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Inhibition of cell growth by overexpression of manganese superoxide dismutase (MnSOD) in human pancreatic carcinoma.

机译:过度表达锰超氧化物歧化酶(MnSOD)在人胰腺癌中抑制细胞生长。

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Manganese superoxide dismutase (MnSOD) levels have been found to be low in human pancreatic cancer [Pancreas 26, (2003), 23] and human pancreatic cancer cell lines [Cancer Res. 63, (2003), 1297] when compared to normal human pancreas. We hypothesized that stable overexpression of pancreatic cancer cells with MnSOD cDNA would alter the malignant phenotype. MIA PaCa-2 cells were stably transfected with a pcDNA3 plasmid containing sense human MnSOD cDNA or containing no MnSOD insert by using the lipofectAMINE method. G418-resistant colonies were isolated, grown and maintained. Overexpression of MnSOD was confirmed in two selected clones with a 2-4-fold increase in MnSOD immunoreactive protein. Compared with the parental and neo control cells, the MnSOD-overexpressing clones had decreased growth rates, growth in soft agar and plating efficiency in vitro, while in vivo, the MnSOD-overexpressing clones had slower growth in nude mice. These results suggest that MnSOD may be a tumor suppressor gene in human pancreatic cancer.
机译:已发现在人胰腺癌[Pancreas 26,(2003),23]和人胰腺癌细胞系[Cancer Res.Med.Res.Med.Sci。,2003,6,3]中锰超氧化物歧化酶(MnSOD)水平低。 63,(2003),1297]与正常人胰腺相比。我们假设具有MnSOD cDNA的胰腺癌细胞的稳定过表达将改变恶性表型。使用lipofectAMINE方法,用含有正义人MnSOD cDNA或不含MnSOD插入片段的pcDNA3质粒稳定转染MIA PaCa-2细胞。分离,生长和维持G418抗性菌落。在两个选定的克隆中证实了MnSOD的过表达,其中MnSOD免疫反应蛋白增加了2-4倍。与亲本和新对照细胞相比,过表达MnSOD的克隆在体外具有降低的生长速率,在软琼脂中的生长和铺板效率,而在体内,过表达MnSOD的克隆在裸鼠中具有较慢的生长。这些结果表明,MnSOD可能是人胰腺癌的抑癌基因。

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