Contrast Media & Molecular Imaging

Contrast Media & Molecular Imaging / 2020 / Article
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Research Article | Open Access

Volume 2020 |Article ID 2525037 | 10 pages |

99mTc-CXCR4-L for Imaging of the Chemokine-4 Receptor Associated with Brain Tumor Invasiveness: Biokinetics, Radiation Dosimetry, and Proof of Concept in Humans

Academic Editor: Luděk Šefc
Received15 May 2019
Revised21 Feb 2020
Accepted27 Feb 2020
Published27 Apr 2020


Overexpression of the chemokine-4 receptor (CXCR4) in brain tumors is associated with high cancer cell invasiveness. Recently, we reported the preclinical evaluation of 99mTc-CXCR4-L (cyclo-D-Tyr-D-[NMe]Orn[EDDA-99mTc-6-hydrazinylnicotinyl]-Arg-NaI-Gly) as a SPECT radioligand capable of specifically detecting the CXCR4 protein. This research aimed to estimate the biokinetic behavior and radiation dosimetry of 99mTc-CXCR4-L in healthy subjects, as well as to correlate the radiotracer uptake by brain tumors in patients, with the histological grade of differentiation and CXCR4 expression evaluated by immunohistochemistry. 99mTc-CXCR4-L was obtained from freeze-dried kits prepared under GMP conditions (radiochemical purities >97%). Whole-body scans from six healthy volunteers were acquired at 0.3, 1, 2, 4, 6, and 24 h after 99mTc-CXCR4-L administration (0.37 GBq). Time-activity curves of different source organs were obtained from the image sequence to adjust the biokinetic models. The OLINDA/EXM code was employed to calculate the equivalent and effective radiation doses. Nine patients with evidence of brain tumor injury (6 primaries and 3 recurrent), determined by MRI, underwent cerebral SPECT at 3 h after administration of 99mTc-CXCR4-L (0.74 GBq). Data were expressed as a T/B (tumor uptake/background) ratio. Biopsy examinations included histological grading and anti-CXCR4 immunohistochemistry. Results showed a fast blood activity clearance (T1/2α = 0.81 min and T1/2β = 12.19 min) with renal and hepatobiliary elimination. The average equivalent doses were 6.10E − 04, 1.41E − 04, and 3.13E − 05 mSv/MBq for the intestine, liver, and kidney, respectively. The effective dose was 3.92E − 03 mSv/MBq. SPECT was positive in 7/9 patients diagnosed as grade II oligodendroglioma (two patients), grade IV glioblastoma (two patients), grade IV gliosarcoma (one patient), metastasis, and diffuse astrocytoma with T/B ratios of 1.3, 2.3, 13, 7, 19, 5.5, and 3.9, respectively, all of them with positive immunohistochemistry. A direct relationship between the grade of differentiation and the expression of CXCR4 was found. The two negative SPECT studies showed negative immunohistochemistry with a diagnosis of reactive gliosis. This “proof-of-concept” research warrants further clinical studies to establish the usefulness of 99mTc-CXCR4-L in the diagnosis and prognosis of brain tumors.

1. Introduction

The aggressiveness of high-grade glioblastomas and the refractoriness to conventional therapies are mostly due to their highly invasive nature [1]. Glioblastomas produce many malignant tissue satellites that frequently migrate to substantial distance from the primary tumors, the reason for which they are challenging to eradicate by surgical techniques and chemo- and radiotherapeutic regimens [2, 3].

Previous studies have demonstrated that the overexpression of the chemokine-4 receptor (CXCR4) results in increased migration of glioma tumor cells [4]. This expression is from twenty-five to eighty-nine times higher than that found in noninvasive (low-grade) glioma cells [5]. High expression levels of CXCR4 and its ligand, the chemokine stromal cell-derived factor 1-α (SDF1-α = CXCL12), usually indicate a poor prognosis for patients with brain tumors [6]. Therefore, CXCR4 and CXCL12 are molecular targets of interest for the development of potential targeted cancer therapies.

