IL-6 promotes malignant growth of skin SCCs by regulating a network of autocrine and paracrine cytokines

被引:111
作者
Lederle, Wiltrud [1 ,2 ]
Depner, Sofia [1 ]
Schnur, Sabine [1 ]
Obermueller, Eva [3 ]
Catone, Nicola [1 ]
Just, Alexandra [1 ]
Fusenig, Norbert E. [4 ]
Mueller, Margareta M. [1 ,5 ]
机构
[1] German Canc Res Ctr, Grp Tumor & Microenvironm, DKFZ ZMBH Alliance, D-69221 Heidelberg, Germany
[2] Rhein Westfal TH Aachen, Dept Expt Mol Imaging, Fac Med, Aachen, Germany
[3] Barts & London Queen Marys Sch Med & Dent, John Vane Sci Ctr, Translat Oncol Lab, London, England
[4] German Canc Res Ctr, Div Carcinogenesis & Differentiat, D-69221 Heidelberg, Germany
[5] HFU Furtwangen, Dept Mech & Proc Engn, Villigen, Switzerland
关键词
IL-6; cytokine network; MMP; tumor progression; COLONY-STIMULATING FACTOR; BREAST-CANCER CELLS; CARCINOMA-CELLS; IN-VIVO; TUMOR PROGRESSION; MULTIPLE-MYELOMA; STAT3; ACTIVATION; INTERLEUKIN-6; EXPRESSION; PROLIFERATION;
D O I
10.1002/ijc.25621
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cytokines play a crucial role in tumor initiation and progression. Here, we demonstrate that interleukin (IL)-6 is a key factor by driving tumor progression from benign to malignant, invasive tumors in the HaCaT-model of human skin carcinoma. IL-6 activates STAT3 and directly stimulates proliferation and migration of the benign noninvasive HaCaT-ras A-5 cells in vitro. Furthermore, IL-6 induces a complex, reciprocally regulated cytokine network in the tumor cells that includes inflammatory and angiogenic factors such as IL-8, GM-CSF, VEGF and MCP-1. These IL-6 effects lead to tumor cell invasion in organotypic cultures in vitro and to the formation of malignant and invasive s.c. tumors in vivo. Tumor invasion is supported by the IL-6 induced overexpression of MMP-1 in vitro and in vivo. These data demonstrate a key function of IL-6 in the progression of skin SCCs by regulating a complex cytokine and protease network and suggest new therapeutic approaches to target this central player in skin carcinogenesis.
引用
收藏
页码:2803 / 2814
页数:12
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