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play <strong>an</strong> import<strong>an</strong>t role in <strong>an</strong>giogenesis. G<strong>as</strong>troenterop<strong>an</strong>creatic neuroendocrine<br />

tumors (GEP-NETs) are rare <strong>an</strong>d heterogeneous. Although markers for GEP-<br />

NETs exist, sensitive <strong>an</strong>d specific markers that indicate tumor <strong>growth</strong> <strong>an</strong>d behavior<br />

are lacking.<br />

Research frontiers<br />

The aim <strong>of</strong> the present study w<strong>as</strong> to evaluate the expression <strong>an</strong>d potential<br />

prognostic role <strong>of</strong> VEGF <strong>an</strong>d endoglin in GEP-NETs.<br />

Innovations <strong>an</strong>d breakthroughs<br />

From other studies it is already known that GEP-NETs are highly v<strong>as</strong>cularized<br />

tumors. Although several studies have investigated the immunohistochemical<br />

expression VEGF in GEP-NETs, VEGF <strong>tissue</strong> levels or endoglin expression<br />

have not been studied in these tumors before. Therefore, this study is believed<br />

to be the first to investigate <strong>tissue</strong> expression <strong>an</strong>d levels <strong>of</strong> VEGF <strong>an</strong>d endoglin<br />

in GEP-NETs, to determine the clinical impact <strong>of</strong> these <strong>an</strong>giogenic <strong>factor</strong>s in<br />

patients with GEP-NETs.<br />

Applications<br />

B<strong>as</strong>ed on our findings, we suggest that endoglin is a potential marker to indicate<br />

the presence <strong>of</strong> met<strong>as</strong>t<strong>as</strong>es in GEP-NETs. By demonstrating that incre<strong>as</strong>ed<br />

endoglin expression on tumors is related to tumor aggressiveness (including<br />

grade <strong>of</strong> differentiation, size <strong>an</strong>d presence <strong>of</strong> met<strong>as</strong>t<strong>as</strong>es), this study could present<br />

a future target for post-resection therapeutic intervention in the treatment <strong>of</strong><br />

patients with GEP-NETs.<br />

Terminology<br />

Angiogenesis is the process <strong>of</strong> new blood vessel formation. This process is induced<br />

by several <strong>growth</strong> <strong>factor</strong>s, including VEGF, <strong>an</strong>d tr<strong>an</strong>sforming <strong>growth</strong> <strong>factor</strong><br />

(TGF)-β1. Endoglin is a co-receptor for TGF-β1 <strong>an</strong>d a marker for <strong>an</strong>giogenic<br />

endothelial cells.<br />

Peer review<br />

This is a well-written paper that describes a study that evaluated the expression<br />

<strong>an</strong>d potential prognostic role <strong>of</strong> VEGF <strong>an</strong>d endoglin in a small sample <strong>of</strong> GEP-<br />

NETs patients, <strong>an</strong>d is <strong>of</strong> considerable interest.<br />

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S- Editor Sun H L- Editor Kerr C E- Editor Zheng XM<br />

225 J<strong>an</strong>uary 14, 2011|Volume 17|Issue 2|

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