Liang XM, Tang GY, Cheng YS, Zhou B. Evaluation of a rabbit rectal VX2 carcinoma model using computed tomography and magnetic resonance imaging. World J Gastroenterol 2009; 15(17): 2139-2144
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Dr. Ying-Sheng Cheng, Professor, Department of Radiology, the Tenth People’s Hospital of Shanghai Tongji University, No. 301, Yanchang Middle Road, Shanghai 200072, China. firstname.lastname@example.org
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World J Gastroenterol. May 7, 2009; 15(17): 2139-2144 Published online May 7, 2009. doi: 10.3748/wjg.15.2139
Evaluation of a rabbit rectal VX2 carcinoma model using computed tomography and magnetic resonance imaging
Xin-Mei Liang, Guang-Yu Tang, Ying-Sheng Cheng, Bi Zhou
Xin-Mei Liang, Bi Zhou, Department of Radiology, the Sixth People’s Hospital of Shanghai Jiaotong University; Institute of Medical Imaging of Shanghai Jiaotong University, No. 600, Yishan Road, Shanghai 200233, China
Guang-Yu Tang, Ying-Sheng Cheng, Department of Radiology, the Tenth People’s Hospital of Shanghai Tongji University, No. 301, Yanchang Middle Road, Shanghai 200072, China
ORCID number: $[AuthorORCIDs]
Author contributions: Liang XM and Cheng YS contributed equally to this work; Liang XM and Cheng YS designed the research; Liang XM and Zhou B performed the research; Liang XM analyzed the data and wrote the paper; Tang GY and Cheng YS revised the paper.
Correspondence to: Dr. Ying-Sheng Cheng, Professor, Department of Radiology, the Tenth People’s Hospital of Shanghai Tongji University, No. 301, Yanchang Middle Road, Shanghai 200072, China. email@example.com
Received: February 6, 2009 Revised: March 8, 2009 Accepted: March 15, 2009 Published online: May 7, 2009
AIM: To establish a rabbit rectal VX2 carcinoma model for the study of rectal carcinoma.
METHODS: A suspension of VX2 cells was injected into the rectum wall under the guidance of X-ray fluoroscopy. Computed tomography (CT) and magnetic resonance imaging (MRI) were used to observe tumor growth and metastasis at different phases. Pathological changes and spontaneous survival time of the rabbits were recorded.
RESULTS: Two weeks after VX2 cell implantation, the tumor diameter ranged 4.1-5.8 mm and the success implantation rate was 81.8%. CT scanning showed low-density foci of the tumor in the rectum wall, while enhanced CT scanning demonstrated asymmetrical intensification in tumor foci. MRI scanning showed a low signal of the tumor on T1-weighted imaging and a high signal of the tumor on T2-weighted imaging. Both types of signals were intensified with enhanced MRI. Metastases to the liver and lung could be observed 6 wk after VX2 cell implantation, and a large area of necrosis appeared in the primary tumor. The spontaneous survival time of rabbits with cachexia and multiple organ failure was about 7 wk after VX2 cell implantation.
CONCLUSION: The rabbit rectal VX2 carcinoma model we established has a high stability, and can be used in the study of rectal carcinoma.
Rectal carcinoma is a common malignant tumor of the gastrointestinal tract. Imaging examination plays an important role in its identification, diagnosis, preoperative staging, treatment decision, and postoperative assessment[1–3]. Currently, experimental animal models of rectal carcinoma are often induced by chemical carcinogens[4–6]. This kind of methods requires lots of time and individual variations can be very large. In this study, a rabbit rectal carcinoma model was established and evaluated, which can be monitored dynamically by computed tomography (CT) and magnetic resonance imaging (MRI) and used in diagnosing and staging rectal carcinoma.
MATERIALS AND METHODS
Twenty-two (4-5 mo old) New Zealand white rabbits, weighing 2.4-2.9 kg, were used in this study, and the breeding rabbits were donated by Professor Bin Hu, Department of Ultrasound, Sixth People’s Hospital of Shanghai Jiaotong University, China.
Preparation for surgery
Experimental rabbits were lavaged 24 h prior to surgery. Mannitol (20%) was prepared with warm water at a ratio of 1:1 and the lavage dose was approximately 250 mL per rabbit. Lavaged rabbits were fasted with free access to water prior to surgery. VX2 tumor cells were grown in the hind leg muscle of rabbits and harvested for the preparation of suspended tumor cells at a concentration of 1-2 × 107/mL.
