Introduction

Colorectal cancer (CRC) is one of the most commonly diagnosed cancers worldwide, accounting for 10% of all malignancies1,2. Despite advancement in CRC treatment, liver metastasis remains a great obstacle in effective CRC treatment3,4. Up to 25% of patients with primary CRC present with synchronous colorectal liver metastases (CLM) at initial diagnosis, and 50% of patients develop metachronous CLM within 3 years following resection of the primary lesion5,6. Liver metastasis is a more important risk factor for survival than the primary CRC itself7. Therefore, early detection of CLM is of critical medical interest.

Positron emission tomography (PET) is a non-invasive imaging method that facilitates imaging of the whole tumor and is a promising method to analyze intratumoral heterogeneity8,9. Of note, 18F-fluorodeoxyglucose (18F-FDG) and 18F-fluoromisonidazole (18F-FMISO) PET is becoming increasingly popular to monitor the biological behavior of tumors, including glucose metabolism, cell proliferation, and hypoxic response10,11,12. 18F-FDG is a glucose analogue that can be transported into cells by glucose transporters, where it is phosphorylated to 18F-FDG-6-phosphate which cannot undergo further metabolism and remains trapped in the cells. Increased glycolysis or energy metabolism in tumor cells results in an enhancement of 18F-FDG uptake and accumulation, an index of tumor growth and development13,14. Whereas, 18F-FMISO could selectively bind to hypoxic cells, serving as an assessment of hypoxic response in human cancers. 18F-FDG/18F-FMISO-based PET imaging is used in tumor staging and follow-up examination of multiple malignancies including glioblastoma15, head and neck cancer16, lung cancer17, breast cancer18, and CRC19. Nevertheless, these radiotracers have not been applied to monitor CLM yet.

This study aimed to investigate whether 18F-FDG- and 18F-FMISO-based PET can be used to monitor the CLM derived from the CRC cell lines LoVo and HT29, which have different metastatic potentials, by assessing the correlation between radiotracer uptake and tumor marker expression in vitro and in vivo.

Methods

Synthesis of 18F-FDG and 18F-FMISO

18F-FDG and 18F-FMISO were synthesized using a multi-functional module (purity >95%, WuXi Jiangyuan Industrial Technology and Trade Corporation) as previously described20. The 18F-labeled tracers were formulated in normal saline and passed through a 0.22 μm Millipore filter (Millipore, Billerica, MA, USA) for administration to animals.

Cell culture

The human CRC cell lines LoVo and HT29 were purchased from the Type Culture Collection of the Chinese Academy of Sciences, Shanghai, China, and were maintained in Dulbecco’s Modified Eagle Medium (DMEM; Gibco Corporation, USA) and McCoy’s 5 A medium (Gibco), respectively. The culture media were supplemented with 10% fetal bovine serum (FBS; Hyclone, USA) and 1% penicillin-streptomycin in a humidified atmosphere of 5% CO2 at 37 °C. To induce hypoxic response and starvation, the cells were cultured in a humidified atmosphere of 1% O2, 5% CO2 and 94% N2 at 37 °C for 24 h and free-serum starved at 37 °C for 12 h, respectively.

CLM model

Forty 5-week-old female BALA/C nude mice weighing 16–18 g were purchased from the Animal Laboratory of Cavens Corporate of Changzhou (Changzhou, Jiangsu, China). The mice were maintained and used according to the institutional guidelines of Jiangsu Institute of Nuclear Medicine Animal Care and Use Committee (IACUC). All animal experiments were conducted in compliance with the protocols approved by the Institutional Animal Care and Use Committee (IACUC) of Jiangsu Institute of Nuclear Medicine. All mice were acclimatized for three days and then injected under general anesthesia (2% isoflurane in pure O2) with 5.0 × 106 LoVo or HT29 cells (20 mice for each cell line) in 0.15 mL of phosphate-buffered saline (PBS) into the spleens. After injection, body weight was recorded every 3 days.

Wound healing assay

LoVo or HT29 cells were seeded in 6-well plates at 5 × 105 cells/ml and were cultured until 90% confluency. The cells were scratched with a 10 μL pipette tip to create a wound, followed by imaging (0 h). The cells were then treated with 2% FBS-containing medium and imaged (Olympus, Japan) 24 and 48 h after scratching. The wounded area was measured using the Image J software (NIH, Bethesda, MD, USA). Wound healing was determined using the following formula: wound healing% = (wounded area at 0 h-wounded area at indicated time)/wounded area at 0 h × 100%.

