J Cancer 2021; 12(1):244-252. doi:10.7150/jca.49628

Research Paper

Synthesis and evaluation of 68Ga-labeled dimeric cNGR peptide for PET imaging of CD13 expression with ovarian cancer xenograft

Yi Yang1,2, Jun Zhang3 Corresponding address, Huifeng Zou2, Yang Shen2, Shengming Deng1 Corresponding address, Yiwei Wu1 Corresponding address

1. Department of Nuclear Medicine, the First Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215006, China.
2. Department of Nuclear Medicine, the Affiliated Suzhou Science & Technology Town Hospital of Nanjing Medical University, Suzhou, Jiangsu 215153, China.
3. Department of Nuclear Medicine, Taizhou People's Hospital, Taizhou, Jiangsu 225300, China.

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Yang Y, Zhang J, Zou H, Shen Y, Deng S, Wu Y. Synthesis and evaluation of 68Ga-labeled dimeric cNGR peptide for PET imaging of CD13 expression with ovarian cancer xenograft. J Cancer 2021; 12(1):244-252. doi:10.7150/jca.49628. Available from https://www.jcancer.org/v12p0244.htm

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Introduction: Previous studies have shown that peptides containing the asparagine-glycine-arginine (NGR) sequence can specifically bind to CD13 (aminopeptidase N) receptor, a tumor neovascular biomarker that is over-expressed on the surface of angiogenic blood vessels and various tumor cells, and it plays an important role in angiogenesis and tumor progression. In the present study, we aimed to evaluate the efficacy of a gallium-68 (68Ga)-labeled dimeric cyclic NGR (cNGR) peptide as a new molecular probe that binds to CD13 in vitro and in vivo.

Materials and Methods: A dimeric cNGR peptide conjugated with 1,4,7,10-tetraazacyclododecane-N,N',N'',N'''-tetraacetic acid (DOTA) was synthesized and labeled with 68Ga. In vitro uptake and binding analyses of the 68Ga- DOTA-c(NGR)2 were performed in two ovarian tumor cell lines, ES2 and SKOV3, which had different CD13 expression patterns. An in vivo biodistribution study was performed in normal mice, and micro positron emission tomography (PET) imaging was conducted in nude mice bearing ES2 and SKOV3 tumors.

Results: 68Ga-DOTA-c(NGR)2 was prepared with high radiochemical purity (>95%), and it was stable both in saline at room temperature and in bovine serum at 37°C for 3 h. In vitro studies showed that the uptake of 68Ga-DOTA-c(NGR)2 in ES2 cells was higher compared with SKOV3 cells, and such uptake could be blocked by the cold DOTA-c(NGR)2. Biodistribution studies demonstrated that 68Ga-DOTA-c(NGR)2 was rapidly cleared from blood and mainly excreted from the kidney. MicroPET imaging of ES2 tumor xenografts showed the focal uptake of 68Ga-DOTA-c(NGR)2 in tumors from 1 to 1.5 h post-injection. The high-contrast tumor visualization occurred at 1 h, corresponding to the highest tumor/background ratio of 10.30±0.26. The CD13-specific tumor targeting of the 68Ga-DOTA-c(NGR)2 was further supported by the reduced uptake of the probe in ES2 tumors by co-injection of the unlabeled cold peptide. In SKOV3 tumor models, the tumor was not obviously visible under the same imaging conditions.

Conclusions: 68Ga-DOTA-c(NGR)2 was easily synthesized, and it showed favorable CD13-specific targeting ability by in vitro data and microPET imaging with ovarian cancer xenografts. Collectively, 68Ga-DOTA-c(NGR)2 might be a potential PET imaging probe for non-invasive evaluation of the CD13 receptor expression in tumors.

Keywords: Tumor angiogenesis, NGR peptide, CD13, microPET imaging, 68Ga labeling


Aminopeptidase N, also known as cluster of differentiation 13 (CD13), is a zinc-dependent membrane-bound exopeptidase that is usually up-regulated on the endothelium of tumor neovasculature and in various solid cancers, including melanoma, prostate, ovarian, lung and breast cancer [1-4]. CD13 is a key regulator involved in angiogenesis and tumor progression, and it is also a key binding receptor for peptides containing the asparagine-glycine-arginine (NGR) sequence [5-7]. In recent years, NGR peptide-based imaging studies have become an intriguing approach in CD13-targeting diagnosis and therapy of cancer.

