Yu Ling, Guo Weichun, Zhao Shenghao, Wang Fuan, Xu Yong
Department of Orthopedics, Renmin Hospital of Wuhan University, Wuhan, Hubei, P.R. China.
Oncol Lett. 2011 Nov;2(6):1083-1087. doi: 10.3892/ol.2011.363. Epub 2011 Jul 14.
Communication between cancer cells and the microenvironment appears to be an important determinant of disease prognosis. However, the detailed mechanisms of the interactions between cancer cells and surrounding cells have yet to be clarified. Recent studies on cell fusion have indicated this interaction to be one of the driving forces in cancer progression. Fibroblasts constitute a significant component of the carcinoma stromal compartment. Many of these fibroblasts are thought to differentiate into myofibroblasts, which are characterized by a positive expression of α-smooth muscle actin. Expression of α-smooth muscle actin in osteosarcoma was evaluated, and was observed to be excessive in the multinucleated osteoclast-like giant cells in osteosarcoma tissue, indicating the possibility of cell fusion between cancer cells and myofibroblasts. In order to test the above hypothesis, we first transformed the primary mouse embryonic fibroblast cells into activated myofibroblast cells. Osteosarcoma cells were then co-cultured with mouse myofibroblast cells, and cell fusion was investigated using species-specific chromosomal markers. Expression of α-smooth muscle actin was successfully induced in primary mouse embryonic fibroblast cells. Cells fused spontaneously with a fusion rate of approximately 1-2% and fusion between more than two cells was also observed. Our study demonstrated that fusion between cancer cells and myofibroblasts may contribute to the observed multinucleated giant cells in osteosarcoma. We posit that cell fusion is a novel mechanism for the interaction between cancer cells and the microenvironment.
癌细胞与微环境之间的通讯似乎是疾病预后的一个重要决定因素。然而,癌细胞与周围细胞之间相互作用的详细机制尚未阐明。最近关于细胞融合的研究表明,这种相互作用是癌症进展的驱动力之一。成纤维细胞是癌基质成分的重要组成部分。这些成纤维细胞中的许多被认为会分化为肌成纤维细胞,其特征是α-平滑肌肌动蛋白呈阳性表达。对骨肉瘤中α-平滑肌肌动蛋白的表达进行了评估,发现其在骨肉瘤组织中的多核破骨细胞样巨细胞中过度表达,这表明癌细胞与肌成纤维细胞之间可能发生了细胞融合。为了验证上述假设,我们首先将原代小鼠胚胎成纤维细胞转化为活化的肌成纤维细胞。然后将骨肉瘤细胞与小鼠肌成纤维细胞共培养,并使用物种特异性染色体标记物研究细胞融合情况。在原代小鼠胚胎成纤维细胞中成功诱导了α-平滑肌肌动蛋白的表达。细胞自发融合,融合率约为1%-2%,并且还观察到了两个以上细胞之间的融合。我们的研究表明,癌细胞与肌成纤维细胞之间的融合可能导致了骨肉瘤中观察到的多核巨细胞的形成。我们认为细胞融合是癌细胞与微环境之间相互作用的一种新机制。