Establishment of rectal carcinoma model
Experimental rabbits were anesthetized with 30 mg/kg pentobarbital sodium via the ear vein. Rabbits were placed at a dorsal position with their legs fixed. A 7-cm long sterilized plastic hollow pipe, 7 mm in diameter, was inserted into the anus to brace the rectal cavity. A 22G transfixion pin was injected into approximately 4-5 cm of the rectal wall around the anus. A contrast medium (0.2 mL, Ultravist 300) was injected with its distribution monitored by X-ray fluoroscopy. If its border was ill-defined and dispersed, the needle point would be in a gap region between the outside of the organ and the rectal wall. Then, the puncture needle was reinserted into the rectal wall until the border of contrast medium became sharply margined. At this point, 0.2 mL of suspended VX2 cells was injected, then 0.1-0.2 mL of normal sodium was injected to fully rinse all the VX2 cells into the rectal wall. After 5 min, the needle was withdrawn slowly. The rabbits were allowed to have normal food following recovery from anesthesia.
CT and MRI scanning of tissue sections
Rabbits were anesthetized with 30 mg/kg pentobarbital sodium before CT and MRI scanning of tissue sections at 2-, 3-, 4-, 5- and 6-wk intervals after VX2 cell implantation. CT scanning was performed using a GE LIGHT SPEED VCT 64 CT set with the following parameters: 80 kV, 100 mA, 14-16 cm in field of view (FOV), 512*512 matrix, 1.25 mm section thickness, and 1.25 mm section interval. A contrast medium (Ultravist 300) was injected at 0.5 mL/s and 1.5-2.0 mL/kg. Arterial phase scanning was started 15 s after contrast medium injection and after 30 s during the portal venous phase. The image was processed at the ADW4.0 workstation. MRI scanning was performed by a Philips Achieva 3.0 imager, with the rabbit placed at a supine position in a phased-array articular genu coil. MRI sequences included the pre-contrast T1W-TSE, gadolinium-enhanced T1W-TSE, and T2W-TSE sequences in the axial plane (TR-2727 ms, TE-100 ms, 2.0 mm section thickness 2.0 mm, and section interval 0.8 mm), T2_TSE_SPAIR sequence in the axial plane (TR-4341 ms, TE-62 ms, section thickness 2.0 mm, and section interval 0.2 mm), and PD_SPAIR sequence in the coronal planes (TR-4710 ms, TE-30 ms, section thickness 2.0 mm, and 0.2 mm section interval 0.2 mm). The contrast medium (Magnevist) was injected at 0.5 mL/s and 1.5-2.0 mL/kg. Enhancement scanning was started 20 s after contrast medium injection, and the image was processed at a View Forum R5.1 V1L1 workstation.
Measurement of tumor volume
Gross tumor volume (V) was measured following the equation: V = 0.5 (a × b2), where a represents the maximum tumor diameter, and b represents the minimum tumor diameter. Tumor growth rate (TGR) was calculated following the equation: TGR = (V2 - V1)/V1× 100%, where V1 represents the gross tumor volume measured at an earlier time point and V2 represents the gross tumor volume measured at a later time point.
Histopathological changes in rabbit rectal VX2 carcinoma model
Three rabbits were sacrificed after each CT and MRI scanning at 2-6 wk intervals after VX2 cell implantation for observation of pathological changes in the rectal VX2 carcinoma model. Autopsies were also performed after spontaneous death of the rabbits. Tumor location, size, activity, circumscription, and metastasis were observed grossly. The rectum-implanted tumor and the major organs involved were fixed in formalin and embedded in paraffin. Tumor tissue was cut into sections, which were stained with hematoxylin-eosin (H&E), and evaluated under a light microscope.
Data were presented as mean ± SD. Gross tumor volumes at an earlier and later time point were compared by Student’s t test. Statistical analyses were performed using SPSS 11.0 software. P < 0.05 was considered statistically significant.
Twenty-two New Zealand white rabbits were used to establish the model. Eighteen of them developed primary tumors with a success rate of 81.8%.
Tumor implanted in the rectal wall of each rabbit could be detected by CT scanning 2 wk after VX2 cell implantation. The appearance of rectal enteric cavity at this time point was still normal without obvious stricture. However, part of the rectal wall exhibited irregularly intensified armillary after enhancement (Figure 1A). The gross tumor volume was increased 3 wk after VX2 cell implantation, and appeared as a small lump with low density or isodensity on CT images. The boundary between the tumor and normal rectal wall could not be clearly distinguished. However, the rectal enteric cavity became elliptical with stricture, allowing the tumor margin to be distinguished from its surrounding tissue (Figure 1B). After 4 wk, the gross tumor volume was increased, the rectal wall was thickened, and the rectal enteric cavity became flatter, with increased stricture. Necrosis could be detected in the middle of the tumor, and the surrounding tissue was involved at different degrees. CT scanning showed that the tumor appeared to have an intensified, solid marginal zone and a central region with low density but without intensification. In contrast, the surrounding tissue was intensified as the tumor (Figure 1C). CT scanning revealed significant stricture of the tumor, which was fixed to the pelvic wall and rectal enteric cavity 5 wk after VX2 cell implantation (Figure 1D). After 6 wk, the rectal enteric cavity was almost compressed to the point of closure and metastatic nodes were detected in the lung (Figure 1E) and liver (Figure 1F), as in the seroperitoneum. The metastatic nodes appeared in the lung earlier and much more obviously than in the liver, since the blood supply in the lower part of rectum returns to the inferior vena cava but not to the hepatic portal vein.