Cell invasion assay

The cell invasion assay was performed in 24-well Transwell chambers (Corning, Costar, USA)21. The upper chambers of the Transwell plates were coated with 20 μL of Matrigel matrix (Corning, 356234, USA) diluted in serum-free DMEM (1:40) and incubated at 37 °C for 1 h. The cells (100 μL, 2 × 104 cells/mL) in serum-free DMEM were added to the upper chamber. Complete medium (500 μL) containing 10% FBS was added to the lower chamber as chemo-attractant. After incubation for 72 h, non-invading cells on the surface of the upper chamber were removed with a cotton swab. The invading cells on the lower membrane were fixed with formaldehyde and stained with Giemsa (G1010, Solarbio, China). The images were taken under an Olympus BX53 microscope at 40× magnification (Olympus, Japan). The cells were counted using the Image J software (NIH).

In vitro cellular uptake of radiotracers

The LoVo and HT29 cells were cultured at 37 °C in a hypoxic atmosphere of 1% O2 for 24 h prior to 18F-FMISO uptake or in corresponding serum-free medium at 37 °C atmosphere of 5% CO2 for 12 h prior to 18F-FDG uptake. The cell density was adjusted to 5 × 105 cells/100 µl. For the X group, 100 µl of cell suspension were incubated with the same volume of radiotracer (18F-FDG or 18F-FMISO) and buffer (DMEM containing 0.2% bovine serum albumin) in a glass tube at 37 °C for 30, 60, 120 and 240 min. The mixture of 100 μl of radiotracer and 200 μl of buffer was used as a control group (the O group). A volume of 100 μl of radiotracer was used to measure the radiotracer doses (the T group). After incubation, the O and X groups were centrifuged at 1000 rpm/min for 5 min and the supernatants were removed. The radioactivity was measured using a PerkinElmer 2480 automatic gamma counter (Waltham, MA, USA). The ratio of cellular radionuclide uptake was calculated using the following formula: X(cpm)-O(cpm)/T(cpm)%. cpm: counts per minute. The experiments were independently repeated three times.

Micro-PET imaging

18F-FDG/18F-FMISO-based PET imaging was performed 7 weeks after the injection of tumor cells. The mice were fasted but allowed access to drinking water for 12 h, followed by administration of 18F-FDG. 18F-FDG and 18F-FMISO injections were performed on separate days, 48 h apart. Ten-minute static 18F-FDG (3.7 MBq, 100 μCi) and 18F-FMISO (14.8 MBq, 400 μCi) PET images were acquired at 1 and 4 h after injection via the tail vein under isoflurane anesthesia, in a 3-dimensional mode using an Inveon micro-PET scanner (Siemens Medical Solutions, Erlangen, Germany). Body temperature of the mice was maintained using a heat lamp. PET images were reconstructed using the Inveon Acquisition Workplace software (version 2.0, Siemens Preclinical Solutions) and an ordered-subset expectation maximization method with the following parameters: matrix, 128 × 128 × 159; voxel size, 0.86 × 0.86 × 0.8 mm; β-value, 1.5, with uniform resolution. The regions of interest (ROI) were drawn on images around the entire liver metastastic lesions using the ASI Pro VM 6.8.6.9 software (Concorde Microsystems, Knoxville, TN, USA). For the semi-quantitative evaluation of 18F-FDG or 18F-FMISO uptake in the liver metastasis lesions, the highest and the average tracer concentrations were determined as a maximum/mean standardized uptake value (SUVmax/mean) calculated as: SUVmax/mean = [Max/Mean × 8000μCi/ml × weight(g)]/Injected dose μCi. The liver metastasis were confirmed by visualization post anatomy.

Immunofluorescence assay

LoVo and HT29 cells were plated on sterile slides in 6-well plates and cultured in a modular incubator chamber at 37 °C in a hypoxic atmosphere of 1% O2 for 24 h prior to staining of HIF-1α and were serum-starved for 12 h prior to staining of glucose transporter 1 (GLUT-1). Cells were washed with PBS three times and fixed with 4% paraformaldehyde for 30 min at room temperature, followed by incubation with 1% Triton X-100 for 15 min at room temperature. Following 30 min of blocking with 10% normal goat serum, the cells were incubated with anti-HIF-1α (1:100; H1alpha67; Abcam, UK) or anti-GLUT-1 (1:100; ab40084; Abcam, UK)22. Images were taken with a confocal microscope (C2si; Nikon, Japan). The protein expression was quantified using the Live Cell Imaging System (NIS-Elements, Japan).

