Department of Ultrasound, Shanghai Jiaotong University Affiliated First People's Hospital, Shanghai, China.
J Gene Med. 2014 Jan-Feb;16(1-2):28-39. doi: 10.1002/jgm.2755.
Recombinant adeno-associated virus (rAAV) is recognized as a promising vector for cancer gene therapy, although its low transfer efficiency in less permissive cells limits extensive application. Our previous studies reported that ultrasound-targeted microbubble (MB) destruction (UTMD) enhanced rAAV transfer in its permissive retinal cells. In the present study, we investigated whether UTMD increased rAAV transfer in less permissive human renal cell carcinoma (hRCC) cells and tumors.
hRCC cells were treated with rAAV2 under different conditions of UTMD, and the viral transfer efficiency and cell viability were analyzed. Fifty-two male nude mice (BALB/c) implanted with hRCC cells were randomly assigned to four groups consisting of rAAV, rAAV + ultrasound and rAAV + UTMD (20 µl and 40 µl of MBs). UTMD was initiated immediately after intratumoral viral injection, and viral transfer efficiency and tumor volumes were analyzed at 12 weeks after infection.
The efficiency of non-augmented transfer of rAAV2 into hRCC cells was low (17.28 ± 2.44%). The use of UTMD enhanced viral transfer efficiency by two- to three-fold, and enhanced viral genomic DNA by more than nine-fold, without decreasing cell viability. In vivo studies also showed that UTMD increased rAAV2 transfer in tumor. The enhancements were maintained for a period of 12 weeks. Tumor growth in mice was inhibited by UTMD treatment, and UTMD treatment augmented by MBs (40 µl) produced an even stronger effect.
UTMD enhanced rAAV2 transfer into less permissive RCC cells and tumors, resulting in inhibition of tumor growth, which suggests that UTMD may be a useful delivery tool for cancer gene therapy.
重组腺相关病毒(rAAV)被认为是一种很有前途的癌症基因治疗载体,尽管其在不允许的细胞中的转导效率较低,限制了其广泛应用。我们之前的研究报告称,超声靶向微泡(MB)破坏(UTMD)增强了其允许的视网膜细胞中的 rAAV 转移。在本研究中,我们研究了 UTMD 是否增加了不允许的人肾细胞癌(hRCC)细胞和肿瘤中的 rAAV 转移。
hRCC 细胞在不同的 UTMD 条件下用 rAAV2 处理,并分析病毒转导效率和细胞活力。52 只雄性裸鼠(BALB/c)植入 hRCC 细胞后,随机分为 rAAV、rAAV+超声和 rAAV+UTMD(20μl 和 40μl 的 MB)四组。在肿瘤内病毒注射后立即启动 UTMD,感染 12 周后分析病毒转导效率和肿瘤体积。
rAAV2 非增强转导进入 hRCC 细胞的效率较低(17.28±2.44%)。UTMD 增强了病毒转导效率,提高了两倍到三倍,提高了病毒基因组 DNA 的含量超过九倍,而不降低细胞活力。体内研究也表明,UTMD 增加了肿瘤内 rAAV2 的转移。这种增强作用可以维持 12 周。UTMD 治疗抑制了肿瘤生长,而 40μl MB 的 UTMD 增强了治疗效果。
UTMD 增强了不允许的 RCC 细胞和肿瘤中 rAAV2 的转移,导致肿瘤生长抑制,这表明 UTMD 可能是癌症基因治疗的一种有用的传递工具。