|
|
Targeted IL-24 gene therapy inhibits cancer recurrence after liver tumor resection by inducing tumor cell apoptosis in nude mice |
Yong-Jiu Yang, Da-Zhi Chen, Li-Xin Li, Qin-Song Sheng, Zhong-Kui Jin and De-Fang Zhao |
Beijing, China
Author Affiliations: Department of Hepatobiliary Surgery, Beijing Chaoyang Hospital, Capital Medical University, Beijing 100020, China (Yang YJ, Chen DZ, Li LX, Sheng QS, Jin ZK and Zhao DF); Department of General Surgery, Beijing Chuiyangliu Hospital (Beijing Minimally Invasive Hospital), Beijing 100022, China (Yang YJ)
Corresponding Author: Da-Zhi Chen, MD, Department of Hepatobiliary Surgery, Beijing Chaoyang Hospital, Capital Medical University, Beijing 100020, China (Tel: 86-10-85231503; Email: chendazhi@medmail.com.cn) |
|
|
Abstract BACKGROUND: Interleukin-24 (IL-24) is a novel candidate tumor suppressor that induces tumor cell apoptosis experimentally in a variety of human malignant cells including liver cancer cells. The present study was conducted to investigate the potential effect of recombinant adeno-associated virus (rAAV)-mediated IL-24 gene therapy on tumor recurrence and metastasis by inducing tumor cell apoptosis in a hepatocellular carcinoma (HCC) model in nude mice.
METHODS: We established a recurrent and metastatic HCC model in nude mice and constructed a rAAV vector carrying alpha-fetoprotein (AFP) promoter for expressing the IL-24 gene (rAVV/AFP/IL-24). The vector was administered by regional injection (liver incisal margin). AFP was detected by radiation immunoassay. Histological evaluation of tumor recurrence and metastasis was performed for the liver and lung. The effect of tumor cell apoptosis was confirmed by TUNEL analysis.
RESULTS: IL-24 gene therapy prevented tumor recurrence and metastasis, as evidenced by marked decreases in the number of metastatic tumor nodules and tumor volume in the liver and lung. At the same time, serum AFP concentration decreased markedly in the IL-24 group compared with the control or rAAV groups (P<0.05). IL-24 gene therapy inhibited tumor recurrence and metastasis as evidenced by the induction of tumor cell apoptosis.
CONCLUSION: The results demonstrated that targeted IL-24 gene therapy was effective in the prevention of postoperative recurrence and metastasis in an HCC nude mice model by induction of tumor cells apoptosis with potential minimum tumor burden.
|
|
|
|
|
Cite this article: |
Yang YJ,
Chen DZ,
Li LX,
et al.
Targeted IL-24 gene therapy inhibits cancer recurrence after liver tumor resection by inducing tumor cell apoptosis in nude mice.
Hepatobiliary Pancreat Dis Int
2009;
8(2):
174-178. DOI:
|
|
|
|
URL: |
http://dx.doi.org/ OR http://www.hbpdint.com/EN/Y2009/V8/I2/174 |
|
|
|