Recently, a 68Ga-labeled cyclic DOTA-pentapeptide (68Ga-Pentixafor®) was reported as a successful positron emission tomography (PET) tracer, useful for visualization of CXCR4 expression in patients with glioblastoma [7]. Preclinical studies of N-[11C]methyl-AMD3465 PET ligand have also demonstrated the feasibility of obtaining in vivo images of CXCR4 expression in glioma tumors [8]. Both PET tracers might be useful in identifying patients to whom potential CXCR4-targeted radiotherapies (e.g., 177Lu-CXCR4-ligands) could be beneficial [9, 10]. Other CXCR4-ligands for PET and SPECT have also been reported for the detection of CXCR4 expression in different tumors, but only at a preclinical stage [1114]. 68Ga-Pentixafor® is the only CXCR4-ligand used in clinical protocols.

Our group recently reported the synthesis, formulation, and preclinical evaluation of 99mTc-CXCR4-L (cyclo-D-Tyr-D-[NMe]Orn[EDDA-99mTc-6-hydrazinylnicotinyl]-Arg-NaI-Gly) as a SPECT radioligand capable of specifically detecting the CXCR4 protein [9].

This research aimed to estimate the biokinetic behavior and radiation dosimetry of 99mTc-CXCR4-L in healthy subjects, as well as to correlate the radiotracer uptake by brain tumors in patients, with the histological grade of differentiation and CXCR4 expression evaluated by immunohistochemistry.

2. Materials and Methods

2.1. Reagents

A CXCR4-L (cyclo-D-Tyr-D-[NMe]Orn[6-hydrazinylnicotinyl]-Arg-NaI-Gly, MW 837 g/mol) freeze-dried kit formulation was obtained from the “Instituto Nacional de Investigaciones Nucleares” (ININ, Mexico) prepared under GMP conditions [9]. 99mTcO4Na was obtained from a GETEC 99Mo/99mTc generator (ININ, Mexico). All the other reagents were used as received from Sigma-Aldrich Chemical Co.

2.2. Preparation of 99mTc-CXCR4-L

Technetium-99m-labeled CXCR4-L (99mTc-CXCR4-L) was prepared according to the supplier’s instructions [9]. In brief, radiolabeling was achieved by adding 1 mL of 0.2 M phosphate buffer (pH 7.0) solution to the CXCR4-L lyophilized formulation (GMP-grade, ININ-México) with immediate addition of 0.37–0.74 GBq (1 mL) of 99mTcO4Na eluant and incubation at 95°C in a dry bath (heating block) for 10 min. The radiochemical purities of 99mTc-CXCR4-L were assessed by reverse-phase radio-HPLC as reported by Avila-Sanchez et al. [9].

2.3. Healthy Subjects and Patients

Six healthy subjects (age range: 28–37 y; mean age ± SD: 33 ± 4 y; 3 females and 3 males) were included. Physical examination and medical history were performed. Individuals with a history of major surgery (e.g., organ removal) or evidence of clinical disease were excluded. Mean (±SD) subject weight was 62 ± 10 kg (range, 51–76 kg). After receiving full information concerning the aims of the study, all volunteers agreed to participate in the complete biokinetic study and signed a consent form. The activity administered to healthy subjects was 0.37 GBq (25 μg of CXCR4-L peptide).

Nine patients between 25 and 72 y (mean age ± SD: 42 ± 16 y), with evidence of brain tumor injury (6 with an indeterminate brain tumor and 3 with suspicion of tumor recurrence), established by magnetic resonance imaging (MRI) studies, were included in the study (Table 1). This research was carried out at the Nuclear Medicine Department at the Specialties Hospital of “Centro Médico Nacional Siglo XXI, Instituto Mexicano del Seguro Social,” Mexico. Informed consent was given by the patients, and the protocol was approved by the institutional ethics committee, considering the following aspects: (a) Helsinki Declaration (1975; revised version, 2008) and the ethical standards of the institutional committee related to human experimentation, (b) the GMP certificate granted to ININ by COFEPRIS (“Comisión Federal para la Protección contra Riesgos Sanitarios”: regulatory authority in Mexico), (c) the complete preclinical studies of 99mTc-CXCR4-L, and (d) the basis of “proof-of-concept” and microdosing studies.

