The effects of a picosecond pulsed electric field on angiogenesis in the cervical cancer xenograft models

血管生成 医学 川地31 血管内皮生长因子 病理 免疫印迹 赫拉 免疫组织化学 宫颈癌 新生血管 微血管 癌细胞 癌症研究 癌症 化学 细胞 内科学 血管内皮生长因子受体 基因 生物化学
作者
Limei Wu,Chenguo Yao,Zhengai Xiong,Ruizhe Zhang,Zhiliang Wang,Yutong Wu,Qin Qin,Yuanyuan Hua
出处
期刊:Gynecologic Oncology [Elsevier]
卷期号:141 (1): 175-181 被引量:13
标识
DOI:10.1016/j.ygyno.2016.02.001
摘要

The application of picosecond pulsed electric field (psPEF) is a new biomedical engineering technique used in cancer therapy. However, its effects on cervical cancer angiogenesis are not clear. Therefore, the aim of the present study is to investigate the effects of psPEF on angiogenesis in cervical cancer xenograft models.Xenograft tumors were created by subcutaneously inoculating nude mice (athymic BALB/c nu/nu mice) with HeLa cells, then were placed closely between tweezer-type plate electrodes and subjected to psPEF with a gradually increased electric field intensity (0kV/cm, 50kV/cm, 60kV/cm, 70kV/cm). The direct effect on tumor tissue was observed by hematoxylin and eosin (H&E) staining and transmission electron microscopy (TEM). The changes of blood vessels and oxygen saturation (sO2) of tumors were monitored in vivo by photoacoustic tomography (PAT). The microvessel density (MVD), vascular endothelial growth factor (VEGF) and hypoxia-inducible transcription factors (HIF-1α and HIF-2α) were detected by immunohistochemical technique (IHC). Their protein expressions and gene transcription levels were evaluated using western blot (WB) and quantitative reverse transcription and polymerase chain reaction (RT-PCR).PsPEF induced obvious necrosis of cervical cancer tissue; with the increasing of electric field intensity, the MVD, vascular PA signal and sO2 values declined significantly. The protein expression and gene transcription levels of VEGF, HIF1α and HIF2α were significantly decreased at the same time.PsPEF exhibited dramatic anti-tumor and anti-angiogenesis effects in cervical cancer xenograft models by exerting direct effect on cancer cells and vascular endothelial cells and indirect effect on tumor angiogenesis-related factors.

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