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AP-1/c-Jun 转录因子:在恶性黑素瘤中的调控和功能。

AP-1/c-Jun transcription factors: regulation and function in malignant melanoma.

机构信息

Institute of Pathology, Molecular Pathology, University of Regensburg, Germany.

Institute of Pathology, Molecular Pathology, University of Regensburg, Germany.

出版信息

Eur J Cell Biol. 2014 Jan-Feb;93(1-2):76-81. doi: 10.1016/j.ejcb.2013.10.003. Epub 2013 Oct 26.

Abstract

Malignant melanoma is an aggressive form of skin cancer with an increasing incidence worldwide. One way to address the pathology of the disease is through molecular research. In addition to the analysis of melanoma-relevant signaling pathways, the investigation of important transcription factors is a fundamental objective. The AP-1 transcription factor family is known to play an important role in melanoma progression and development. The AP-1 family member c-Jun is highly expressed and active in melanoma cells, and the mechanisms and signaling pathways regulating c-Jun protein are diverse. In addition to the common regulation and activation of c-Jun by mitogen-activated protein kinases (MAPKs), there are several other signaling pathways and interactions leading to c-Jun protein expression and thus AP-1 activation. In malignant melanoma, and many other cancer types, c-Jun has mainly oncogenic functions; however, other AP-1 proteins also have anti-oncogenic roles. Interestingly, several studies have revealed that a strong AP-1 activity in melanoma mainly depends on c-Jun. Recently, it has also been shown that the c-Jun protein is regulated and activated by several other mechanisms, including miRNAs and the cytoskeleton. In summary, there are a variety of mechanisms underlying the induction of c-Jun protein expression and activity leading to tumor progression and development, and this diverse regulatory machinery is due to the heterogeneity of different tumor types, particularly in malignant melanoma.

摘要

恶性黑色素瘤是一种具有侵袭性的皮肤癌,其发病率在全球范围内呈上升趋势。解决该疾病病理学的一种方法是通过分子研究。除了分析与黑色素瘤相关的信号通路外,研究重要的转录因子也是一个基本目标。AP-1 转录因子家族被认为在黑色素瘤的进展和发展中起着重要作用。AP-1 家族成员 c-Jun 在黑色素瘤细胞中高度表达和活跃,调节 c-Jun 蛋白的机制和信号通路多种多样。除了丝裂原活化蛋白激酶 (MAPKs) 对 c-Jun 的常见调节和激活外,还有其他几种信号通路和相互作用导致 c-Jun 蛋白表达和因此 AP-1 激活。在恶性黑色素瘤和许多其他癌症类型中,c-Jun 主要具有致癌功能;然而,其他 AP-1 蛋白也具有抗肿瘤作用。有趣的是,几项研究表明,黑色素瘤中强大的 AP-1 活性主要依赖于 c-Jun。最近,还表明 c-Jun 蛋白受多种其他机制的调节和激活,包括 microRNA 和细胞骨架。总之,有多种机制诱导 c-Jun 蛋白表达和活性,导致肿瘤的进展和发展,这种多样化的调控机制是由于不同肿瘤类型的异质性,特别是在恶性黑色素瘤中。

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