Target organN (mean ± SD) (MBq·h/MBq)

Breasts(1.39 ± 0.30) E − 01
Gallbladder content(3.07 ± 1.30) E − 02(1.33 ± 0.09) E − 02
LLI content(6.46 ± 1.27) E − 02(7.27 ± 0.40) E − 02
SI content(1.01 ± 0.20) E − 01(1.14 ± 0.06) E − 01
ULI content(1.32 ± 0.26) E − 01(1.48 ± 0.08) E − 01
Heart content(2.96 ± 0.18) E − 02(3.68 ± 0.75) E − 02
Kidneys(1.01 ± 0.20) E − 01(1.46 ± 0.20) E − 01
Liver(1.23 ± 0.41) E − 01(1.66 ± 0.25) E − 01
Lungs(1.70 ± 0.38) E − 01(2.41 ± 0.40) E − 01
Testes(2.53 ± 0.09) E − 02
Urinary bladder(2.48 ± 0.40) E − 01(1.70 ± 0.45) E − 01
Remainder of the body1.13 ± 0.081.83 ± 0.04

2.4. Acquisition of Images

99mTc-CXCR4-L images in volunteers were obtained with a Symbia TruePoint dual-head gamma camera (SPECT/CT, Siemens), with high-resolution and low-energy collimators. The established parameters were velocity: 12 cm/min; matrix size: 256 × 1024 pixels; window: 20% symmetric at 140 keV; and scatter corrections: dual-energy window with simultaneous acquisition at 119 keV (20% width). Transmission factors to obtain the body (abdomen and chest) attenuation were calculated by using the I/I0 counting rate, with (I) and without (I0) the patient of a 99mTc-filled flood source (555 MBq). Anterior and posterior scintigraphy of the whole body was obtained at 0.3, 1, 2, 4, 6, and 24 h after radiopharmaceutical administration.

In patients, preoperative (15 ± 5 d before surgery) cerebral SPECT (Siemens E. Cam Signature double detector) images were acquired at 3 h after 99mTc-CXCR4-L (0.74 GBq) administration using a 128 × 128 matrix, window centered on 140 keV, with scattering correction, 360-degree rotation, 128 images of 20 s, and a total duration of approximately 21 min.

2.5. Image Analysis

Visual and semiquantitative analyses were performed by two physicians (specialized in nuclear medicine and molecular imaging) with an experience of >9 years in the use of the Siemens Syngo Acquisition Workplace equipment workstation with processing software for volumetric analysis. The tumor/background (T/Bmax) uptake ratio was calculated by quantifying the number of maximum counts obtained by delimiting volumetric regions (3D) of interest (VOI) with the isocontour around the entire tumor area (T) and in the contralateral brain region (B).

2.6. Biokinetic Evaluation

Images obtained in the DICOM (Digital Imaging and Communication in Medicine) format were processed using ImageJ Software (V1.51i, in Java, Image Processing and Analysis) for scattering correction by using the dual-energy window method. By using the transmission factors (I/I0) experimentally calculated as described above, regions of interest of source organs (liver, bladder, heart, spleen, intestine, lungs, kidneys, and whole-body) were corrected by attenuation. The activity in each source organ was divided by the initial whole-body (WB) activity (100% of injected activity) to determine the injected activity fraction (IA):

Technetium-99m time-activity curves were built from the image sequence in each organ. As the heart does not overexpress CXCR4, its activity was considered as having blood activity kinetics. The % IA data at different times were used in the OLINDA/EXM code to calculate the total number of disintegrations (N, MBq.h/MBq). The GI tract model (ICRP 30) included in the code was employed for the excretion model considering an activity fraction of 0.061–0.027 entering the small intestine, as images showed that 4.42 ± 1.69% of the 99mTc-CXCR4-L injected activity is excreted to the intestine at 20 min after administration (Tables S1S6, supplementary material). % IA in urine (bladder activity) was also considered as excretion data in the OLINDA code.

