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A strategy for the suppression of tumorigenesis induced by biomaterials: Restoration of transformed phenotype of polyetherurethane-induced tumor cells by Cx43 transfection

机译:抑制生物材料诱导的肿瘤发生的策略:通过Cx43转染恢复聚醚氨酯诱导的肿瘤细胞的转化表型

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摘要

Biomaterials such as polyetherurethans (PEUs) are the scaffolding, which is indispensable for the development of the bio-artificial organs. However, PEUs can induce tumors in subcutaneous implantation sites in rat. We have shown that the different inhibitory potential of gap junctional intercellular communication (GJIC) on the surface of the biomaterials, including PEUs, is a key step in determining the tumorigenic potential. Here we show that suppression of a gap junctional protein connexin 43 (Cx43) plays an important role in in vivo tumorigenesis induced by PEUs for the first time and that Cx43 transfection may be an effective strategy for preventing tumorigenesis induced by biomaterials. Rat tumor cell line U41 is derived from tumors in the subcutaneous implantation of PEU films. The GJIC and the expression of Cx43 were suppressed in U41. The restoration of normal phenotype, such as reduction of growth rate, recovery of contact inhibition and loss of colony formation ability in soft agar, was achieved by Cx43 transfection. These results strongly suggest that suppression of Cx43 expression plays an important role in the development of rat malignant fibrous histiocytoma (MFHC) caused by PEUs and that Cx43 transfection is effective for prevention of tumorigenesis induced by PEUs.
机译:诸如聚醚脲(PEUs)之类的生物材料是支架,这对于生物人工器官的发展是必不可少的。但是,PEU可以在大鼠皮下植入部位诱发肿瘤。我们已经表明,在包括PEU在内的生物材料表面上,间隙连接细胞间通讯(GJIC)的不同抑制潜力是确定致瘤潜力的关键步骤。在这里,我们显示抑制间隙连接蛋白连接蛋白43(Cx43)首次在PEUs诱导的体内肿瘤发生中起重要作用,并且Cx43转染可能是预防由生物材料引起的肿瘤发生的有效策略。大鼠肿瘤细胞系U41源自PEU膜皮下植入中的肿瘤。在U41中,GJIC和Cx43的表达受到抑制。通过Cx43转染可恢复正常表型,例如降低生长速度,恢复接触抑制和丧失软琼脂中的菌落形成能力。这些结果强烈表明,抑制Cx43表达在由PEU引起的大鼠恶性纤维组织细胞瘤(MFHC)的发展中起重要作用,并且Cx43转染对于预防由PEU诱导的肿瘤发生有效。

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