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血管生成标志物在喉癌中的潜在预后及治疗作用

Potential prognostic and therapeutic role for angiogenesis markers in laryngeal carcinoma.

作者信息

Lionello Marco, Staffieri Alberto, Marioni Gino

机构信息

Department of Neurosciences, Otolaryngology Section, University of Padova, Padova, Italy.

出版信息

Acta Otolaryngol. 2012 Jun;132(6):574-82. doi: 10.3109/00016489.2011.652308. Epub 2012 Apr 12.

Abstract

Angiogenesis is a hallmark of cancer, fundamental to its growth. The 'angiogenic switch' occurs when pro-angiogenic factors are not balanced by anti-angiogenic factors. A correlation between angiogenic properties and oncological prognosis (for laryngeal squamous cell carcinoma (LSCC) too) was first hypothesized in the 1990s. An exhaustive literature review was performed to investigate available data on angiogenesis markers and their biological role and therapeutic potential in LSCC. The prognostic significance of microvascular density in LSCC was investigated with endothelial targets, e.g. CD105, CD34, and CD31. Epidermal growth factor receptor (EGFR), vascular endothelial growth factor (VEGF), VEGF receptor 2, angiogenin, hypoxia-inducible factor 1, and other biological markers were also studied. Only anti-EGFR therapy has been approved by the USFood and Drug Administration (FDA) for head and neck carcinoma in recent years, while several agents interfering with VEGF and its receptors are being studied. Experimental findings indicate that anti-CD105 monoclonal antibodies efficiently inhibit tumor angiogenesis. There are two main ways to approach the vascular profile of solid malignancies: by inhibiting new vessel formation (anti-angiogenic therapy) or selectively damaging neoplastic vessels (vascular targeting therapy). In advanced LSCC, both these strategies seem promising and warrant further preclinical and clinical investigation.

摘要

血管生成是癌症的一个标志,对其生长至关重要。当促血管生成因子与抗血管生成因子失衡时,就会发生“血管生成开关”。血管生成特性与肿瘤预后之间的相关性(对喉鳞状细胞癌(LSCC)也是如此)最早在20世纪90年代被提出。进行了详尽的文献综述,以研究关于血管生成标志物及其在LSCC中的生物学作用和治疗潜力的现有数据。通过内皮靶点,如CD105、CD34和CD31,研究了LSCC中微血管密度的预后意义。还研究了表皮生长因子受体(EGFR)、血管内皮生长因子(VEGF)、VEGF受体2、血管生成素、缺氧诱导因子1和其他生物学标志物。近年来,只有抗EGFR疗法已被美国食品药品监督管理局(FDA)批准用于头颈癌,而几种干扰VEGF及其受体的药物正在研究中。实验结果表明,抗CD105单克隆抗体能有效抑制肿瘤血管生成。针对实体恶性肿瘤血管特征有两种主要方法:通过抑制新血管形成(抗血管生成疗法)或选择性破坏肿瘤血管(血管靶向疗法)。在晚期LSCC中,这两种策略似乎都很有前景,值得进一步进行临床前和临床研究。

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