstrated that the initial rate of hepatic copper uptake was significantly higher in Atp7b−/− mice compared to control (Fig. 2). The continuing copper accumulation resulted in a marked difference of hepatic 64Cu radioactivity between the Atp7b−/− and control C57BL mice at 24 h post-injection. The percentage of injected dose per gram %ID/g of hepatic 64Cu uptake was significantly higher in Atp7b−/− mice as compared to C57BL mice (52.3±6.6 vs. 10.9±1.7, p<0.001; Fig. 3).
Among extrahepatic organs, kidneys have a relatively high level of Atp7b but also express Atp7a. Consequently, we studied whether the loss of Atp7b was associated with a rapid copper accumulation and reduced clearance similar to that observed in the liver. Our measurements revealed that this was not the case. Renal uptake of 64Cu in the Atp7b−/− in the initial 60 min was similar to those of the control C57BL mice (Fig. 2), with the 64Cu radioactivity gradually decreasing in both animal strains. At 24 post-injection of the tracer, the renal %ID/g of 64Cu was significantly lower in the Atp7b−/− mice as compared to controls (1.93±0.67 vs. 4.08± 0.86, p=0.01, Fig. 3). There was no simultaneous increase of 64Cu radioactivity in the urinary bladder, and the amount of 64Cu radioactivity in the urinary bladder was low, indicative of the lack of significant copper excretion via this route.
64Cu radioactivity in several other organs of Atp7b−/− mice was lower than that determined in control C57BL mice (Fig. 3) at 24 h post-injection, which was independent of some initial differences in the distribution kinetics. For example, in the first hour post-injection of the tracer, Cu64 radioactivity in both the heart and lungs of Atp7b−/− mice was higher than those in C57BL mice. However, at 24 h post-injection, the %ID/g of 64Cu in the heart of Atp7b−/− mice was significantly lower than those in the C57BL mice (1.11±0.50 vs. 2.42±0.67, p=0.02), but similar for the lungs (2.06±0.62 vs. 2.64±0.34, p=0.15; Fig. 3). Finally, quantitative analysis revealed consistently lower 64Cu radioactivity at all times in the brain of Atp7b−/− mice as compared to C57BL mice, which was significant at 24 h post-injection (0.28+0.05 vs. 0.63+0.17, p<0.01).
The residence times (see Table 1) were calculated from kinetic 64Cu PET data in C57BL wild-type and Atp7b−/− mice. Based on these residence times, organ-absorbed radiation dose estimates in humans were calculated as shown in Table 2. The results indicate that, whereas in control subjects the critical organ is the small intestine (61 μGy/MBq for males and 69 μGy/MBq for females), in patients with WD the critical organ is the liver (120 and 161 μGy/MBq for males and females, respectively, Fig. 4). Application of a mixed-design ANOVA showed a significantly higher absorbed dose only for the liver (p=0.003) in patients with WD. Administration of 5 MBq/kg (0.14 mCi/kg) of 64CuCl2 for PET studies results in a total PET dose of 9.4±0.96 mSv in the control group and a similar dose of 10.1+10.04 mSv in patients with WD (p=0.53, Table 3). Figure 5 shows the total PET dose for both genders and the two groups under study. Finally, the effective dose originating from PET imaging using 64CuCl2 was only 20% higher than that determined in 2-deoxy-2-[18F]fluoro-D-glucose ([18F]FDG studies; 32 vs. 27 μSv/MBq) . Moreover, the average dose to the critical organ (small intestines for control subjects or liver for patients with WD) is about half (63 μSv/MBq and 140 μSv/MBq, respectively) of that compared with the critical organ for [18F]FDG, which is the urinary bladder (220 μSv/MBq). Thus, the overall radiation dose for a PET study using 64CuCl2 is comparable to that for the established [18F]FDG PET.
Systemic analysis of whole body copper metabolism is important for understanding of molecular mechanisms that maintain copper homeostasis in humans. In particular, identifying temporal and spatial differences in copper distribution is needed in order to elucidate the pathophysiology of copper misbalance in diseases such as WD [6, 7]. In recent years, significant progress has been made in characterization of cellular machinery that controls copper homeostasis; however, little is known about real-time copper distribution between tissues in either normal person or in the patients with copper-related disorders.
Previously, attempts were made to assess copper metabolism in the patients diagnosed with WD using a nuclear scanner and 64Cu or 67Cu isotopes [29, 30, 32, 33] and in Long–Evans cinnamon rats, a rat model of WD with a microPET scanner . In the 1960s, Osborn et al.  conducted abdominal scintiscans in 27 patients with WD (six in the presymptomatic, six in the hepatic, and 15 in the neurological stages of the disease) using a Picker Magnascanner. The patients were injected with 0.2–0.6 mCi of 64CuCl2 in normal saline as a single intravenous injection following withdrawal of blood into the syringe to ensure adequate mixing with plasma proteins before injection. It was found that the hepatic concentrating power for copper decreased along with progression of the disease and the extrahepatic (presumably renal) deposits of radioactivity become more conspicuous and the general tissue level of radioactivity increase. However, limited spatial resolution of the scintiscanner available at that time did not allow more detailed and quantitative analysis of copper radioactivity at various tissues and organs. Radiation dosimetry of 64CuCl2 or 67CuCl2 was not reported in the literature, most likely because the limited spatial resolution of the instruments used in the previous studies prevented measurements of the radioactive copper concentration in specific organs or tissues. Improved spatial resolution of a modern animal PET/CT scanner made it possible to conduct preclinical radiation dosimetry based on biodistribution of 64Cu radioactivity in animals prior to direct radiation dosimetry in human subjects.
