Regulation of pathological lymphangiogenesis requires factors distinct from those governing physiological lymphangiogenesis

被引:12
|
作者
Hirakawa, Satoshi [1 ,2 ]
机构
[1] Ehime Univ, Grad Sch Med, Dept Dermatol, Toon, Ehime 7910295, Japan
[2] Ehime Univ, Ehime Proteomed Res Ctr, Dept Cell Growth & Tumor Regulat, Toon, Ehime 7910295, Japan
关键词
Angiogenesis; Metastasis; Tumor progression; Vascular endothelial growth factor; Vascular development; GROWTH-FACTOR-C; LYMPH-NODE METASTASIS; ENDOTHELIAL PROGENITOR CELLS; PROMOTES TUMOR-METASTASIS; CHRONIC SKIN INFLAMMATION; BREAST-CANCER METASTASIS; MELANOMA METASTASIS; VESSEL FORMATION; CD11B(+) MACROPHAGES; RECEPTOR CLEC-2;
D O I
10.1016/j.jdermsci.2010.11.020
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Physiological lymphangiogenesis requires key factors such as vascular endothelial growth factor (VEGF)C and the homeodomain transcription factor Prox1 to induce the formation of primitive lymph sacs from veins during mammalian development. However, pathological lymphangiogenesis, defined as new lymphatic vessel growth resulting from pathogenic stimuli, may utilize additional signaling pathways and/or cell types in conditions such as tumor progression or inflammatory responses. In fact, although both physiological and pathological lymphatic vascular development share fundamental mechanisms, pleiotropic growth factors and/or pro-inflammatory cytokines mediate lymphangiogenesis in experimental models of pathologic lymphangiogenesis. This review summarizes molecular mechanisms underlying lymphangiogenesis in pathological conditions and focuses in particular on current findings relevant to tumor-associated lymphangiogenesis. (C) 2010 Japanese Society for Investigative Dermatology. Published by Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:85 / 93
页数:9
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