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基于局部微泡空化的抗血管生成疗法改善肝癌放疗治疗反应

Localized microbubble cavitation-based antivascular therapy for improving HCC treatment response to radiotherapy.

作者信息

Daecher Annemarie, Stanczak Maria, Liu Ji-Bin, Zhang Jie, Du Shisuo, Forsberg Flemming, Leeper Dennis B, Eisenbrey John R

机构信息

Department of Radiation Oncology, Thomas Jefferson University, Philadelphia, PA 19107, USA; Sidney Kimmel Medical College, Thomas Jefferson University, Philadelphia, PA 19107, USA.

Department of Radiation Oncology, Thomas Jefferson University, Philadelphia, PA 19107, USA.

出版信息

Cancer Lett. 2017 Dec 28;411:100-105. doi: 10.1016/j.canlet.2017.09.037. Epub 2017 Sep 29.

Abstract

Hepatocellular carcinoma (HCC) is the third leading cause of cancer mortality worldwide and the fastest growing malignancy in the United States. With a 5-year survival rate below 12%, effective therapies for HCC are needed. Current treatments for HCC include microwave and radiofrequency ablation, high intensity focused ultrasound, liver transplant, surgical resection, and localized embolizations. However, each of these approaches has some limitation, making it imperative to develop improved methods for sensitizing tumors prior to therapy. We hypothesized that the use of ultrasound-triggered microbubble destruction (UTMD), which sensitizes tumors to radiotherapy by inducing vascular endothelial cell apoptosis, will selectively sensitize malignant tissue to radiotherapy and improve outcomes. To test this, 18 nude rats were inoculated in the right liver lobe with Hu7.5 HCC cells and after tumor formation, received 5 Gy radiotherapy, UTMD, or UTMD prior to radiotherapy. Compared to radiotherapy alone, there was a 170% reduction in tumor growth 7 days post treatment and a 3.2X improvement in median survival time when radiotherapy was combined with UTMD. These results indicate that UTMD is an effective adjunct when combined with radiotherapy to treat HCC.

摘要

肝细胞癌(HCC)是全球癌症死亡的第三大主要原因,也是美国增长最快的恶性肿瘤。由于其5年生存率低于12%,因此需要有效的HCC治疗方法。目前HCC的治疗方法包括微波和射频消融、高强度聚焦超声、肝移植、手术切除和局部栓塞。然而,这些方法都有一定的局限性,因此必须开发改进的方法在治疗前使肿瘤敏感化。我们假设,通过诱导血管内皮细胞凋亡使肿瘤对放疗敏感的超声触发微泡破坏(UTMD)将选择性地使恶性组织对放疗敏感并改善治疗效果。为了验证这一点,18只裸鼠在右肝叶接种Hu7.5 HCC细胞,肿瘤形成后,接受5 Gy放疗、UTMD或放疗前的UTMD。与单纯放疗相比,治疗后7天肿瘤生长减少了170%,放疗联合UTMD时中位生存时间提高了3.2倍。这些结果表明,UTMD与放疗联合治疗HCC时是一种有效的辅助手段。

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