miR-24 and miR-205 expression is dependent on HPV onco-protein expression in keratinocytes

被引:24
作者
McKenna, Declan J. [1 ,2 ]
Patel, Daksha [2 ]
McCance, Dennis J. [2 ]
机构
[1] Univ Ulster, Biomed Sci Res Inst, Coleraine BT52 1SA, Co Derry, North Ireland
[2] Queens Univ Belfast, Sch Med Dent & Biomed Sci, Ctr Canc Res & Cell Biol, Belfast BT9 7BL, Antrim, North Ireland
基金
英国医学研究理事会;
关键词
microRNA; miR-24; miR-205; HPV; Keratinocytes; Differentiation; TUMOR-SUPPRESSOR; MICRORNAS; CANCER; DIFFERENTIATION; MIGRATION; CELLS; P53; MORPHOGENESIS; SHIP2; E6;
D O I
10.1016/j.virol.2013.10.014
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A screen of microRNA (miRNA) expression following differentiation in human foreskin keratinocytes (HFKs) identified changes in several miRNAs, including miR-24 and miR-205. We investigated how expression of Human Papilloma Virus Type-16 (HPV16) onco-proteins E6 and E7 affected expression of miR-24 and miR-205 during proliferation and differentiation of HFKs. We show that the induction of both miR-24 and miR-205 observed during differentiation of HFKs is lost in HFKs expressing E6 and E7. We demonstrate that the effect on miR-205 is due to E7 activity, as miR-205 expression is dependent on pRb expression. Finally, we provide evidence that miR-24 effects in the cell may be due to targeting of cyclin dependent kinase inhibitor p27. In summary, these results indicate that expression of both miR-24 and miR-205 are impacted by E6 and/or E7 expression, which may be one mechanism by which HPV onco-proteins can disrupt the balance between proliferation and differentiation in keratinocytes. (C) 2013 The Authors. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:210 / 216
页数:7
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