Ovarian cancer (OVCA), a serious threat to women's health, is characterized by high recurrence rate and high mortality. It is the third most common gynecologic malignant tumor after endometrial carcinoma and cervical cancer in China [8]. Many studies have focused on the treatment of OVCA by targeting CD13 [4, 9, 10]. However, CD13 is differentially expressed in OVCA tissues and cell lines, such as ES2 and SKOV3 cells, due to the heterogeneity of the disease. ES2 cells are intensely positive for CD13, while SKOV3 cells express CD13 at a low level [11].

Radio-labeled NGR peptides have been investigated for CD13 imaging with tumor xenografts [12-15]. The cyclic peptides have been found to be more stable than the linear ones because the former is more resistant to enzymolysis [16]. In addition, the dimeric NGR peptide shows a higher CD13 affinity than the monomer as the dimer can bind to more sites in target cells [17, 18]. In the present study, we designed and synthesized a novel 68Ga-labeled dimeric cyclic NGR (cNGR) peptide and investigated its potential for non-invasive positron emission tomography (PET) imaging of CD13 expression with OVCA mouse xenografts.

Materials and Methods

General materials

All chemicals (reagent grade), unless specifically stated, were purchased from commercial suppliers and used without further purification. DOTA-c(NGR)2 (Fig. 1) was synthesized using standard F-moc solid-phase chemistry by Sangon-Peptide Biotech Co., Ltd. (Ningbo, China) with a purity of 98.X% as analyzed by high-performance liquid chromatography (HPLC) and mass spectrometry (MS). 68GaCl3 was produced from 68Ge-68Ga radionuclide generator (ITG GmbH, Oberding, Germany) by elution with 5 mL of 0.05 M HCl.

Labeling and characterization of 68Ga-DOTA-c(NGR)2

A DOTA-c(NGR)2 stock solution of 5 mg/mL was prepared in deionized water. A volume of 80 μL 1 mol/L HEPES (pH 5.0) was added to 200 μL 68GaCl3 (37-74 MBq) eluent, and then the mixture was incubated with 40 μL DOTA-c(NGR)2 stock solution in a water bath at 95°C for 10 min. Quality control was performed by radio-HPLC (Agilent Technologies, Santa Clara, CA, USA) with a VP-ODS C18 column (Shimadzu, Kyoto, Japan) and an online radioactivity detector (Zonkia Scientific Instruments Co., Ltd., Anhui Province, China). The mobile phase was composed of solvent A, 0.1% trifluoroacetic acid (TFA) in water, and solvent B, 0.1% TFA in acetronitrile. The flow rate was set at 1 mL/min, and the UV wavelength was set at 220 nm. The mobile phase was gradiently changed from 20% solvent B to 30% solvent B in 20 min.

To evaluate the in vitro stability, ~3.7 MBq of 68Ga-DOTA-c(NGR)2 was incubated in phosphate-buffered saline (PBS) at room temperature or bovine serum at 37 °C, respectively. The radiochemical purity was determined at time points of 30 min and 1, 2 and 3 h.

Cell culture and animal model

The human OVCA ES2 and SKOV3 cells were obtained from Nanjing Keygen Biotech Co., Ltd. (Nanjing, China). ES2 cells were maintained as monolayer cultures in McCoy's medium 5A supplemented with 10% fetal bovine serum (FBS), and SKOV3 cells were cultured in RPMI-1640 medium supplemented with 10% FBS. Both cell lines were incubated at 37°C in a humidified atmosphere containing 5% CO2. Cells in log phase were harvested by trypsinization, washed with PBS twice and adjusted to 5×107/mL in PBS. A volume of 0.1 mL single-cell suspension was subcutaneously injected into the front flank of each female BALB/c-neu nude mouse (~4-6 weeks old, body weight of 18-25 g; Slac Laboratory Animal, Shanghai, China). Animal models were used for PET imaging experiments when xenografts grew to 500-1,000 mm3. All animal-related studies were approved by the Institutional Animal Care and Use Committee of Soochow University.

