Department of Biochemical Sciences, University of Florence, Tuscany, Italy.
Cancer Res. 2010 Sep 1;70(17):6945-56. doi: 10.1158/0008-5472.CAN-10-0785. Epub 2010 Aug 10.
Although cancer-associated fibroblasts (CAF) are key determinants in the malignant progression of cancer, their functional contribution to this process is still unclear. Analysis of the mutual interplay between prostate carcinoma cells and CAFs revealed a mandatory role of carcinoma-derived interleukin-6 in fibroblast activation. In turn, activated fibroblasts through secretion of metalloproteinases elicit in cancer cells a clear epithelial-mesenchymal transition (EMT), as well as enhancement of tumor growth and development of spontaneous metastases. CAF-induced EMT leads prostate carcinoma cells to enhance expression of stem cell markers, as well as the ability to form prostaspheres and to self-renew. Hence, the paracrine interplay between CAFs and cancer cells leads to an EMT-driven gain of cancer stem cell properties associated with aggressiveness and metastatic spread.
尽管癌症相关成纤维细胞(CAF)是癌症恶性进展的关键决定因素,但它们对这一过程的功能贡献仍不清楚。分析前列腺癌细胞与 CAF 之间的相互作用,揭示了癌源性白细胞介素 6 在成纤维细胞激活中的必需作用。反过来,激活的成纤维细胞通过分泌金属蛋白酶,在癌细胞中引发明显的上皮-间充质转化(EMT),以及增强肿瘤生长和自发转移的发展。CAF 诱导的 EMT 导致前列腺癌细胞增强干细胞标志物的表达,以及形成前列腺球体和自我更新的能力。因此,CAF 和癌细胞之间的旁分泌相互作用导致 EMT 驱动的获得与侵袭性和转移扩散相关的癌症干细胞特性。