Figure 1 CT enhancement scanning images of rectal wall 2(A), 3(B), 4(C), and 5(D) wk after VX2 cell implantation in the experimental rabbits, and images of metastatic nodes detected in the lung (E) and liver (F), respectively.
MRI showed that the signal of VX2 tumor was low on T1-weighted imaging (T1WI), resulting in the detection of an indistinct boundary, and high on T2-weighted imaging (T2WI), allowing clear visualization of the boundary. In addition, the signal of VX2 tumor in PD sequence was higher than that on T1WI. Tumor boundary could be distinguished from its surrounding tissue after enhancement. Necrosis with low signals, but without intensification after enhancement, could be detected in the middle of the primary tumor 4 wk after VX2 cell implantation. MRI and CT demonstrated similar growth and metastasis of the tumor. However, MRI identified more precisely the tumor boundary, size and infiltration, and infection foci than CT scanning. MRI of the tumor at 2-, 3-, 4-, and 5-wk intervals after VX2 cell implantation are shown in Figure 2. The gross tumor volume (V) and the TGR at these time points were also calculated (Table 1). The TGR at each time point was quite different (P < 0.0001), but the fastest growth of tumor was observed 3 wk after VX2 cell implantation.
Table 1 Gross tumor volume and TGR after tumor implantation.
Time after implantation
5.029 ± 0.544
4.129 ± 0.475
46.180 ± 14.583
16.783 ± 1.387
9.942 ± 1.326
848.239 ± 270.715
19.419 ± 1.150
15.800 ± 1.255
2443.569 ± 480.966
24.763 ± 1.762
22.163 ± 1.388
6163.157 ± 1181.274
Tumor volume (V) = 0.5 (a × b2), where a and b represent the maximum and minimum tumor diameters, respectively; TGR = (V2 - V1)/V1× 100%, where V1 represents the gross tumor volume measured at an earlier time point and V2 represents the gross tumor volume measured at a later time point.
Figure 2 MRI of T2-TSE-SPAIR 2(A), 3(B), 4(C), and 5(D) wk after VX2 cell implantation in the experimental rabbits.
Macroscopic image of the resected tumor appeared as a single node with an obscure boundary and affluent vascellum (Figure 3A and B). Metastasis outside the rectal wall was not detected until 4 wk after VX2 cell implantation. The rectal wall was thickened due to different degrees of enteric cavity stricture. No enterectasis or rectum obstruction was observed. Necrosis appeared in the middle of the tumor 4 wk after VX2 cell implantation, with enteric cavity stricture and enterectasis, as well as metastasis outside the rectal wall in the pelvic cavity. Metastases to the lung and liver, and seroperitoneum and rectum obstruction were detected 6 wk after VX2 cell implantation. However, the metastasis in the liver was not as obvious as that in the lung, and sometimes it was not detectable, because the metastasis in the liver was not sufficiently large to be visualized. The experimental rabbits developed cachexia and multiple organ failure, and died spontaneously about 7 wk after VX2 cell implantation.
Figure 3 Characteristics of isolated rectal carcinoma specimens (A, B) and light microscope images of HE stained tissue sections (C, × 40; D, × 100).
Tumor tissue sections were stained with H&E and evaluated under a light microscope. Infiltrating tumor cells were visible and the interstitial tissue boundary was not distinct. Minimal connective tissue was observed, and dispersed tumor cells were found with separation of fibers. Fresh capillaries were abundant (Figure 3C), consistent with the large, irregular tumor volume. Cytoplasm of the tumor cells was abundant, and pale red in color. There was an abnormal number of mitotic nuclei. Hypertrophic nuclei were also found, varying in shape, size, and color (Figure 3D). Two weeks after VX2 cell implantation, the tumor grew in the rectal wall with no involvement of its peripheral tissue. However, by 3 wk after VX2 cell implantation, the tumor grew through the rectal wall with the mesorectal fascia tissue involved 4 wk after VX2 cell implantation.
Since lymph in the gastrointestinal tract is very rich, the survival rate of heterogeneic tumor tissue transplanted to the intestine wall of experimental animals is practically zero. Because of this, smaller animal models are often used in the study of rectal carcinoma. Experimental animal models can be established by repeated injection of chemical carcinogens into the abdominal cavity of animals, or repeated lavaging of the intestinal tract. However, these methods are time consuming and their success rate is low. Furthermore, these small animal models cannot contribute to the diagnosis of rectal carcinoma.