Flow cytometry analysis

ES2 and SKOV3 cells were harvested by trypsinization, washed twice with PBS, and adjusted to a density of 2×105/mL with PBS. The cells were labeled with mouse-anti-human CD13 monoclonal antibody and incubated at 4°C for 30 min, and then the cells were washed with 1 mL cold PBS. Subsequently, the cells were incubated with the secondary antibody labeled with phycoerythrin at 4°C for 30 min. The cells were washed twice and resuspended in 500 μL PBS. Then the labeled cells were analyzed with a flow cytometer (FC-500; Beckman Coulter Inc., Sykesville, MD, USA) to quantify the CD13 expression of OVCA cells.

 Figure 1 

Structural formula of DOTA-c(NGR)2; chemical formula: C99H159N25O41S4; molecular weight: 2,483.74.

J Cancer Image (Click on the image to enlarge.)

Immunohistochemical staining

The xenografted tumors were excised and fixed in 4% buffered formalin (pH 7.0). Sections of paraffin-embedded tumor tissues were baked in an oven at 65°C for 2 h, dewaxed in dimethylbenzene twice, and dehydrated in deionized water and a gradient of alcohol (80%, 95% and 100%). Antigens on the sections were retrieved with antigen repair solution (0.01 M citric acid buffer, pH 6.0), and the endogenous peroxidase activity was eliminated by 3% freshly prepared H2O2. After blocking in 3% BSA (SW3015; Solarbio, Beijing, China) at 37°C for 30 min, the sections were incubated with adequate diluted rabbit anti-CD13 (1:150; Nanjing Keygen Biotech) in a wet box at 4°C for 12 h, followed by the addition of polymeric horseradish peroxidase-labeled rabbit IgG as the secondary antibody. After incubation at 37°C for 30 min and three washes with PBS, sections were stained with a substrate-chromogen solution containing 0.025% 3, 3'-diaminobenzidine for 10 min and counterstained with hematoxylin for 3 min before microscopic observation at low (200×) and high (400×) magnifications.

In vitro cell binding assay

To study the in vitro binding affinity and specificity of 68Ga-DOTA-c(NGR)2 to CD13, ES2 and SKOV3 cells were seeded into 6-well plates at a density of 1×106 cells/well and cultured overnight. Subsequently, 37 KBq 68Ga-DOTA-c(NGR)2 was added into each well, followed by incubation at 37°C for 5, 15, 30 min, 1 and 2 h. Then the supernatant was suctioned, and the cells were washed with PBS for three times and harvested with 0.25% trypsin. Both the supernatant and cell suspension were collected and counted using a gamma counter (CRC-55tR; Capintec, Florham Park, NJ, USA).

Cell-based competitive binding assay was performed with ES2 cells. The cells were incubated with 37 KBq 68Ga-DOTA-c(NGR)2 in the presence of increasing concentrations of unlabeled DOTA-c(NGR)2 (0.2-3.2 μg/mL). After 2 h of incubation at 37°C, the cells were collected and measured using the same method as above-mentioned. The experiments were performed in triplicate. The data were fitted with non-linear regression using GraphPad Prism 7.0 (GraphPad Software, San Diego, CA, USA) to obtain the 50% inhibitory concentration (IC50).

Biodistribution studies

Biodistribution studies were performed using 30 normal ICR (Institute of Cancer Research) mice (18-30 g; age, 4 weeks). At 5, 15, 30, 60 min and 2 h post injection of 3.7 MBq/0.1 mL 68Ga-DOTA-c(NGR)2 via the tail vein, mice (n = 6 per time point) were sacrificed by cervical dislocation. The blood, muscle and other organs of interest (brain, heart, liver, lungs, spleen, pancreas, kidneys, stomach, small intestine and femur) were immediately harvested, weighed and counted with a gamma counter. Data were normalized to the time of injection and expressed as percent injected dose per gram (% ID/g).

MicroPET imaging and blocking experiments

Two groups of female Balb/c nude mice (n=6/group) bearing ES2 tumors were used to conduct static microPET imaging with an Inveon microPET scanner (Siemens Medical Solutions, Erlangen, Germany). The first group was injected with 7.4 MBq 68Ga-DOTA-c(NGR)2 via tail vein under anesthesia with 1%-2% isoflurane, and a series of static image data, 10 min for each time point, were collected at 30 min, 1, 1.5, and 2 h post injection. For blocking studies, the second group of mice was injected with 100 μg unlabeled peptide in 100 μL saline via tail vein, immediately followed by administration of 68Ga-DOTA-c(NGR)2, and then images were acquired at 30 min, 1, 1.5 and 2 h post-injection, each for 10 min. The obtained images were processed using Siemens Inveon Research Workplace 4.0 (IRW 4.0) and reconstructed using three-dimensional ordered-subset expectation maximization. Regions of interest (ROIs) were drawn over the tumor (T) and muscle of the contralateral forelimb, and the latter served as the background (B). Moreover, %ID/g of tumors and the T/B ratio were determined. The same studies were repeated in female Balb/c nude mice bearing SKOV3 tumors without the blocking experiments.

