Wysoczynski Marcin, Ratajczak Mariusz Z
Stem Cell Biology Program at James Graham Brown Cancer Center, University of Louisville, Louisville, KY 40202, USA.
Int J Cancer. 2009 Oct 1;125(7):1595-603. doi: 10.1002/ijc.24479.
Microvesicles (MVs) are shed from cell membranes of several cell types and have an important function in cell-to-cell communication. Exponentially growing lung cancer cells secrete large quantities of MVs and we were interested in their role in tumor progression. We observed that both human and murine lung cancer cell lines secrete more MVs in response to non-apoptotic doses of hypoxia and irradiation. These tumor-derived (t)MVs activate and chemoattract stroma fibroblasts and endothelial cells. Furthermore, they induce expression of several pro-angiopoietic factors in stromal cells such as IL-8, VEGF, LIF, OSM, IL-11 and MMP-9. We also noticed that conditioned media harvested from stroma cells stimulated by tMVs enhanced the metastatic potential of both human and murine lung cancer cells in vivo. Thus, we postulated that tMVs are underappreciated constituents of the tumor microenvironment and play a pivotal role in tumor progression, metastasis and angiogenesis.
微泡(MVs)由多种细胞类型的细胞膜脱落形成,在细胞间通讯中发挥重要作用。指数生长的肺癌细胞分泌大量微泡,我们对其在肿瘤进展中的作用感兴趣。我们观察到,人和小鼠肺癌细胞系在非凋亡剂量的缺氧和辐射刺激下会分泌更多微泡。这些肿瘤来源的(t)微泡可激活并趋化基质成纤维细胞和内皮细胞。此外,它们可诱导基质细胞中多种促血管生成因子的表达,如白细胞介素-8(IL-8)、血管内皮生长因子(VEGF)、白血病抑制因子(LIF)、抑瘤素M(OSM)、白细胞介素-11(IL-11)和基质金属蛋白酶-9(MMP-9)。我们还注意到,由t微泡刺激的基质细胞收集的条件培养基可增强人和小鼠肺癌细胞在体内的转移潜能。因此,我们推测t微泡是肿瘤微环境中被低估的成分,在肿瘤进展、转移和血管生成中起关键作用。