Genomic gain and over expression of CCL2 correlate with vascular invasion in stage I non-seminomatous testicular germ-cell tumours.

Details

Serval ID
serval:BIB_D618D01B06EA
Type
Article: article from journal or magazin.
Collection
Publications
Title
Genomic gain and over expression of CCL2 correlate with vascular invasion in stage I non-seminomatous testicular germ-cell tumours.
Journal
International journal of andrology
Author(s)
Gilbert D.C., Chandler I., Summersgill B., McIntyre A., Missiaglia E., Goddard N.C., Huddart R.A., Shipley J.
ISSN
1365-2605 (Electronic)
ISSN-L
0105-6263
Publication state
Published
Issued date
08/2011
Peer-reviewed
Oui
Volume
34
Number
4 Pt 2
Pages
e114-21; discussion e121
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Abstract
Testicular germ-cell tumours (TGCT) are the most frequent solid tumour to affect young Caucasian adult males and have increased in incidence over recent decades. In clinical stage I non-seminomas, (NSGCT) histological vascular invasion (VI) is a prognostic factor for metastatic relapse. Using array comparative genomic hybridization, we have previously shown that the presence of VI is associated with gain of a region at 17q12, containing a cluster of genes encoding inflammatory cytokines. We here confirm this finding using fluorescence in situ hybridization (FISH) demonstrating gain in 12 out of 42 (29%) assessable samples. Interrogation of previously published expression microarray data suggests that of the genes contained within this region, CCL2 [monocyte chemoattractant protein 1 (MCP1)] is frequently overexpressed in TGCT. Immunohistochemistry confirms this finding in a collection of 67 clinical stage I NSGCT, demonstrating an association with the presence of VI (p=0.049) that was not seen with VEGF-A, MMP2 or MMP9, although all were frequently expressed. This work gives further insight into the mechanisms involved in invasion in this tumour type, which may ultimately have implications for the management of patients with stage I disease.
Keywords
Adolescent, Adult, Biomarkers, Tumor/biosynthesis, Chemokine CCL2/biosynthesis, Chromosomes, Human, Pair 17/genetics, Genome, Human, Humans, In Situ Hybridization, Fluorescence, Male, Matrix Metalloproteinase 2/biosynthesis, Matrix Metalloproteinase 9/biosynthesis, Middle Aged, Neoplasm Staging, Neoplasms, Germ Cell and Embryonal/blood supply, Neoplasms, Germ Cell and Embryonal/metabolism, Neoplasms, Germ Cell and Embryonal/pathology, Neovascularization, Pathologic, Oligonucleotide Array Sequence Analysis, Prognosis, Testicular Neoplasms/blood supply, Testicular Neoplasms/metabolism, Testicular Neoplasms/pathology, Vascular Endothelial Growth Factor A/biosynthesis
Pubmed
Web of science
Create date
26/09/2023 9:53
Last modification date
04/10/2023 14:27
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