2.7. 99mTc-CXCR4-L Absorbed Dose

Equivalent doses were evaluated according to general equation (2), as previously reported [15]:where is the radiation absorbed, is the total number of disintegrations, and is the absorbed dose per nuclear transition. The equivalent and effective radiation doses were obtained by using the experimental N values in the OLINDA/EXM code [15].

2.8. Tumor Tissue Samples

All patients underwent total or partial tumor resection. Histopathology was the gold standard to verify the diagnosis as well as to determine the presence of viable tumor tissue. The histopathological reports were collected by the Pathology Department of the “Hospital de Especialidades of CMN Siglo XXI, IMSS,” which were interpreted by a certified and experienced pathologist according to the World Health Organization (WHO) classification for tumors of the central nervous system (2016): high-grade gliomas (HGG) III-IV, low-grade gliomas (LGG) I-II, and metastasis.

2.9. Immunohistochemical Studies

Immunohistochemical staining of tumor specimens was carried out by using a human anti-CXCR4 monoclonal antibody (1 : 1000 dilution, MAB172, R&D Systems) with BOND equipment (Leica Biosystems). The analysis was performed double-blind by two pathologists, which selected five random fields for each tumor specimen under an optical microscope (magnification 200x). Gastric cancer tissue was used as an internal positive control for the expression of CXCR4.

2.10. Statistical Analysis

To analyze the relationship between the pathological grade (WHO classification) and the brain tumor uptake evaluated by SPECT (T/Bmax ratio), nonparametric tests were used.

3. Results and Discussion

The radiochemical purity of 99mTc-CXCR4-L (Figure 1), obtained from the freeze-dried kits, was 98 ± 1%, as obtained by HPLC analyses. The average molar activity was 13 GBq/μmol before injection to patients.

None of the healthy volunteers reported adverse reactions such as bradycardia, itching, hives, vomiting, nausea, flushing, bronchospasm, dyspnea, coughing, chills, decreased blood pressure, or dizziness after 99mTc-CXCR4-L administration.

The 99mTc-CXCR4-L blood activity biokinetic model is shown in the following equation:

The half-life value was 0.0136 h (0.81 min) for the fast component (T1/2α = ln 2/51.01), 0.203 h (12.19 min) for the first slow component (T1/2β = ln 2/3.41), and 2.03 h for the second slow component (T1/2γ = ln 2/0.34) (Figure 2). The activity was rapidly eliminated by kidneys and the hepatobiliary system (Figure 3). The activity in the kidneys at 20 min was 4.28 ± 1.43%, and after 24 h, it decreased to 0.10 ± 0.07%. Twenty-four hours after the administration of 99mTc-CXCR4-L, the total activity excreted from the whole body was 99.18 ± 0.24% (Supplementary Material, Tables S1S6).

The total disintegrations that occurred in each organ are shown in Table 1, and the equivalent doses of 99mTc-CXCR4-L for the main source organs are shown in Table 2. Due to the fast radiopharmaceutical elimination, the effective dose of 99mTc-CXCR4-L (2.67–3.14 mSv/740 MBq) is in the same order of magnitude than that reported for other 99mTc peptides, such as 99mTc-RGD (6.1 mSv/740 MBq) or 99mTc-iPSMA (3.42 mSv/740 MBq) [16, 17], and below 10 mSv, in agreement with the recommendation of the World Health Organization [18].

Target organEquivalent doses (mean ± SD) (mSv/MBq)