Recent advances in hybrid PET-CT, as well as hybrid PET-MRI are expected to invigorate interest in utilization of PET for study of copper metabolism in vivo. PET/CT is particularly suitable for non-invasive assessment of whole body copper metabolism, but the lack of a tracer approved for use in humans has hampered application of PET for mechanistic investigations of molecular mechanisms of copper misbalance in human diseases. In the clinic, the high sensitivity of PET combined with superior spatial resolution of CT and MRI [35, 36] make it ideal for noninvasive, time-dependant analysis of copper metabolism in humans.
To develop a tracer for PET of copper metabolism in humans, we assessed copper distribution in Atp7b−/− mice, an established mouse model of WD , using a state of the art animal PET-CT scanner (Siemens Inveon PET/CT Multimodality System). High spatial resolution of the PET-CT scanner allowed for the first time kinetic analysis of copper distribution in various organs or tissues in living animals, thus improving upon the earlier studies where only radioactive copper flow to the liver could have been reliably assessed. As expected, rapid uptake and accumulation of copper was found in the liver of Atp7b−/− mice in association with dramatically reduced hepatobilliary clearance compared with that in wild-type C57BL mice, as visualized on the PET-CT images (Fig. 1) and time–activity curves (Fig. 2). Consistent with the early reports in presymptomatic WD patients, the 6-week-old Atp7b−/− mice show increased kinetics of hepatic copper uptake, thus further validating this mouse model of WD. Although the Atp7b−/− mice used in this study were younger than the control wild-type C57BL mice (5–6 weeks old versus 12–13 weeks old), we do not expect significant difference of copper metabolism in the wild-type C57BL mice aged 5–6 or 12–13 weeks old based on our observation from other experiments.
In contrast to the liver, 64Cu radioactivity from extra-hepatic tissues, including brain, kidneys, lungs, and heart, is significantly lower in the Atp7b−/− mice compared to control C57BL mice (Figs. 2 and and3).3). The reduced 64Cu radioactivity in the Atp7b−/− extrahepatic tissues may be caused by hepatic sequestration. Since copper taken by the liver is normally transported by Atp7b−/− to ceruloplasmin and other copper-containing proteins in the secretory pathway; the diminished copper uptake by extrahepatic tissues implies the role for such cupro-proteins in bioavailability of copper to these tissues. The role for cupro-proteins in copper delivery to extrahepatic tissues was earlier suggested in the experiments with rats , but remained controversial due to the lack of marked changes in copper metabolism in cerulo-plasmin-deficient mice .
The PET-CT studies have also demonstrated differences between tissues in the rate of copper clearance. This could be due to the presence (and potential change in the expression/activity) of the second copper–efflux system, Atp7a. For example, the efflux of copper from kidneys is expected to be decreased by Atp7b gene knock-out; however, our data revealed faster initial rate of copper efflux from Atp7b−/− kidneys compared to control. This could be due to a significant change in the intracellular localization of Atp7a. Normally, in renal tubules ATP7A is located intra-cellularly, however in Atp7b−/− mice it is redistributed towards the basolateral membrane consistent with the role in copper efflux . And yet, with age copper begins to accumulate in kidneys and in old Atp7b−/− mice (>9 months) renal copper is higher than in control , illustrating insufficiency of compensatory mechanisms. Overall, tissue-specific responses to copper deficiency and copper overload are well known [42–44], but the molecular mechanism behind tissue-specific responses to changing copper remains largely unexplored. The ability to measure the kinetics of copper distribution between tissues in real-time may greatly aid to understanding of such responses and have important implication for better tuning of copper supplement or chelating therapies.
