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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Angiogenic switch during tumor progression of carcinoma ex-pleomorphic adenoma

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Author(s):
Soares, A. B. ; Juliano, P. B. ; Araujo, V. C. [3] ; Metze, K. ; Altemani, A.
Total Authors: 5
Document type: Journal article
Source: Virchows Archiv; v. 451, n. 1, p. 65-71, July 2007.
Field of knowledge: Health Sciences - Medicine
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. (AU)

FAPESP's process: 04/07960-0 - Study of alterations occurred in the adenoma during the process of malignization in ex-adenoma pleomorphic carcinoma
Grantee:Vera Cavalcanti de Araujo
Support Opportunities: Research Projects - Thematic Grants