Prophylaxis against carcinogenesis in three kinds of unestablished tumor models via IL12-gene-engineered MSCs

被引:59
作者
Chen, Xian-cheng
Wang, Rui
Zhao, Xia
Wei, Yu-quan
Hu, Min
Wang, Yang-sheng
Zhang, Xiao-wei
Zhang, Ru
Zhang, Lin
Yao, Bin
Wang, Lian
Jia, Yong-qian
Zeng, Ting-ting
Yang, Jin-liang
Kan, Bing
Lin, Xiao-juan
Lei, Song
Deng, Hong-xin
Wen, Yan-jun
Mao, Yong-qiu
Li, Jiong
机构
[1] Sichuan Univ, W China Med Sch, Natl Key Lab Biotherapy, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, W China Med Sch, Ctr Canc, Chengdu 610041, Sichuan, Peoples R China
[3] Sichuan Univ, W China Hosp 2, Dept Gynecol & Obstet, Chengdu 610041, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
D O I
10.1093/carcin/bgl069
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Mesenchymal stem cells (MSCs) were adenovirally engineered to secrete interleukin-12 (AdIL-12-MSCs) and evaluated for their anticarcinogenesis efficacy against three kinds of unestablished tumor models including B16 melanoma, LLC Lewis lung cancer and HCC hepatoma. Injection of AdIL-12-MSCs into protected mice before tumor inoculation prevented all of 12 mice in B16 preventive groups, 10 out of 12 in LLC lung cancer model and 11 out of 12 mice in HCC hepatoma model from developing tumors, whereas the control groups pre-receiving PBS were validated for 100% carcinogenesis; the tumor formation rates in free-AdIL-12 and vacant MSC groups were unveiled between similar to 83 and 100% even with plentiful angiogenesis and newborn lymphatic vessels, as well as distant metastases. As a novel approach, AdIL-12-MSC has revealed expected preventive effects on carcinogenesis (P < 0.01) with low-toxic, broad-spectrum and long-range superiorities. In conclusion, our data indicate that AdIL-12-MSC possess the potential for tropism to preclinical tumor lesions and deprives surviving or hibernating tumor cells, which have escaped from conventional treatments, of revival and recurrence.
引用
收藏
页码:2434 / 2441
页数:8
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