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AP-1——Jun 蛋白:伪装的癌基因还是抑癌基因?

AP-1--The Jun proteins: Oncogenes or tumor suppressors in disguise?

机构信息

Department of Biochemistry and Molecular Biology, The Institute for Medical Research-Israel-Canada, The Hebrew University-Hadassah Medical School, Jerusalem, Israel.

出版信息

Cell Signal. 2010 Jun;22(6):894-9. doi: 10.1016/j.cellsig.2009.12.008. Epub 2010 Jan 11.

Abstract

Since its discovery more than two decades ago the involvement of the Activating protein 1 (AP-1) in proliferation, inflammation, differentiation, apoptosis, cellular migration and wound healing has been intensively studied. A model based on the early studies suggested antagonistic roles for the Jun proteins in proliferation and transformation. c-Jun was suggested to enhance transformation whereas JunB suggested to inhibit it in an antagonistic manner. Surprisingly, despite accumulation of data obtained from animal models regarding the role of Jun proteins in cancer and identification of oncogenic pathways regulating them, their involvement in human cancer was not demonstrated until recently. Here, we will describe the current knowledge about the roles of Jun proteins in human neoplasia. We will focus on the pathological examples demonstrating that the initial dogma has to be reexamined. For example, like c-Jun, JunB seems to play an oncogenic role in lymphomas, particularly in Hodgkin's lympomas. Furthermore, unlike the antagonistic activities of c-Jun and JunB in the transcription of genes coding for major cell cycle regulators such as CyclinD or p16INK4A, the transcription of other cell cycle regulating genes is modified similarly by c-Jun or JunB. Interestingly, some of these genes such as the ones coding for CyclinA or p19(ARF) are important players in either positive or negative regulation of cellular proliferation and survival. Finally, we will also discuss results posing JNK, known so far as the major activator of c-Jun, as a negative regulator of c-Jun level and activity. These recent findings suggest that the role of each Jun protein in neoplasia as well as in cellular survival should be examined in a context-dependent manner.

摘要

自二十多年前发现以来,激活蛋白 1(AP-1)在增殖、炎症、分化、凋亡、细胞迁移和伤口愈合中的作用一直受到深入研究。基于早期研究的模型表明,Jun 蛋白在增殖和转化中发挥拮抗作用。c-Jun 被认为增强转化,而 JunB 以拮抗方式抑制转化。令人惊讶的是,尽管从动物模型中获得了大量关于 Jun 蛋白在癌症中的作用以及调节它们的致癌途径的信息,但直到最近才证明它们参与了人类癌症。在这里,我们将描述目前关于 Jun 蛋白在人类肿瘤发生中的作用的知识。我们将重点介绍病理实例,证明最初的教条必须重新审查。例如,与 c-Jun 一样,JunB 在淋巴瘤,特别是霍奇金淋巴瘤中似乎发挥致癌作用。此外,与 c-Jun 和 JunB 在转录编码主要细胞周期调节剂(如 CyclinD 或 p16INK4A)的基因中的拮抗活性不同,c-Jun 或 JunB 类似地修饰其他细胞周期调节基因的转录。有趣的是,这些基因中的一些,如编码 CyclinA 或 p19(ARF)的基因,是细胞增殖和存活的正或负调节中的重要参与者。最后,我们还将讨论结果,这些结果表明,迄今为止已知的 c-Jun 的主要激活剂 JNK,作为 c-Jun 水平和活性的负调节剂。这些新发现表明,每个 Jun 蛋白在肿瘤发生以及细胞存活中的作用都应该以依赖于上下文的方式进行检查。

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