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Updated: Jun 30, 2026

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Development and Angiographic Use of the Rabbit VX2 Model for Liver Cancer
Published on: January 7, 2019
Gene expression and MR diffusion-weighted imaging after chemoembolization in rabbit liver VX-2 tumor model
You-Hong Yuan1, En-Hua Xiao, Jian-Bin Liu
1Department of Radiology, Hunan Province People's Hospital, Changsha, Hunan Province, China. heyuanyouhong@yahoo.com.cn
World Journal of Gastroenterology
|September 24, 2008
Summary
Chemoembolization temporarily increases VX-2 liver tumor proliferation while decreasing infiltration potential. Apparent diffusion coefficient (ADC) on MRI diffusion-weighted imaging (DWI) may indirectly reflect this tumor cell proliferation.
Area of Science:
- Oncology
- Radiology
- Biochemistry
Background:
- VX-2 liver tumors in rabbits are a model for human hepatocellular carcinoma.
- Chemoembolization is a standard treatment for liver tumors.
- Understanding dynamic changes in tumor markers and imaging is crucial for treatment assessment.
Purpose of the Study:
- To investigate dynamic changes in PCNA, Bax, nm23, and E-cadherin expression post-chemoembolization.
- To correlate these marker expressions with apparent diffusion coefficient (ADC) values from MR diffusion-weighted imaging (DWI).
- To assess the utility of DWI in reflecting tumor characteristics after treatment.
Main Methods:
- Forty New Zealand rabbit VX-2 liver tumor models were used.
- Diffusion-weighted imaging (DWI) was performed periodically after chemoembolization.
- Histopathology and SABC immunohistochemistry were used to evaluate protein expression.
Main Results:
- PCNA expression was higher in VX-2 tumors than normal tissue; nm23, Bax, and E-cadherin were lower.
- PCNA and nm23 expression peaked in the tumor periphery post-treatment.
- A linear correlation was found between PCNA expression and ADC in the tumor periphery.
Conclusions:
- Chemoembolization temporarily increases VX-2 tumor cell proliferation while reducing infiltration and metastasis potential.
- ADC values obtained via DWI can indirectly indicate tumor cell proliferation dynamics after chemoembolization.