Immunohistochemical staining

The liver metastasis specimens of the xenografts were fixed in 10% formalin for 48 h, paraffin-embedded, and cut into 3-μm-thick sections. Immunohistochemical staining was performed as previously described23. Briefly, the slides were incubated with anti-HIF-1α (1:100; Abcam) or anti-GLUT-1 (1:100; Abcam) overnight at 4 °C. The slides were incubated with HRP-labeled goat anti-mouse secondary antibody (Boster, Wuhan, China) for 1 h at room temperature followed by counterstaining with hematoxylin. The staining was observed under a BX53 Olympus microscope (Olympus) at magnification 200×. The brown-yellow staining levels of the HIF-1α and GLUT-1 proteins were evaluated using the Image J software (NIH, Bethesda, MD, USA) and expressed as mean optical density.

Western blot

Western blot experiments were performed as previously described24. Tumor tissues were lysed in RIPA buffer for 30 min at 4 °C. Protein concentrations were determined using a bicinchoninic acid kit (Beyotime Biotech, China). Equivalent amounts of protein were resolved in 10% or 12% SDS-PAGE gel and transferred to polyvinylidene fluoride membranes (Millipore). The membranes were blocked with 10% non-fat dry milk in TRIS-buffered saline containing 0.1% tween-20 for 1 h, and incubated with anti-HIF-1α (1:1000; Abcam), anti-GLUT-1 (1:1000; Abcam), or anti-GAPDH (1:5000; ZhongShan Golden Bridge Biotech Co., China) overnight at 4 °C, followed by additional incubation with peroxidase-conjugated secondary antibody (1:5000; ZhongShan Golden Bridge Biotech Co., China) for 1 h at room temperature. The bands were detected using a Bio-Rad chemiDoc XRS + imaging system (Bio-Rad, Hercules, CA, USA) and quantified using Image J (NIH) by normalization to GAPDH.

Statistical analysis

All data were expressed as means ± standard deviation. Statistical analysis was performed using SPSS version 19 (IBM, Armonk, NY, USA). The differences between the two groups were assessed using the Student’s unpaired t-test. The differences in liver metastatic potential were compared by the Fisher exact test. The correlations were analyzed using linear regression. A P value < 0.05 was considered statistically significant.

Results

LoVo cells are more prone to metastasis than HT29 cells in vivo

To evaluate the metastatic potential of CRC cells in vivo, we established two xenograft models using LoVo and HT29 cells, and compared the ratio of liver metastases between these two models. Liver metastases were confirmed by pathological examination. The percentage of liver metastases was defined as the number of mice with liver metastasis in a group divided by the total number of mice in the group. The percentage of liver metastases with LoVo cells was significantly higher than with HT29 cells (10/20, 50% vs. 4/20, 20%, P = 0.048). The median survival of LoVo-CLM mice was significantly shorter than that of the HT29-xenografted ones (8.5 weeks vs. 10.5 weeks, P < 0.01; Fig. 1). These data suggest that LoVo cells exhibit a stronger metastatic potential than HT29 cells.

Figure 1
figure 1

Survival curves of the LoVo and HT29 xenograft models. **P < 0.01; n = 20.

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Comparison of in vivo radiotracer uptake between LoVo and HT29 CLM

