Artificial microRNAs against the viral E6 protein provoke apoptosis in HPV positive cancer cells

被引:19
作者
Bonetta, Anaelle Charlotte [1 ,2 ]
Mailly, Laurent [3 ]
Robinet, Eric [3 ]
Trave, Gilles [1 ,2 ]
Masson, Murielle [1 ,2 ]
Deryckere, Francois [1 ,2 ]
机构
[1] IREBS, UMR7242, F-67412 Illkirch Graffenstaden, France
[2] Univ Strasbourg, CNRS, Strasbourg, France
[3] INSERM, U1110, Inst Rech Malad Virales & Hepat, Strasbourg, France
关键词
Cancer therapy; Gene therapy; Adenovirus; Cervical cancer; RNA interference; RNA INTERFERENCE; IN-VIVO; SIRNA; PAPILLOMAVIRUSES; CARCINOGENESIS; DEATH; E7;
D O I
10.1016/j.bbrc.2015.07.144
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
High-risk human papillomavirus (HPV) types 16 and 18 are associated with more than 70% of cervical cancer cases. The oncoprotein E6 is multifunctional and has numerous cellular partners. The best-known activity of E6 is the polyubiquination of the pro-apoptotic tumor suppressor p53, targeting it for degradation by the 26S proteasome. Loss of p53 triggers genomic instability and favors cancer development. Here, we generated recombinant adenovirus (Ad) vectors expressing artificial microRNAs directed against HPV16 E6 (Ad16_1) or HPV18 E6 (Ad18_2). E6-knockdown was observed in HeLa after treatment with Ad18_2 and in SiHa with Ad16_1. Western-blot experiments found an increase in p53 levels after treatment in both cell lines. Cell death was observed in both cell lines after knockdown of E6. Further analysis such as cleavage of caspases (3 and 7) as well as of PARP1 indicated that treated HeLa and SiHa cells underwent apoptosis. The growth of HeLa-derived tumors developed in nude mice was significantly reduced after intra-tumoral injection of Ad18_2. Therefore, vectorisation of artificial miRNA against E6 oncoprotein by means of recombinant adenoviruses might represent a valuable therapeutic approach for treating HPV-positive cancers. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:658 / 664
页数:7
相关论文
共 20 条
  • [1] MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004)
    Bartel, David P.
    [J]. CELL, 2007, 131 (04) : 11 - 29
  • [2] Association of oncolytic adenoviruses with chemotherapies: An overview and future directions
    Bressy, Christian
    Benihoud, Karim
    [J]. BIOCHEMICAL PHARMACOLOGY, 2014, 90 (02) : 97 - 106
  • [3] siRNA targeting of the viral E6 oncogene efficiently kills human papillomavirus-positive cancer cells
    Butz, K
    Ristriani, T
    Hengstermann, A
    Denk, C
    Scheffner, M
    Hoppe-Seyler, F
    [J]. ONCOGENE, 2003, 22 (38) : 5938 - 5945
  • [4] Down-regulation of HPV18 E6, E7, or VEGF expression attenuates malignant biological behavior of human cervical cancer cells
    Chen, Li
    Wu, Yuan-Yuan
    Liu, Peigen
    Wang, Jianli
    Wang, Guilan
    Qin, Jin
    Zhou, Jiaming
    Zhu, Jianwei
    [J]. MEDICAL ONCOLOGY, 2011, 28 : S528 - S539
  • [5] Dissecting p53-dependent apoptosis
    Chipuk, J. E.
    Green, D. R.
    [J]. CELL DEATH AND DIFFERENTIATION, 2006, 13 (06) : 994 - 1002
  • [6] Adenovirus: The First Effective In Vivo Gene Delivery Vector
    Crystal, Ronald G.
    [J]. HUMAN GENE THERAPY, 2014, 25 (01) : 3 - 11
  • [7] Classification of papillomaviruses
    de Villiers, EM
    Fauquet, C
    Broker, TR
    Bernard, HU
    zur Hausen, H
    [J]. VIROLOGY, 2004, 324 (01) : 17 - 27
  • [8] The regulation of cell proliferation by the papillomavirus early proteins
    Hamid, N. Abdul
    Brown, C.
    Gaston, K.
    [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2009, 66 (10) : 1700 - 1717
  • [9] Gene silencing of HPV16 E6/E7 induced by promoter-targeting siRNA in SiHa cells
    Hong, D.
    Lu, W.
    Ye, F.
    Hu, Y.
    Xie, X.
    [J]. BRITISH JOURNAL OF CANCER, 2009, 101 (10) : 1798 - 1804
  • [10] Intracellular scFvs against the viral E6 oncoprotein provoke apoptosis in human papillomavirus-positive cancer cells
    Lagrange, Magali
    Boulade-Ladame, Charlotte
    Mailly, Laurent
    Weiss, Etienne
    Orfanoudakis, Georges
    Deryckere, Francois
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 361 (02) : 487 - 492