Statistical analysis

All quantitative data were presented as the mean ± standard deviation (SD). Statistical analysis was conducted by one-way analysis of variance and Student's t-test. P < 0.05 was considered statistically significant.


Radiochemistry and stability

Under the condition of bathing at 95°C for 10 min, 68Ga-DOTA-c(NGR)2 was easily prepared with a high labeling rate of 98.01% ± 1.44%, and further purification was not necessary. The retention time of 68Ga-DOTA-c(NGR)2 on radio-HPLC was 4.86 ± 0.27 min (Fig. 2). For the stability study, the radiochemical purity was >96% in saline and >95% in bovine serum after 3 h of incubation (Fig. 3).

Fluorescence-activated cell sorting (FACS) and immunohistochemical staining

FACS revealed that the CD13 expression rates of ES2 cells and SKOV3 cells were 87.2% and 27.6%, respectively (Fig. 4). In accordance with the results of FACS, immunohistochemical staining showed that CD13 was significantly expressed on the membranes of the tumor and endothelial cells of the new vasculature in ES2 tumor tissue, and its expression in ES2 tumor tissue was significantly higher compared with the SKOV3 tumor tissue (Fig. 5).

 Figure 2 

Radio-HPLC of 68Ga-DOTA-c(NGR)2 (retention time was 5.23 min).

J Cancer Image (Click on the image to enlarge.)
 Figure 3 

In vitro stability of 68Ga-DOTA-c(NGR)2 in saline at room temperature and in bovine serum at 37 °C for 30 min, 1 h, 2 h and 3 h.

J Cancer Image (Click on the image to enlarge.)

In vitro cell-binding assay

Cell-binding studies were performed with ES2 cells and SKOV3 cells, and blocking studies were performed with ES2 cells. Significant binding differences were observed between ES2 cells and SKOV3 cells (Fig. 6). The binding of 68Ga-DOTA-c(NGR)2 to ES2 cells was rapid and almost saturated within 30 min, and the highest binding of 3.00% ± 0.59% was achieved after 2 h of incubation, which was significantly higher compared with SKOV3 cells at all time points with a highest binding of 1.79% ± 0.34% (P<0.05) (Fig. 6). Cell-based competitive binding assay demonstrated that the binding of 68Ga-DOTA-c(NGR)2 to ES2 cells was blocked by DOTA-c(NGR)2 in a dose-dependent manner, and the calculated IC50 value was 160.1 nM (Fig. 7).

Biodistribution studies

Figure 8 illustrates the dynamic biodistribution results of 68Ga-DOTA-c(NGR)2 in healthy mice. The highest uptake of the tracer was found in the kidney, which peaked at 5 min (16.7±5.80% ID/g) and then was rapidly decreased by more than 50% at 30 min and 85% at 120 min post-injection. Liver and lung were two other organs with relatively high uptake of the tracer. Quick clearance of 68Ga-DOTA-c(NGR)2 from blood was observed, and the blood uptake was 7.44 ± 1.64% ID/g at 5 min and 0.31 ± 0.05% ID/g at 60 min post-injection. Activities in brain, heart, stomach, intestines, spleen, pancreas and bone were at lower levels.

MicroPET imaging and blocking experiments

Post-intravenous injection with 68Ga-DOTA-c(NGR)2, a series of microPET images of ES2 tumor-bearing mice were collected at 30 min, 1 and 1.5 h and represented by coronal and transverse views (Fig. 9). Significant accumulation of radioactivity in the bladder was observed at all time points. High focal accumulation in tumor was visualized at 1 and 1.5 h, and then it was reduced at 2 h. Quantitative analysis with ROI revealed that the uptake of 68Ga-DOTA-c(NGR)2 in ES2 tumors was 0.62 ± 0.09% ID/g at 1 h and 0.53 ± 0.08% ID/g at 1.5 h, whereas the uptake in SKOV3 tumors at the same time points was 0.32 ± 0.03% ID/g and 0.24 ± 0.05% ID/g, respectively. The T/B ratios in ES2 tumors were 10.30 ± 0.26 at 1 h and 8.04±1.75 at 1.5 h, while such ratios became only 3.99 ± 0.18 at 1 h and 4.24 ± 0.73 at 1.5 h in SKOV3 tumors. The uptake in ES2 tumors was only 0.16 ± 0.03% ID/g at 1 h and 0.14 ± 0.02% ID/g at 1.5 h in the blocking experiment, indicating that the specific targeting of 68Ga-DOTA-c(NGR)2 to the tumor was significantly blocked by the cold peptide.

