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PD2/PAF1 在癌症网络的十字路口。

PD2/PAF1 at the Crossroads of the Cancer Network.

机构信息

Department of Biochemistry and Molecular Biology, University of Nebraska Medical Center, Omaha, Nebraska.

Department of Biochemistry and Molecular Biology, Southern Illinois University School of Medicine, Carbondale, Illinois.

出版信息

Cancer Res. 2018 Jan 15;78(2):313-319. doi: 10.1158/0008-5472.CAN-17-2175. Epub 2018 Jan 8.

Abstract

Pancreatic differentiation 2 (PD2)/RNA polymerase II-associated factor 1 (PAF1) is the core subunit of the human PAF1 complex (PAF1C) that regulates the promoter-proximal pausing of RNA polymerase II as well as transcription elongation and mRNA processing and coordinates events in mRNA stability and quality control. As an integral part of its transcription-regulatory function, PD2/PAF1 plays a role in posttranslational histone covalent modifications as well as regulates expression of critical genes of the cell-cycle machinery. PD2/PAF1 alone, and as a part of PAF1C, provides distinct roles in the maintenance of self-renewal of embryonic stem cells and cancer stem cells, and in lineage differentiation. Thus, PD2/PAF1 malfunction or its altered abundance is likely to affect normal cellular functions, leading to disease states. Indeed, PD2/PAF1 is found to be upregulated in poorly differentiated pancreatic cancer cells and has the capacity for neoplastic transformation when ectopically expressed in mouse fibroblast cells. Likewise, PD2/PAF1 is upregulated in pancreatic and ovarian cancer stem cells. Here, we concisely describe multifaceted roles of PD2/PAF1 associated with oncogenic transformation and implicate PD2/PAF1 as an attractive target for therapeutic development to combat malignancy. .

摘要

胰腺分化 2 (PD2)/RNA 聚合酶 II 相关因子 1 (PAF1) 是人类 PAF1 复合物 (PAF1C) 的核心亚基,它调节 RNA 聚合酶 II 的启动子近端暂停以及转录延伸和 mRNA 加工,并协调 mRNA 稳定性和质量控制中的事件。作为其转录调节功能的一个组成部分,PD2/PAF1 在后翻译组蛋白共价修饰中发挥作用,并调节细胞周期机制的关键基因的表达。PD2/PAF1 单独作为 PAF1C 的一部分,在维持胚胎干细胞和癌症干细胞的自我更新以及谱系分化中发挥独特的作用。因此,PD2/PAF1 功能障碍或其丰度改变可能会影响正常的细胞功能,导致疾病状态。事实上,在分化不良的胰腺癌细胞中发现 PD2/PAF1 上调,并且当其在小鼠成纤维细胞中异位表达时具有致癌转化的能力。同样,PD2/PAF1 在胰腺和卵巢癌细胞干细胞中上调。在这里,我们简要描述了 PD2/PAF1 与致癌转化相关的多方面作用,并暗示 PD2/PAF1 是治疗开发的有吸引力的靶点,以对抗恶性肿瘤。

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