We next sought to investigate whether radiotracer uptake could serve as an indicator of CRC metastasis. To evaluate and compare the abilities of radiotracer uptake in vivo between LoVo and HT29 xenografts, we performed a 18F-FDG PET/18F-FMISO-based Micro-PET analysis using metastatic liver tissues from LoVo and HT29 CLMs, respectively. The timeline of PET imaging is shown in Fig. 2B. The location of liver and tumor tissues in PET imaging were corresponded with the anatomical location. Liver metastasis >0.5 cm could be detected in 18F-FDG PET/18F-FMISO-based micro-PET images. The images of 18F-FDG PET and 18F-FMISO PET as well as the images of liver metastases from LoVo or HT29 xenograft models are shown in Fig. 2A. The SUVmax and SUVmean values of 18F-FDG in normal liver tissue (the mice without metastatic lesions) was 0.25 ± 0.02 and 0.22 ± 0.02, and the SUVmax and SUVmean values of 18F-FMISO in normal liver tissue was 0.17 ± 0.01 and 0.15 ± 0.007. Based on the SUVmax and SUVmean values of 18F-FDG, there was no significant difference between LoVo and HT29 tumor tissues (P = 0.683 and 0.339, respectively) (Table 1 and Fig. 2B). Moreover, both SUVmax and SUVmean values of 18F-FMISO in LoVo tumors were significantly greater than those of HT29 tumors (0.96 ± 0.189 vs. 0.67 ± 0.104 and 0.68 ± 0.139 vs. 0.41 ± 0.102, respectively; P = 0.001 and <0.00#, respectively) (Fig. 2C), suggesting that 18F-FMISO, but not 18F-FDG, may serve as an indicator of hepatic metastasis in CRC.

Figure 2
figure 2

(A) 18F-FDG/18F-FMISO-based micro-positron emission tomography (PET) images of liver metastases of LoVo and HT29 xenografts 7 weeks after injection with corresponding tumor cells. The gray outline area of the PET images of the mice with no liver metastasis represents the liver area. White arrows indicate the uptake of radiotracers in tumor tissues. (B) The timeline of micro-PET. (C) Quantification of micro-PET regions of interest analysis (ROI) of 18F-FDG and 18F-FMISO uptake in xenograft tumor tissues. (D) Demonstration of ROI delineation. *P < 0.05, n = 10 (LoVo) and n = 4 (HT29).

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Table 1 Comparison of 18F-FDG and 18F-FMISO SUV indices between LoVo and HT29 xenograft tumor tissues.
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LoVo cells have higher migratory and invasive abilities than HT29 cells in vitro

To reveal the molecular mechanism underlying the differences of metastatic potential and the abilities of radiotracer uptake between LoVo and HT29 cells in vivo, we performed wound healing and transwell assays to compare the migratory and invasive abilities of LoVo and HT29 cells in vitro25. As shown in Fig. 3A,C, the percentages of wounded healing area in LoVo cells at different time points were greater than those in HT29 cells (25.27 ± 0.6% vs. 20.46 ± 0.57% at 24 h and 67.3 ± 0.51% vs. 29.32 ± 0.43% at 48 h, respectively; P < 0.05). In addition, the number of migrating LoVo cells was significantly higher than that of HT29 cells (93.3 ± 5.13 vs. 27.6 ± 2.51, P < 0.05; Fig. 3B,D). These data suggest that LoVo cells are more prone to migration and invasion than HT29 cells in vitro.

Figure 3
figure 3

(A) LoVo and HT29 cell monolayers were scratched using pipette tips. The images were acquired at 0, 24, and 48 h after wound formation. Magnification 100×. (B) LoVo and HT29 cells were subjected to a Matrigel extracellular matrix cell invasion assay. The cells were allowed to invade for 72 h. The invading cells were stained with Giemsa and observed under a microscope at a magnification of 40×. (C) Quantification of cell wound closure (%) of LoVo and HT29 cells. (D) Quantification of cell invasion assay. *P < 0.05; n = 3.

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In vitro cellular radiotracer uptake analysis

To evaluate whether the abilities of radiotracer uptake in CRC cells were correlated with their metastatic potential, we performed time course analyses of cellular radiotracer uptake in LoVo and HT29 cells. As shown in Tables 2, 3 and Fig. 4, both 18F-FDG and 18F-FMISO were taken up into LoVo and HT29 cells in a time-dependent manner. At 30, 60, and 240 min, the uptake rates of both 18F-FDG (Fig. 4A) and 18F-FMISO (Fig. 4B) in LoVo cells were significantly higher than those in HT29 cells (for 18F-FDG, P = 0.003, 0.003, and 0.026, respectively; for 18F-FMISO, P = 0.049, <0.001, and 0.002, respectively). These results indicate that LoVo cells are more capable of taking up radiotracers than HT29 cells, suggesting that the ability of radiotracer uptake may be positively correlated with the metastatic potential of CRC cells.