 Figure 4 

FACS of CD13 expression on ES2 (A) and SKOV3 (B) cells.

J Cancer Image (Click on the image to enlarge.)
 Figure 5 

Immunohistochemical staining. (A) and (B) CD13 expression in SKOV3 tumor tissue sections; (C) and (D) CD13 expression in ES2 tumor cells (black arrows) and tumor vascular endothelia (white arrows). (A and C magnification × 200, B and D magnification ×400).

J Cancer Image (Click on the image to enlarge.)
 Figure 6 

Uptake of 68Ga-DOTA-c(NGR)2 in ES2 and SKOV3 cells.

J Cancer Image (Click on the image to enlarge.)
 Figure 7 

Competitive binding assay. The uptake in ES2 cells could be competitively inhibited by unlabeled DOTA-c(NGR)2 in a dose-dependent manner, and the IC50 value was 160.1 nM.

J Cancer Image (Click on the image to enlarge.)


The effective inhibition of tumor angiogenesis may arrest tumor progression and has shown synergistic effect in other cancer treatments [19, 20]. As one targeted tumor therapy, anti-angiogenic regimen can actually benefit only a few patients due to the biological heterogeneity of tumors [21, 22]. Molecular imaging using radio-labeled tumor-targeting probes can be used to select patients, dynamically assess response to therapy, and therefore predict efficacy of treatment [23]. 68Ga, a generator-based positron radioisotope, is relatively easy to obtain by 68Ge/68Ga radionuclide generators, and it shows high-quality images on PET [24]. CD13 is one of attractive targets of tumorigenic angiogenesis for nuclear imaging. In the present study, we investigated a 68Ga-labeled dimeric cNGR linked by PEG-4 for CD13 specific-targeting PET imaging. Like some previous studies, we employed ES2 cells, which were intensely positive for CD13, and SKOV3 cells, which expressed a low level of CD13, to ensure that the efficacy of 68Ga-DOTA-c(NGR)2 as a new molecular probe that binds to CD13-positive OVCA cells was comparable [9, 10, 25].

68Ga-DOTA-c(NGR)2 with high radiochemical purity was obtained via relatively simple labeling steps without further purification, and the yield remained stable in bovine serum after 3 h. The specificity and cellular binding kinetics of the probe were verified by in vitro experiments with two OVCA cell lines. The potential of 68Ga-DOTA-c(NGR)2 for PET imaging of tumor CD13 expression was also demonstrated by the in vivo experiments with the OVCA model.

 Figure 8 

Biodistribution of 68Ga-DOTA-c(NGR)2 in normal mice (n=6).

J Cancer Image (Click on the image to enlarge.)
 Figure 9 

Representative micro-PET images of 68Ga-DOTA-c(NGR)2 in xenograft models. Dotted circles indicate the tumor regions.

J Cancer Image (Click on the image to enlarge.)

In our previous study, 68Ga-labeled linear NGR conjugated with DOTA, 68Ga-DOTA-NGR, has been synthesized, which shows high selectivity and affinity for CD13 and significant uptake in CD13-positive lung tumors [12]. However, only a few studies have investigated radio-labeled NGR in OVCA. Faintuch et al. have evaluated the uptake of cNGRyk peptide radio-labeled with 99mTc in OVCA cell namely OVCAR-3 and found that the in vivo tumor uptake is pronounced [26]. Meng et al. have synthesized NGR peptide-conjugated Cy5.5 labeled iron oxide (Fe3O4-Cy5.5-NGR) nanoparticles as a targeted NIRF/MR dual-modal imaging nanoprobe and indicated that CD13 can be utilized as a suitable target for OVCA specific imaging [27]. In line with these studies, we observed that the new 68Ga-labeled dimeric cNGR was characterized as a promising diagnostic candidate for OVCA.

