Stromal fibroblasts synergize with hypoxic oxidative stress to enhance melanoma aggressiveness

被引:43
作者
Comito, Giuseppina
Giannoni, Elisa
Di Gennaro, Paola
Segura, Coral Pons
Gerlini, Gianni
Chiarugi, Paola [1 ]
机构
[1] Univ Florence, Dept Biochem Sci, Tuscany Tumor Inst, I-50134 Florence, Italy
关键词
Melanoma; Stromal fibroblast; Hypoxia; IL-6; VEGF; EPITHELIAL-MESENCHYMAL TRANSITION; CARCINOMA-ASSOCIATED FIBROBLASTS; TUMOR MICROENVIRONMENT; STEM-CELLS; MOLECULAR CHARACTERIZATION; IN-VIVO; CANCER; PROGRESSION; GROWTH; MYOFIBROBLAST;
D O I
10.1016/j.canlet.2012.04.025
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
On the basis of recent advances indicating a key role of microenvironment for tumor progression, we investigated the role of fibroblasts, macrophages and hypoxia, for primary melanoma aggressiveness. Our data indicate a key role of hypoxia in stromal reactivity, acting on both myofibroblasts and machrophages differentiation. Hypoxic myofibroblasts are more active than macrophages in inducing melanoma invasiveness and exploit their oxidative stress due to hypoxia to secrete soluble factors favouring melanoma invasion and chemotaxis. We underscore the key role of microenviroment on melanoma malignancy, highlighting reactive fibroblasts, intratumoral hypoxia and oxidative stress as promising targets for melanoma antimetastatic strategies. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:31 / 41
页数:11
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