VX2 cells can be implanted into rabbits where they can grow. It has been shown that this cell line, implanted into the muscle, kidney, liver, lung, pleura, ossature, and mammary gland of rabbits, can produce an in situ tumor model that mimics the human condition[7–12]. The implantation techniques for VX2 cells include implanting a small lump of VX2 tumor tissue and injecting a suspension of VX2 cells directly or under the guidance of B-mode ultrasound or CT. Wang et al demonstrated that laparotomy could be used to establish a rabbit model of rectal VX2 carcinoma, with a success rate of 60%. Considering the substantial damage caused by laparotomy, we established the rabbit model of rectal VX2 carcinoma by injecting a suspension of VX2 cells into the rectal wall through the skin of the anorectum under the guidance of X-ray fluoroscopy. CT or MRI showed the implanted tumor in the rectal wall 2 wk after VX2 cell implantation. The involved tissue around the rectum was observed and metastases to the lung and liver were detectable 4 and 6 wk, respectively, after VX2 cell implantation. The success rate of this method was 81.8%.
This rabbit rectal VX2 carcinoma model was evaluated by CT scanning, MRI, and histopathology.
CT has many advantages in monitoring rectal tumor by displaying its location, size, shape, peripheral tissue and lymph node involvement. Recently, with the update of CT instruments and CT imaging techniques, the sensitivity and specificity of CT in detection of tumors have been greatly improved. Multi-section CT (MSCT) is more advantageous than ordinary CT, by reducing the shadow of motion and displaying dynamic enhancement effects[16–18]. Furthermore, CT plays an important role in preoperative staging of rectal carcinoma, especially in detecting metastasis in the lung and liver. CT scanning has been recommended to patients with colorectal cancer[20–22]. In this study, MSCT showed the growth of tumor and its surrounding tissue, as well as distant organ metastasis, suggesting that CT scanning is an ideal method for monitoring VX2 rectal carcinoma.
Since the location of the rectum is relatively fixed, tumor tissue can be observed by contrast with the peripheral fat, and is seldom affected by the shadows that result from respiration. MRI is a good imaging technique for detection of rectal tumor and can show the layers of the rectal wall, including the mucosa with a low-intensity signal, submucosa with a high-intensity signal, muscularis propria with a weak-intensity signal, perirectal fat with a high-intensity signal, and mesorectal fascia with a low-intensity signal. T1WI can be used to evaluate fatty infiltration around the rectum, while T2WI can display the infiltration depth in the rectal wall and the relation between inherent muscle layers and mesorectal fascia. The most significant advantage of MRI in rectal carcinoma staging is its ability to describe the correlation between tumor and mesorectal fascia[23–25]. MRI can determine the circumferential resection margin (CRM). Induction of 3.0T magnetic resonance and improvement in phased-array coils make MRI display the CRM much more precisely. Its accuracy for the prediction of CRM is consistent with histopathological assessment of specimens after surgery[29–32]. It has also been reported that MRI can predict the infiltration depth of rectal tumor in the range of 0.5 mm, which is consistent with histopathology results. MRI is more sensitive in detecting early stage tumor growth than CT, especially in measuring the tumor size. In addition, MRI can display metastasis of tumor to lymph nodes.
This animal model is easy to establish, reproducible, and induces minimal damage to experimental animals. In addition, the tumor growth time is short. The growth and metastasis of rectal VX2 carcinoma in rabbits are similar to those in humans. Therefore, it can be used in the study of rectal carcinoma.
Currently, experimental animal models of rectal carcinoma are often induced by chemical carcinogens, which is time consuming. It has been shown that implantation of VX2 cells into the muscle, kidney, liver, lung, pleural, ossature, and mammary gland of rabbits can produce an in situ tumor model that mimics the human condition.
The implantation techniques for VX2 cells include implanting a small lump of VX2 tumor tissue and injecting a suspension of VX2 cells directly, or under the guidance of B-mode ultrasound and computed tomography.
Innovations and breakthroughs
It is feasible to establish a rabbit rectal VX2 carcinoma model by injecting a suspension of VX2 cells into the rectum wall under the guidance of X-ray fluoroscopy. This model is similar to human rectal carcinoma models in terms of tumor pathology, development, and metastasis.
This rabbit rectal VX2 carcinoma model can be used in examination, staging and diagnosis of rectal carcinoma.
VX2 cell strain, a squamous carcinoma strain induced by Shope virus, can be implanted in rabbits.
The animal model presents many analogies to human rectal carcinoma in terms of pathological findings and tumor development.
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