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癌性多形性腺瘤肿瘤进展过程中的血管生成开关

Angiogenic switch during tumor progression of carcinoma ex-pleomorphic adenoma.

作者信息

Soares A B, Juliano P B, Araujo V C, Metze K, Altemani A

机构信息

Department of Pathology, Medical Science Faculty, University of Campinas, Campinas, SP, Brazil.

出版信息

Virchows Arch. 2007 Jul;451(1):65-71. doi: 10.1007/s00428-007-0438-z. Epub 2007 Jun 26.

DOI:10.1007/s00428-007-0438-z
PMID:17593387
Abstract

We analyzed the tumor vascularization in carcinomas ex-pleomorphic adenoma (CXPA) to investigate the angiogenic switch during the malignant transformation of pleomorphic adenoma (PA) to carcinoma and during tumor progression. In eight cases of early CXPA (intracapsular and minimally invasive tumors), eight of advanced CXPA (widely invasive tumors), and ten of PA without malignant transformation, tumor vascularization was assessed in histological samples by measuring total microvascular area (TVA) and microvessel density (MVD) using CD34 and CD105 antibodies. MVD for CD105 increased significantly during tumor progression, whereas this was not the case for CD34 MVD. Comparing widely invasive CXPA with and without myoepithelial differentiation, CXPA with myoepithelial differentiation showed a significantly lower number of CD105 positive vessels but revealed higher TVA values. In these tumors, the neoplastic cells usually formed larger hypovascularized aggregates that were often surrounded by large-sized vessels. In conclusion, the antibody CD105 reveals an angiogenic switch during the progression from adenoma to carcinoma in salivary glands. The degree of angiogenesis and the total vascular area have distinctive patterns in CXPA with and without myoepithelial differentiation. Low angiogenesis associated with high TVA value is more characteristic of CXPA with myoepithelial differentiation.

摘要

我们分析了多形性腺瘤癌变(CXPA)中的肿瘤血管生成情况,以研究多形性腺瘤(PA)向癌恶性转化过程以及肿瘤进展过程中的血管生成开关。在8例早期CXPA(囊内及微侵袭性肿瘤)、8例晚期CXPA(广泛侵袭性肿瘤)以及10例未发生恶性转化的PA中,通过使用CD34和CD105抗体测量组织学样本中的总微血管面积(TVA)和微血管密度(MVD)来评估肿瘤血管生成情况。CD105的MVD在肿瘤进展过程中显著增加,而CD34的MVD则不然。比较有和没有肌上皮分化的广泛侵袭性CXPA,有肌上皮分化的CXPA显示CD105阳性血管数量显著减少,但TVA值更高。在这些肿瘤中,肿瘤细胞通常形成较大的低血管化聚集体,这些聚集体常被大尺寸血管包围。总之,抗体CD105揭示了唾液腺腺瘤向癌进展过程中的血管生成开关。有和没有肌上皮分化的CXPA中血管生成程度和总血管面积具有不同模式。低血管生成与高TVA值相关是有肌上皮分化的CXPA的更典型特征。

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