Adrenals(8.93 ± 1.31) E − 06(8.38 ± 2.27) E − 06
Brain(3.32 ± 0.25) E − 06(3.54 ± 0.96) E − 06
Breasts(3.02 ± 0.64) E − 04(4.70 ± 0.26) E − 05
Gallbladder wall(1.59 ± 0.48) E − 04(1.00 ± 0.04) E − 04
LLI wall(6.10 ± 0.64) E − 04(6.10 ± 0.30) E − 04
Small intestine(2.05 ± 0.21) E − 05(1.71 ± 0.50) E − 05
Stomach wall(1.87 ± 0.14) E − 04(2.01 ± 0.47) E − 04
ULI wall(3.30 ± 0.45) E − 05(2.74 ± 0.80) E − 05
Heart wall(5.26 ± 0.64) E − 05(5.57 ± 0.53) E − 05
Kidneys(3.13 ± 0.57) E − 05(1.03 ± 0.89) E − 04
Liver(1.41 ± 0.36) E − 04(1.46 ± 0.16) E − 04
Lungs(4.37 ± 0.90) E − 04(4.71 ± 0.57) E − 04
Muscle(5.81 ± 0.46) E − 06(5.41 ± 1.56) E − 06
Ovaries(5.63 ± 0.16) E − 04(0.00 ± 0.00) E+00
Pancreas(9.13 ± 0.12) E − 06(8.35 ± 2.29) E − 06
Red marrow(1.46 ± 0.01) E − 04(1.67 ± 0.05) E − 04
Osteogenic cells(2.68 ± 0.22) E − 05(3.18 ± 0.09) E − 05
Skin(6.57 ± 0.59) E − 06(7.67 ± 0.25) E − 06
Spleen(7.35 ± 0.80) E − 06(7.02 ± 1.84) E − 06
Testes(0.00 ± 0.00) E+00(1.75 ± 0.07) E − 03
Thymus(6.22 ± 0.77) E − 06(5.63 ± 1.70) E − 06
Thyroid(3.88 ± 0.36) E − 05(5.45 ± 0.16) E − 05
Urinary bladder wall(7.76 ± 1.15) E − 04(4.06 ± 0.90) E − 04
Uterus(1.52 ± 0.06) E − 05(1.15 ± 0.38) E − 05
Effective dose (mSv/MBq)(3.59 ± 0.29) E − 03(4.24 ± 0.21) E − 03

Table 3 shows the T/Bmax ratios calculated using SPECT images from patients. Histopathological studies confirmed 3 HGG (1 gliosarcoma and 2 GBM), 2 LGG (oligodendroglioma), 1 metastasis (poorly differentiated carcinoma), 1 recurrent glioma (astrocytoma II), and 2 reactive glioses (see images in the Supplementary Material section). Among the 6 cases with an undetermined brain tumor, SPECT was positive in 3 HGG (T/Bmax 10.8 ± 5.7), 2 LGG (T/Bmax 1.8 ± 0.5), and 1 brain metastasis (T/Bmax 5.5). Of the patients with suspicion of tumor recurrence, SPECT was positive in one (diffuse astrocytoma II) with T/Bmax 3.9 (Figure 4), while for the rest, the result was negative, with a histological report of reactive gliosis. T/Bmax significantly correlated with the pathological grade (WHO classification) (Spearman rs = 0.94, ) (Figure 5).

Patient no.AgeReported diseaseWHO gradeT/Bmax ratio

130Oligodendroglioma NOSII1.3
244Oligodendroglioma NOSII2.4
342Glioblastoma NOSIV6.6
472Glioblastoma NOSIV7
651Metastasis of poorly differentiated malignancyNA5.5
725Diffuse astrocytoma NOS (tumor recurrence)II3.9
825Reactive gliosis (tumor recurrence)NANA
934Reactive gliosis (tumor recurrence)NANA

Immunohistochemical results corroborated that CXCR4 was highly expressed in HGG, whereas its expression in LGG was very low and absent in reactive gliosis (Figure 6). As it is known, CXCR4 is overexpressed in various tumors, including HGG and brain metastasis, involved in the tumor growth, angiogenesis, recurrence, resistance to therapy, shorter survival, and poor conditioning prognosis [6]. In agreement with the results of this research, it has been reported that primary brain tumor cell lines have high concentrations of CXCR4 compared to the normal brain parenchyma, demonstrating CXCR4 overexpression of up to 81% in glioblastoma tumor tissues [19, 20]. In this context, Lapa et al. [7] used 68Ga-Pentixafor for glioblastoma PET imaging in 15 patients and compared it with 18F-FET (O-(2-18F-fluoroethyl)-L-tyrosine). They reported higher tumor/background ratios in the 68Ga images compared to those of 18F, as well as good retention in the tumor lesion. In this research, the use of SPECT with 99mTc-CXCR4-L in patients with suspected brain tumors demonstrated a specific tumor uptake, which allowed adequate discrimination between tumor recurrence and gliosis. Likewise, the absence of intraparenchymal concentration permitted to obtain images for clinical use with appropriate T/Bmax ratios (HGG 10.8 ± 5.7, LGG 1.8 ± 0.5, and cerebral metastasis 5.5). The immunohistochemical confirmation of higher CXCR4 expression in patients with HGG with regard to those with LGG corroborated the directly proportional relationship between the grade of differentiation and the expression of CXCR4. This “proof-of-concept” research showed the potential utility of 99mTc-CXCR4-L in the specific diagnosis and prognosis of brain tumors.