In recent years, many inhibitors of APN/CD13 have been designed and synthesized to treat OVCA via reducing the activity and expression of APN/CD13 [9, 10, 28]. However, no relationship has been demonstrated between the expression of CD13 in OVCA and clinical or pathologic variables of the patients [29]. Therefore, the CD13 expression in tumors should be evaluated through biopsy before treatment. However, there are associated risks and contraindications of the biopsy procedure. Moreover, the result is complicated by the heterogeneous spatial expression of CD13 within a tumor. Molecular imaging using radio-labeled peptides can provide a non-invasive means to detect the expressions of special receptors throughout an entire tumor simultaneously, without the need for histological examination [30, 31]. In the present study, a higher uptake of radiotracer was found in ES2 cells compared with SKOV3 cells, indicating that 68Ga-DOTA-c(NGR)2 could be used to evaluate the CD13 expression in OVCA.

It is worth noting that our work is only a preliminary study on the physicochemical and biological characteristics of a newly designed cyclic dimeric probe based on the NGR sequence. It was not compared with other probes of NGR derivatives in previous studies under the same experimental conditions.


A new 68Ga-labeled dimeric cNGR, 68Ga-DOTA-c(NGR)2, was easily synthesized with high radiochemical purity and stability. Both in vitro and in vivo data demonstrated the high selectivity and affinity of 68Ga-DOTA-c(NGR)2 for CD13. Collectively, 68Ga-DOTA-c(NGR)2 might be a potential PET imaging probe for evaluating the CD13 expression in tumor.


68Ga: gallium-68; NGR: asparagine-glycine-arginine; cNGR: cyclic NGR; cNGR2: cyclic NGR dimer; DOTA: 1,4,7,10-tetraazacyclododecane-N,N',N'',N'''-tetraacetic acid; PET: Positron emission tomography; CD13: cluster of differentiation 13; OVCA: ovarian cancer; FBS: fetal bovine serum; % ID/g: percent injected dose per gram; ROI: region of interest; FACS: fluorescence-activated cell sorting.


Ethics approval and consent to participate

All animal studies were performed according to a protocol approved by the Institutional Animal Care and Use Committee of Soochow University (No. 201710A531).


This work was supported by grants from the National Natural Science Foundation of China (No. 6192780137 to Yi Yang; No. 81601522 to Shengming Deng), Natural Science Foundation of Jiangsu Province (No. BK20151352 to Jun Zhang), Young Medical Key Talents Project of Jiangsu Province (No. QNRC2016515 to Jun Zhang; No. QNRC2016749 to Shengming Deng), "Six Ones Project" high-level top medical talent project of Jiangsu Province (No. LGY2017032 to Jun Zhang), the Suzhou Science and Technology Development Plan (No. SYSD2017066 to Yi Yang), the Suzhou New District Science and Technology Plan (No. 2016Z0004 to Yi Yang), and the Suzhou People's Livelihood Science and Technology Project (No. SYS2019038 to Shengming Deng).

Authors' contributions

YY contributed to cell culture and animal experiment, data analysis, and writing of the manuscript. JZ contributed to study design, radio-labeling of peptides, data analysis and interpretation, and writing and critical revision of the manuscript. HZ contributed to micro-PET acquisition and data analysis. YS contributed to flow cytometry analysis, H&E staining, histopathological data acquisition. SD contributed to study design, data analysis, and writing of the manuscript. YW contributed to study design and revision of the manuscript. All authors read and approved the final manuscript.

Competing Interests

The authors have declared that no competing interest exists.


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Author contact

Corresponding address Corresponding authors: Department of Nuclear Medicine, Taizhou People's Hospital, No. 366, Taihu Road, Taizhou, Jiangsu Province, China 225300; E-mail: dr.junzhangcom (Jun Zhang). Department of Nuclear Medicine, the First Affiliated Hospital of Soochow University, No. 188, Shizhi Street, Suzhou, Jiangsu Province, China 215006; E-mail: wuyiwei3988com (Yiwei Wu). Department of Nuclear Medicine, the First Affiliated Hospital of Soochow University, No. 188, Shizhi Street, Suzhou, Jiangsu Province, China 215006; E-mail: dshmingcom (Shengming Deng).

Received 2020-6-17
Accepted 2020-10-24
Published 2021-1-1