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NAD(P)H:醌氧化还原酶 1 诱导黑素瘤细胞的细胞周期进程和增殖。

The NAD(P)H:Quinone Oxidoreductase 1 induces cell cycle progression and proliferation of melanoma cells.

机构信息

Department of Dermatology and Skin Science, Jack Bell Research Centre, Vancouver Coastal Health Research Institute, University of British Columbia, Vancouver, BC Canada.

出版信息

Free Radic Biol Med. 2010 Jun 15;48(12):1601-9. doi: 10.1016/j.freeradbiomed.2010.03.003. Epub 2010 Mar 11.

Abstract

The oxidoreductase NQO1 plays a prominent role in maintaining the cellular homeostasis. NQO1 is mainly a cytosolic enzyme which catalyzes the metabolism of quinones and is present in almost all tissue types providing protection against different stresses including xenobiotics, oxidants, UV light, and ionizing radiation. This enzyme is overexpressed in many cancerous tissues and its function in carcinogenesis remains unclear. Due to the relative lack of information on the role of NQO1 in melanoma pathogenesis, we attempted to determine the expression and basic function of NQO1 in melanoma cell proliferation. We found that NQO1 is overexpressed in most melanoma cell lines with respect to melanocytes. Furthermore, the expression of this oxidoreductase significantly induces cell cycle progression by upregulating the expression of cyclins A2, B1 and D1, leading to the proliferation of melanoma cells. Our results also indicate that NQO1 is an upstream regulator of NF-kappaB p50, a factor linked to melanoma progression and poor patient prognosis. Interestingly, we found that NQO1 stabilizes the transactivator BCL3, which in turn upregulates NF-kappaB p50. More importantly, our results also indicate that NF-kappaB p50 correlates with the expression of NQO1 and mediates its role in the proliferation of melanoma cells.

摘要

氧化还原酶 NQO1 在维持细胞内稳态方面发挥着重要作用。NQO1 主要是一种细胞溶质酶,可催化醌类的代谢,几乎存在于所有组织类型中,为抵御包括异源物、氧化剂、UV 光和电离辐射在内的各种应激提供保护。这种酶在许多癌组织中过度表达,其在致癌作用中的功能尚不清楚。由于关于 NQO1 在黑色素瘤发病机制中的作用的信息相对较少,我们试图确定 NQO1 在黑色素瘤细胞增殖中的表达和基本功能。我们发现,与黑色素细胞相比,NQO1 在大多数黑色素瘤细胞系中过度表达。此外,这种氧化还原酶的表达通过上调细胞周期蛋白 A2、B1 和 D1 的表达,显著诱导细胞周期进程,导致黑色素瘤细胞增殖。我们的结果还表明,NQO1 是 NF-κB p50 的上游调节剂,NF-κB p50 与黑色素瘤的进展和患者预后不良有关。有趣的是,我们发现 NQO1 稳定了转录激活因子 BCL3,从而上调了 NF-κB p50。更重要的是,我们的结果还表明,NF-κB p50 与 NQO1 的表达相关,并介导其在黑色素瘤细胞增殖中的作用。

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