4. Conclusions

The equivalent and effective radiation doses of 99mTc-CXCR4-L in humans are comparable to those from most diagnostic studies of 99mTc. This preliminary study warrants further clinical studies in order to establish the usefulness of 99mTc-CXCR4-L in the diagnosis, prognosis, prediction of therapeutic response, discrimination between recurrence, and reactive gliosis, as well as in the selection of patients who could benefit from targeted anti-CXCR4 therapies.

Data Availability

The data used to support the findings of this study are included within the article.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.


This research was completed as part of the activities of the Laboratorio Nacional de Investigación y Desarrollo de Radiofármacos, CONACyT-Mexico. This study was supported by the Mexican National Council of Science and Technology (CONACYT, Grant 242443).

Supplementary Materials

In the supplementary material section, the whole-body images of healthy volunteers, including the tables of corrected counts, the percentage of injected activity (% IA) per organ at different times, and OLINDA calculations are presented. The cerebral SPECT images of all patients involved in this study are also included. 1. Whole-body images of healthy subjects (volunteers), tables of corrected counts, and % IA. 2. Example of the dose assessment: healthy subject 3 (female). 3. Example of the dose assessment: healthy subject 4 (male). (Supplementary Materials)


  1. V. N. Yadav, D. Zamler, G. J. Baker et al., “CXCR4 increases in-vivo glioma perivascular invasion, and reduces radiation induced apoptosis: a genetic knockdown study,” Oncotarget, vol. 7, pp. 83701–83719, 2016. View at: Publisher Site | Google Scholar
  2. F. Gagliardi, A. Narayanan, M. Reni et al., “The role of CXCR4 in highly malignant human gliomas biology: current knowledge and future directions,” Glia, vol. 62, no. 7, pp. 1015–1023, 2014. View at: Publisher Site | Google Scholar
  3. M. Ehtesham, X. Yuan, P. Kabos et al., “Glioma tropic neural stem cells consist of astrocytic precursors and their migratory capacity is mediated by CXCR4,” Neoplasia, vol. 6, no. 3, pp. 287–293, 2004. View at: Publisher Site | Google Scholar
  4. J. M. Munson, R. V. Bellamkonda, and M. A. Swartz, “Interstitial flow in a 3D microenvironment increases glioma invasion by a CXCR4-dependent mechanism,” Cancer Research, vol. 73, no. 5, pp. 1536–1546, 2012. View at: Publisher Site | Google Scholar
  5. M. Ehtesham, J. A. Winston, P. Kabos, and R. C. Thompson, “CXCR4 expression mediates glioma cell invasiveness,” Oncogene, vol. 25, no. 19, pp. 2801–2806, 2006. View at: Publisher Site | Google Scholar
  6. M. Ehtesham, E. Min, N. M. Issar, R. A. Kasl, I. S. Khan, and R. C. Thompson, “The role of the CXCR4 cell surface chemokine receptor in glioma biology,” Journal of Neuro-Oncology, vol. 113, no. 2, pp. 153–162, 2013. View at: Publisher Site | Google Scholar
  7. C. Lapa, K. Lückerath, I. Kleinlein et al., “68Ga-pentixafor-PET/CT for imaging of chemokine receptor 4 expression in glioblastoma,” Theranostics, vol. 6, no. 3, pp. 428–434, 2016. View at: Publisher Site | Google Scholar
  8. S. V. Hartimath, A. van Waarde, R. A. J. O. Dierckx, and E. F. J. de Vries, “Evaluation of N-[11C]Methyl-AMD3465 as a PET tracer for imaging of CXCR4 receptor expression in a C6 glioma tumor model,” Molecular Pharmaceutics, vol. 11, no. 11, pp. 3810–3817, 2014. View at: Publisher Site | Google Scholar
