Augsten Martin, Hägglöf Christina, Olsson Eleonor, Stolz Claudia, Tsagozis Panagiotis, Levchenko Tetyana, Frederick Mitchell J, Borg Ake, Micke Patrick, Egevad Lars, Ostman Arne
Department of Oncology-Pathology, Karolinska Institutet, 171 76 Stockholm, Sweden.
Proc Natl Acad Sci U S A. 2009 Mar 3;106(9):3414-9. doi: 10.1073/pnas.0813144106. Epub 2009 Feb 13.
This study explored the role of secreted fibroblast-derived factors in prostate cancer growth. Analyses of matched normal and tumor tissue revealed up-regulation of CXCL14 in cancer-associated fibroblasts of a majority of prostate cancer. Fibroblasts over-expressing CXCL14 promoted the growth of prostate cancer xenografts, and increased tumor angiogenesis and macrophage infiltration. Mechanistic studies demonstrated that autocrine CXCL14-stimulation of fibroblasts stimulate migration and ERK-dependent proliferation of fibroblasts. CXCL14-stimulation of monocyte migration was also demonstrated. Furthermore, CXCL14-producing fibroblasts, but not recombinant CXCL14, enhanced in vitro proliferation and migration of prostate cancer cells and in vivo angiogenesis. These studies thus identify CXCL14 as a novel autocrine stimulator of fibroblast growth and migration, with multi-modal tumor-stimulatory activities. In more general terms, our findings suggest autocrine stimulation of fibroblasts as a previously unrecognized mechanism for chemokine-mediated stimulation of tumor growth, and suggest a novel mechanism whereby cancer-associated fibroblasts achieve their pro-tumorigenic phenotype.
本研究探讨了分泌型成纤维细胞衍生因子在前列腺癌生长中的作用。对配对的正常组织和肿瘤组织进行分析发现,大多数前列腺癌的癌相关成纤维细胞中CXCL14上调。过表达CXCL14的成纤维细胞促进前列腺癌异种移植瘤的生长,并增加肿瘤血管生成和巨噬细胞浸润。机制研究表明,成纤维细胞的自分泌CXCL14刺激可促进成纤维细胞的迁移和ERK依赖性增殖。还证实了CXCL14刺激单核细胞迁移。此外,产生CXCL14的成纤维细胞而非重组CXCL14增强了前列腺癌细胞的体外增殖和迁移以及体内血管生成。因此,这些研究确定CXCL14是一种新型的成纤维细胞生长和迁移自分泌刺激因子,具有多模式肿瘤刺激活性。更一般地说,我们的研究结果表明成纤维细胞的自分泌刺激是趋化因子介导的肿瘤生长刺激的一种先前未被认识的机制,并提示了一种癌相关成纤维细胞获得其促肿瘤表型的新机制。