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首页> 外文期刊>British Journal of Cancer >Vascular disrupting action of electroporation and electrochemotherapy with bleomycin in murine sarcoma
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Vascular disrupting action of electroporation and electrochemotherapy with bleomycin in murine sarcoma

机译:博来霉素对小鼠肉瘤的电穿孔和电化学疗法的血管破坏作用

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Electrochemotherapy has a direct cytotoxic effect on tumour cells, and presumably, a vascular disrupting effect. In this study, on the basis of the prediction of the mathematical model, histological evaluation and physiological measurements of the tumours were carried out to confirm that electroporation and electrochemotherapy of tumours have a vascular disrupting action. In the study, SA-1 solid subcutaneous sarcoma tumours in A/J mice were treated by bleomycin (BLM) given intravenously (1?mg?kg?1), application of electric pulses (8 pulses, 1040?V, 100?μs, 1?Hz) or a combination of both – electrochemotherapy. The vascular effect was determined by laser Doppler flowmetry, power Doppler ultrasonographic imaging and Patent blue staining. The extent of tumour hypoxia was determined immunohistochemically by hypoxia marker pimonidazole and partial pressure of oxygen (pO2) in tumours by electron paramagnetic resonance oximetry. Electrochemotherapy with BLM induced good antitumour effect with 22 days, tumour growth delay and 38% tumour cures. The application of electric pulses to the tumours induced instant but transient tumour blood flow reduction (for 70%) that was recovered in 24?h. During this tumour blood flow reduction, we determined an increase in hypoxic tumour area for up to 30%, which was also reflected in reduced tumour oxygenation (for 70%). According to the described mathematical model, endothelial cells lining in tumour blood vessels are exposed to a ~40% higher electric field than the surrounding tumour cells, and therefore easily electroporated, allowing access of high BLM concentration to the cytosol. Consequently, electrochemotherapy has, besides the immediate vascular disrupting action, also a delayed one (after 24?h), as a consequence of endothelial cell swelling and apoptosis demonstrated by extensive tumour necrosis, tumour hypoxia, prolonged reduction of tumour blood flow and significant tumour growth delay, and tumour cures. Our results demonstrate that in addition to the well-established direct cytotoxic effect on tumour cells, electrochemotherapy also has an indirect vascular disrupting action resulting altogether in extensive tumour cell necrosis leading to complete regression of tumours.
机译:电化学疗法对肿瘤细胞有直接的细胞毒性作用,大概是血管破坏作用。在这项研究中,在数学模型的预测基础上,对肿瘤进行了组织学评估和生理测量,以确认肿瘤的电穿孔和电化学疗法具有血管破坏作用。在这项研究中,通过静脉注射博莱霉素(BLM)(1?mg?kg?1),施加电脉冲(8个脉冲,1040?V,100?μs)来治疗A / J小鼠的SA-1实体皮下肉瘤,1?Hz)或两者结合-电化学疗法。通过激光多普勒血流仪,功率多普勒超声成像和专利蓝染色确定血管作用。肿瘤缺氧的程度通过缺氧标记物pimonidazole进行免疫组织化学测定,并通过电子顺磁共振血氧测定法测定肿瘤中的氧分压(pO2)。 BLM电化学疗法具有良好的抗肿瘤作用,有效期22天,肿瘤生长延迟,治愈率达38%。在肿瘤上施加电脉冲可导致瞬时但短暂的肿瘤血流减少(70%),可在24小时内恢复。在这种减少肿瘤血流量的过程中,我们确定缺氧肿瘤面积最多增加30%,这也反映在减少的肿瘤氧合(70%)上。根据所描述的数学模型,肿瘤血管内衬的内皮细胞暴露于比周围肿瘤细胞高约40%的电场,因此易于电穿孔,从而允许高BLM浓度进入细胞质。因此,由于广泛的肿瘤坏死,肿瘤缺氧,延长的肿瘤血流减少和显着的肿瘤表现出内皮细胞肿胀和凋亡,因此电化学疗法除了具有立即的血管破坏作用外,还具有延迟的作用(24小时后)。生长延迟和肿瘤治愈。我们的结果表明,除了对肿瘤细胞已确立的直接细胞毒性作用外,电化学疗法还具有间接的血管破坏作用,导致广泛的肿瘤细胞坏死,从而导致肿瘤完全消退。

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