Table 2 Comparison of in vitro uptake of 18F-FDG between LoVo and HT29 cells (%).
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Table 3 Comparison of in vitro uptake of 18F-FMISO between LoVo and HT29 cells (%).
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Figure 4
figure 4

Time courses of in vitro cellular uptake of 18F-FDG/18F-FMISO in LoVo and HT29 cells. Cells were incubated with 18F-FDG or 18F-FMISO for 30, 60, 120, and 240 min. Data are expressed as means ± standard deviation of the percentage of the injected dose (%ID) of 18F-FDG (A) or 18F-FMISO (B) per 5 × 105 cells. *P < 0.05; n = 3 (LoVo VS HT29).

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HIF-1α and GLUT-1 were induced more efficiently in LoVo cells than in HT29 cells

Since HIF-1α and GLUT-1 are closely associated with cancer metastasis, we next sought to determine and compare the expression of HIF-1α and GLUT-1 in LoVo and HT29 cells. As shown in Fig. 5, there was a stronger fluorescent staining of hypoxia-induced HIF-1α or serum starvation-induced GLUT-1 in LoVo cells than that in HT29 cells (71.06 ± 11.24 vs. 14.98 ± 5.74 and 29.3 ± 5.63 vs. 10.95 ± 4.47, P < 0.0001). In addition, the positive area percentage of GLUT-1 expression in LoVo and HT29 tumor tissues were 21.6% and 12.9%, respectively. The positive area percentage of HIF-1α expression in LoVo and HT29 tumor tissues were 11.4% and 9.1%, respectively. GLUT-1 and HIF-1α proteins were strongly stained in LoVo tumor tissues compared with HT29 tumor tissues (55.1 ± 2.85 vs. 32.94 ± 7.62 and 29.14 ± 2.63 vs. 23.13 ± 1.43, respectively, P < 0.05) measured by immunohistochemistry and expressed as mean density (Fig. 5D). Consistently, the results showed that the protein levels of both HIF-1α and GLUT-1 in LoVo tumor tissues were significantly higher than those in HT29 tissues (0.21 ± 0.006 vs. 0.16 ± 0.2 and 0.96 ± 0.03 vs. 0.69 ± 0.03, respectively, P < 0.05) (Fig. 5E–G). These results indicate that the expression of HIF-1α and GLUT-1 proteins in highly metastatic LoVo cells was induced more efficiently than that in HT29 cells both in vitro and in vivo.

Figure 5
figure 5

Comparison of induction of HIF-1α and GLUT-1 between LoVo and HT29 cells/tumor tissues. (A) Micrographs of immunofluorescence staining for nuclei (blue) and HIF-1α/GLUT-1 (green) in LoVo (upper panel) and HT29 (lower panel) cells (magnification, 200×). (B) and (C) Quantification of HIF-1α and GLUT-1 staining using Live cell Imaging System. (D) Immunohistochemical staining for GLUT-1/HIF-1α (brown) in LoVo (upper panel) and HT29 (lower panel) xenograft tumor tissues (magnification, 200×), respectively. (E) Western blot analyses of HIF-1α and GLUT-1 protein expression in LoVo (right lane) and HT29 (left lane) xenograft tumor tissues. (F) Quantification of immunohistochemical staining. (G) Quantification of Western blot analyses. ***P < 0.0001, **P < 0.001, *P < 0.05, n = 3.

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Correlation analysis

We next sought to determine the correlations between radiotracer uptake and HIF-1α/GLUT-1 protein expression. We measured the parameters of radiotracer uptake 1 h post 18F-FDG injection and 4 h post 18F-FMISO injection, which are the ideal time for radionuclide imaging. The results showed that in vitro cellular 18F-FDG uptake was significantly correlated with both GLUT-1 and HIF-1α expression (r = 0.929, P = 0.007 and r = 0.875, P = 0.022, respectively) (Fig. 6A,B), as well as in vitro (r = 0.945, P = 0.004 and r = 0.816, P = 0.045, respectively, Fig. 6C,D). For in vivo parameters, only 18F-FMISO SUV value had statistically significant differences in LoVo and HT29 liver metastasis tissue; therefore, we performed correlation analysis between 18F-FMISO SUVmax value and tumor markers. The result showed that the SUVmax value of 18F-FMISO was significantly correlated with GLUT-1 expression (r = 0.6357, P = 0.0145, Fig. 6E), but not with HIF-1α expression (r = 0.501, P = 0.068) (Fig. 6F).

