Title of article
A translocation involving the placental growth factor gene is identified in an epithelioid hemangioendothelioma
Author/Authors
He، نويسنده , , Mai and Das، نويسنده , , Kasturi and Blacksin، نويسنده , , Marcia and Benevenia، نويسنده , , Joseph and Hameed، نويسنده , , Meera، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2006
Pages
5
From page
150
To page
154
Abstract
Hemangioendothelioma is a relatively rare vascular tumor that is considered a low- to intermediate-grade malignant neoplasm. Cytogenetic reports of hemangioendothelioma are rare. Two reports with translocations involving chromosomes 1 and 3 have been described. Here we report a case of an epithelioid hemangioendothelioma arising in the foot of a 56-year-old female, with a 46,XX,-6,t(10;14)(p13;q24),+r. The regions in 10p13 and 14q24 encompass genes that participate in growth regulation. One of the genes at 14q24 encodes for placental growth factor [PlGF, also called vascular endothelial growth factor (VEGF)-related protein]. Placental growth factor is a member of the VEGF growth factor family. Placenta growth factor binds only to VEGF receptor-1 (FLT-1). It has been suggested that PlGF may modulate VEGF-induced angiogenesis by the formation of PlGF/VEGF heterodimers in cells producing both factors. It has been postulated that PlGF is involved in intra- and intermolecular cross-talk between VEGF receptor-1 (FLT) and receptor-2 (FLK-1/KDR). Since expression of VEGF and its receptor, FLK-1, is seen in several cases of epithelioid hemangioendothelioma and plasma VEGF level is also used to follow-up this tumor, we performed immunohistochemical analysis for PlGF and VEGF in our case. The strong positivity for both PlGF and VEGF observed in our case implies that the t(10;14)(p13;q24) most likely involves PlGF, which may be one of the genes driving oncogenesis in these tumors.
Journal title
Cancer Genetics and Cytogenetics
Serial Year
2006
Journal title
Cancer Genetics and Cytogenetics
Record number
1827740
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