  9. M. Avila-Sanchez, G. Ferro-Flores, N. Jimenez-Mancilla et al., “Synthesis and evaluation of the 99mTc-/177Lu-CXCR4-L theranostic pair for in-vivo targeting of the chemokine-4 receptor,” Journal of Radioanalytical and Nuclear Chemistry, 2019, In press. View at: Publisher Site | Google Scholar
  10. M. Schottelius, T. Osl, A. Poschenrieder et al., “[177Lu]pentixather: comprehensive preclinical characterization of a first CXCR4-directed endoradiotherapeutic agent,” Theranostics, vol. 7, no. 9, pp. 2350–2362, 2017. View at: Publisher Site | Google Scholar
  11. Y. H. Oum, D. Shetty, Y. Yoon et al., “A benzenesulfonamide derivative as a novel PET radioligand for CXCR4,” Bioorganic & Medicinal Chemistry, vol. 28, no. 2, Article ID 115240, 2020. View at: Publisher Site | Google Scholar
  12. A. Amor-Coarasa, J. M. Kelly, P. K. Singh et al., “[18F]Fluoroethyltriazolyl monocyclam derivatives as imaging probes for the chemokine receptor CXCR4,” Molecules, vol. 24, no. 8, p. E1612, 2019. View at: Publisher Site | Google Scholar
  13. A. Amor-Coarasa, J. Kelly, S. Ponnala et al., “[18F]RPS-544: a PET tracer for imaging the chemokine receptor CXCR4,” Nuclear Medicine and Biology, vol. 60, pp. 37–44, 2018. View at: Publisher Site | Google Scholar
  14. A. Mikaeili, M. Erfani, and O. Sabzevari, “Synthesis and evaluation of a 99mTc-labeled chemokine receptor antagonist peptide for imaging of chemokine receptor expressing tumors,” Nuclear Medicine and Biology, vol. 54, pp. 10–17, 2017. View at: Publisher Site | Google Scholar
  15. M. G. Stabin, R. B. Sparks, and E. Crowe, “OLINDA/EXM: the second-generation personal computer software for internal dose assessment in nuclear medicine,” The Journal of Nuclear Medicine, vol. 46, pp. 1023–1027, 2005. View at: Google Scholar
  16. Z. Ortiz-Arzate, C. L. Santos-Cuevas, B. E. Ocampo-García et al., “Kit preparation and biokinetics in women of 99mTc-EDDA/HYNIC-E-[c(RGDfK)]2 for breast cancer imaging,” Nuclear Medicine Communications, vol. 35, no. 4, pp. 423–432, 2014. View at: Publisher Site | Google Scholar
  17. C. Santos-Cuevas, J. Davanzo, G. Ferro-Flores et al., “99mTc-labeled PSMA inhibitor: biokinetics and radiation dosimetry in healthy subjects and imaging of prostate cancer tumors in patients,” Nuclear Medicine and Biology, vol. 52, pp. 1–6, 2017. View at: Publisher Site | Google Scholar
  18. World Health Organization, “Technical report series 611: use of ionizing radiation and radionuclides on human beings for medical research, training, and nonmedical purposes,” Tech. Rep., World Health Organization, Geneva, Switzerland, 1977. View at: Google Scholar
  19. Y. Zhou, P. H. Larsen, C. Hao, and V. W. Yong, “CXCR4 is a major chemokine receptor on glioma cells and mediates their survival,” Journal of Biological Chemistry, vol. 277, no. 51, pp. 49481–49487, 2002. View at: Publisher Site | Google Scholar
  20. C.-C. Wang, D.-Y. Hueng, A.-F. Huang et al., “CD164 regulates proliferation, progression, and invasion of human glioblastoma cells,” Oncotarget, vol. 10, pp. 2041–2054, 2019. View at: Publisher Site | Google Scholar

Copyright © 2020 Paola Vallejo-Armenta 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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