Department of Pathology, University of Ioannina, Ioannina, Greece.
Department of Ophthalmology, University of Ioannina, Ioannina, Greece.
Anticancer Res. 2014 Sep;34(9):4977-83.
BACKGROUND/AIM: Tumor angiogenesis has been the subject of intensive research in recent years in many tumor types. Studies involving epithelial skin tumors are few to date. We evaluated tumor angiogenesis and lymphangiogenesis in cancerous and pre-cancerous lesions of the eyelids using immunohistochemical techniques.
The study included 147 formalin-fixed, paraffin-embedded samples. We studied cancerous lesions of the eyelid skin such as basal cell carcinoma, squamous and basosquamous cell carcinoma and pre-cancerous lesions such as actinic keratosis and Bowen's disease. We applied immunohistochemical staining using antibodies to investigate angiogenic and lymphangiogenic molecular factors, such as vascular endothelial growth factor (VEGF) and its receptors. We recorded the microvascular density of these tumors by using the marker CD-105, a specific antibody against endoglin protein.
Data analysis showed that the molecular factors that control angiogenesis are expressed in high proportions in the tumors studied and that this expression is positively-correlated with tumor microvascular density. Furthermore, correlations emerged with the mean diameter of these tumors. We also found differences in microvascular density between pre-cancerous and cancerous eyelid lesions.
Activation of the angiogenic molecular factors results in intratumoral and peritumoral microvascularity formation at initial tumor growth. As the tumor attains a certain size and microvascular network, some VEGF receptors appear to decrease. Tumor angiogenesis appears to be active in cutaneous malignancies of the eyelids; therefore our hypothesis of a potential anti-angiogenic therapy for the studied tumors needs investigation in future studies.
背景/目的:近年来,在许多肿瘤类型中,肿瘤血管生成已成为研究热点。目前涉及上皮皮肤肿瘤的研究很少。我们使用免疫组织化学技术评估了眼睑癌性和癌前病变中的肿瘤血管生成和淋巴管生成。
本研究包括 147 例福尔马林固定、石蜡包埋的样本。我们研究了眼睑皮肤的癌性病变,如基底细胞癌、鳞状细胞癌和基底鳞状细胞癌,以及癌前病变,如光化性角化病和 Bowen 病。我们应用免疫组织化学染色,使用针对血管内皮生长因子(VEGF)及其受体等血管生成和淋巴管生成分子因子的抗体进行研究。我们通过使用标记物 CD-105(针对内皮糖蛋白的特异性抗体)记录这些肿瘤的微血管密度。
数据分析表明,控制血管生成的分子因子在研究的肿瘤中以高比例表达,并且这种表达与肿瘤微血管密度呈正相关。此外,还与这些肿瘤的平均直径相关。我们还发现了癌前和癌性眼睑病变之间的微血管密度差异。
血管生成分子因子的激活导致肿瘤内和肿瘤周围微血管形成在初始肿瘤生长时。随着肿瘤达到一定的大小和微血管网络,一些 VEGF 受体似乎减少。眼睑皮肤恶性肿瘤中的肿瘤血管生成似乎是活跃的;因此,我们对研究肿瘤进行潜在抗血管生成治疗的假设需要在未来的研究中进行调查。