PD2/PAF1 at the Crossroads of the Cancer Network

被引:31
|
作者
Karmakar, Saswati [1 ]
Dey, Parama [1 ]
Vaz, Arokia P. [1 ]
Bhaumik, Sukesh R. [2 ]
Ponnusamy, Moorthy P. [1 ,3 ,4 ]
Batra, Surinder K. [1 ,3 ,4 ]
机构
[1] Univ Nebraska Med Ctr, Dept Biochem & Mol Biol, 7054 DRC1 985870, Omaha, NE 68198 USA
[2] Southern Illinois Univ, Sch Med, Dept Biochem & Mol Biol, Carbondale, IL 62901 USA
[3] Univ Nebraska Med Ctr, Eppley Inst Res Canc, Omaha, NE USA
[4] Univ Nebraska Med Ctr, Allied Dis & Buffett Canc Ctr, Omaha, NE USA
关键词
RNA-POLYMERASE-II; PAF1; COMPLEX; TRANSCRIPTIONAL ELONGATION; SELF-RENEWAL; HISTONE METHYLATION; FACTOR-1; STEM-CELLS; DIFFERENTIATION; TUMORIGENESIS; RECRUITMENT;
D O I
10.1158/0008-5472.CAN-17-2175
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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. (C) 2018 AACR.
引用
收藏
页码:313 / 319
页数:7
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