Nrf2 缺陷促进黑色素瘤生长和肺转移

Reactive oxygen species (Apex, N.C.) Pub Date : 2016-01-01 Epub Date: 2016-05-30 DOI:10.20455/ros.2016.853
Hong Zhu, Zhenquan Jia, Michael A Trush, Y Robert Li
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引用次数: 0

摘要

Nrf2是抗氧化和细胞保护基因的关键调节因子,它在肿瘤发生中的作用仍存在争议。在这里,我们发现,小鼠皮下注射 B16-F10 黑色素瘤细胞后,Nrf2 缺乏会导致局部肿瘤生长增加,表现为局部可触及肿瘤肿块的动物比例增加,以及注射部位肿瘤体积随时间增加。体内生物发光成像也显示,与野生型小鼠相比,Nrf2-null 小鼠体内黑色素瘤的生长速度加快。通过使用高灵敏度的生物发光测定法,我们进一步发现,与野生型小鼠相比,Nrf2 缺失导致 B16-F10 黑色素瘤细胞的肺转移显著增加。综上所述,这篇短文的研究结果首次证明了小鼠皮下接种B16-F10细胞后,Nrf2缺乏会促进黑色素瘤的生长和肺转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Nrf2 Deficiency Promotes Melanoma Growth and Lung Metastasis.

Nrf2 Deficiency Promotes Melanoma Growth and Lung Metastasis.

Nrf2 Deficiency Promotes Melanoma Growth and Lung Metastasis.

Nrf2 Deficiency Promotes Melanoma Growth and Lung Metastasis.

The role of Nrf2, a key regulator of antioxidant and cytoprotective genes, in tumorigenesis remains controversial. Here we showed that Nrf2 deficiency led to increased local tumor growth in mice following subcutaneous injection of B16-F10 melanoma cells, as indicated by increased proportion of animals with locally palpable tumor mass and time-dependent increases in tumor volume at the injection site. In vivo bioluminescence imaging also revealed increased growth of melanoma in Nrf2-null mice as compared with wild-type mice. By using a highly sensitive bioluminometric assay, we further found that Nrf2 deficiency resulted in a remarkable increase in lung metastasis of B16-F10 melanoma cells as compared with wild-type mice. Taken together, the results of this short communication for the first time demonstrated that Nrf2 deficiency promoted melanoma growth and lung metastasis following subcutaneous inoculation of B16-F10 cells in mice.

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