Multiple positron emitting copper isotopes are available for tracking copper flow in vivo with PET, which include 60Cu (t1/2 23.7 min, 93% β+, 7% EC), 61Cu (t1/2 3.32 h, 60% β+, 40% EC), 62Cu (t1/2 9.74 m; 98% β+, 2% EC), and 64Cu (t1/2 12.7 h, 17.4% β+, 43% EC, 39% β−). 64Cu in the form of 64CuCl2 can be potentially used as a simple tracer to assess copper metabolism in humans because (1) its relatively long half-life (t1/2 12.7 h) is desirable for tracking copper flow in vivo with PET; (2) it can be conveniently produced on a biomedical cyclotron and is commercially available in a ready-to-be-used chemical form (64CuCl2); and (3) 64CuCl2 was used for assessing copper metabolism in the normal human subjects and the patients diagnosed with WD [29, 30, 32, 33]. Because of the 39% β− emission from 64Cu, it is essential to determine radiation dosimetry of 64CuCl2 to ensure the safety of its use in humans. Based on a method used in the previous study in humans , we diluted 64CuCl2 in 0.1 N HCl with saline containing 0.9% sodium chloride for intravenous administration of this tracer to the mice. Following intravenous administration, it is expected that 64CuCl2 will immediately interact with abundant copper-binding proteins or molecules present in the plasma and cellular components of the blood. Absorption and distribution of 64Cu in a specific organ or tissue will be governed by a sophisticated regulation mechanism related to perfusion of the organ or tissue and functional activity of the copper transporters and chaperons in the cells or tissues. Although copper handling machinery is highly conserved between human and rodents, the copper-carrying proteins are not identical and the difference in regulation and metabolic needs of copper by various organs exists in different species. The data from this study might be subject to errors, considering difference of copper metabolism among different species of animals. Given the fact that 64Cu(II) in the form of 64CuCl2 is easily accessible by other copper-transporting molecules in vivo after its injection, we regard 64CuCl2 as an ideal source of 64Cu(II) for tracking copper metabolism in vivo. On the other hand, we recognize that additional studies are needed to compare 64CuCl2 with 64Cu compounds in other chemical forms such as 64Cu-citrate and 64Cu-labeled human albumin to determine their roles in PET studies of copper metabolism in humans. Nevertheless, the data from this study has provided useful insights for further investigations of copper metabolism in humans using the noninvasive imaging technique of PET.
Based on its biodistribution in C57BL wild-type mice, human radiation dosimetry estimates of 64CuCl2 were calculated to determine a safe dose for direct radiation dosimetry in humans. Radiation dose to gallbladder was not calculated because of poor anatomic localization of gall-bladder on the CT images of the mice. The results of this preclinical study predict a radiation dose of 64CuCl2 comparable to that of [18F]FDG, when 5 MBq/kg (0.14 mCi/kg) of 64CuCl2 is administered for PET in normal human subjects. Human dosimetry estimates obtained in our study may allow injection of 5 MBq/kg or 0.14 mCi/kg of 64CuCl2 (350 MBq or 9.8 mCi of 64CuCl2 for a 70-kg adult) for clinical PET scan in a normal human subject. However, in order to comply with the Code of Federal Regulation which limits the dose to the critical organ for a single study to 5 rem, a reduced tracer dose of 4 MBq/kg or 0.11 mCi/kg of 64CuCl2 (280 MBq or 7.8 mCi of 64CuCl2 for a 70-kg adult) may be used for PET imaging of copper metabolism in patients diagnosed with or suspected for WD. This needs to be adjusted following direct radiation dosimetry of 64CuCl2 in humans. Because the amount of copper ions in a tracer dose of 64CuCl2 is very small compared with the amount of copper (0.3–0.8 mg/d) absorbed from a normal diet , we do not expect significant toxicity or side effects from copper ions contained in a tracer dose of 64CuCl2 for PET in humans.
Genetic testing alone is insufficient for predicting the severity and course of WD, as patients with identical mutations may show markedly different phenotype. The described methodology may find useful application in real-time assessing of copper metabolism misbalance in the patients with WD and other copper metabolic disorders such as Menkes disease caused by mutation of the Atp7a gene [10–12]. In addition, PET using 64CuCl2 as a tracer is expected to be helpful for clinical management of the patients with WD by monitoring patient’s response to copper-lowering therapy with penicillamine or other medications. Lastly, copper distribution in patients with neurological and hepatic manifestations can be measured and compared, which may contribute to better understanding of the diversity of phenotypic manifestations in WD.
Copper is required for cell proliferation and tumor angiogenesis . Biodistribution of 64Cu radioactivity was found to be different from that of [18F]FDG, a glucose analog clinically used for imaging glucose metabolism, which was cleared from body mainly through renal clearance pathway, not through hepatobilliary clearance pathway . PET using 64CuCl2 may be used for localization and assessment of tumors located in a region where use of [18F]FDG PET is limited by physiological background activity of [18F]FDG. Because copper is required for tumor growth and angiogenesis, copper-chelating drugs such as tetrathiomolybdate (TM) were tested for anticancer therapy in a phase I clinical trial . It was reported that different types of tumors had variable responses to TM treatment although molecular mechanisms for the difference in treatment response were not clear. We have previously demonstrated that human prostate cancer xenografts with increased uptake of 64CuCl2 in mice could be visualized on the PET images . Using 64CuCl2 as a tracer, PET may be used to assess status of copper metabolism of the tumors and select the patients with tumors hypermetabolic in copper metabolism for personalized copper-lowering anticancer therapy.
The authors thank Jon Anderson and Anjali Gupta for technical support in calibration of PET-CT scanner and PET-CT scanning, and Guiyang Hao for help in tracer injection. This project was funded partially by National Institutes of Health, USA (R21EB005331-01A2 to F.P; R56DK084510 to SL) and the Department of Radiology and Harold C. Simmons Comprehensive Cancer Center, at University of Texas Southwestern Medical Center at Dallas, TX, USA. The production of Cu-64 at Washington University School of Medicine is supported by NCI grant R24 CA86307.
The authors declare that they have no conflict of interest.