Kurisetty Vittal, Bryan Brad A
Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, El Paso, Texas, USA.
Angiol Open Access. 2013 Apr 8;1. doi: 10.4172/2329-9495.1000102.
Angiosarcomas are very aggressive, rare malignant tumors that originate from vascular or lymphatic vessels and primarily occur following chemical exposure or radiation therapy. Tumor response to either chemotherapy, radiation, or novel anti-angiogenic therapeutics is very low, and because little is known regarding the aberrant signaling that controls these tumors, personalized treatment options for many of these patients are lacking. In this review, we summarize several recent findings regarding the genomics of angiosarcomas, including new discoveries regarding aberrant angiogenic signaling and Myc amplification as key features of this tumor type.
血管肉瘤是极具侵袭性的罕见恶性肿瘤,起源于血管或淋巴管,主要发生在化学物质暴露或放射治疗之后。肿瘤对化疗、放疗或新型抗血管生成疗法的反应非常低,而且由于对控制这些肿瘤的异常信号传导了解甚少,许多此类患者缺乏个性化的治疗方案。在这篇综述中,我们总结了关于血管肉瘤基因组学的一些最新发现,包括关于异常血管生成信号传导和Myc扩增作为这种肿瘤类型关键特征的新发现。