Figure 6
figure 6

Correlation analyses between various parameters. (A) and (B) correlation of 18F-FDG uptake with GLUT-1 (A) and HIF-1α (B) expression in vitro. (C,D) correlation of 18F-FMISO uptake with GLUT-1 (C) and HIF-1α (D) expression in vitro. (E) and (F) correlation of in vivo values of 18F-FMISO SUVmax with GLUT-1 (E) and HIF-1α (F) expression in tumor tissues.

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Discussion

In the present study, we investigated the use of 18F-FDG/18F-FMISO-based PET imaging in CLM mouse models and demonstrated that LoVo cells have a stronger metastatic potential than HT29 cells. The underlying mechanisms were also examined. These data suggest 18F-FMISO-based PET imaging as a promising method in CLM monitoring.

18F-FMISO imaging has been used as a molecular probe in the assessment of hypoxic response in many types of xenograft tumor models including CRC26. Previous studies have shown that hypoxia duration is associated with increased risk of invasion and metastasis because of HIF-1α expression and a series of responses caused by HIF-1α expression under hypoxic conditions27,28. Therefore, hypoxic imaging can indicate the metastatic potential of cells.

Although Wang et al.29 have revealed the metastatic characteristics of SW620 and SW480 CRC cell lines using 18F-FDG and 18F-FLT, it remains unknown whether 18F-FDG and 18F-FMISO PET imaging may monitor cell glucose metabolism and hypoxic response and may be useful to predict liver metastatic potential. In this study, we used 18F-FDG and 18F-FMISO PET imaging to monitor the biological behavior and predict the CLM derived from LoVo and HT29 cells. The results demonstrated that the biological behavior of LoVo-derived tumors was significantly different from that of HT29-derived tumors, as evidenced by higher migration and invasion abilities in LoVo cells than in HT29 cells, as well as by shorter median survival of LoVo-CLM mice than that of HT29-CLM mice. These data are consistent with the results of 18F-FDG/18F-FMISO PET imaging showing that LoVo cells have stronger metastatic potential than HT29 cells. A study from Deng et al. also supports our findings30.

Tumor-specific markers are important in monitoring occurrence and development of tumors. Under hypoxic conditions, tumors exhibit enhanced glycolysis, angiogenesis invasion, and metastasis by inducing HIF-1α, which in turn promotes relevant gene expression31. Thus, detection of HIF-1α and GLUT-1 activity may accurately reflect metabolic ability of tumors or tumor cells. In this study, we examined HIF-1α and GLUT-1 expression and analyzed their correlation with radiotracer uptake. We observed a statistically significant correlation between 18F-FDG uptake and GLUT-1/HIF-1α expression, as well as between 18F-FMISO uptake in vitro. These data also support the correlation between GLUT-1/HIF-1α expression level and tumor metastatic potential.

Nevertheless, unlike the in vitro data, our study showed a weak correlation between 18F-FMISO SUVmax and GLUT-1 expression, but not HIF-1α. One possible reason is that the liver metastasis nodules were small in mice and the tumor hypoxic regions were also small. In the quantitative analysis of tumor hypoxia, the sensitivity of SUV measured by ROI is not as sensitive as that of bulk solid tumor. Another possible reason is the small number of CLM models. Kudo et al. showed that HIF-1α expression is heterogeneous in tumors32. In future experimental plans, we will further establish a CRC subcutaneous tumor mice model and increase the number of samples to further explore the correlation between FMISO SUV values and HIF-1 expression in CRC. In a previous study, Sato et al.33 claimed that the 18F-FMISO SUVmax in the primary site of oral squamous cell carcinoma was associated with HIF-1α expression and confirmed that 18F-FMISO uptake indicates the presence of hypoxic areas in tumor tissues. On the other hand, a study by Kawai et al.34 demonstrated that 18F-FMISO uptake does not correlate with HIF-1α expression in either newly diagnosed or recurrent malignant glioma patients. The relationship of 18F-FMISO uptake and HIF-1α (or GLUT-1) expression needs to be further confirmed. In the future, we plan to compare the differences in PET parameters between primary and metastatic lesions in a variety of animal models and CRC patients, and to study comprehensively the use of PET imaging in the detection and prediction of liver metastases from CRC.

Taken together, the uptake of 18F-FDG and 18F-FMISO can reflect the different biological behavior in LoVo and HT29 cells in vitro and in vivo. 18F-FMISO uptake may serve as a potential biomarker for detection of liver metastases in CRC, whereas its clinical utilization is warranted to validate