A review
The tumor suppressive properties of adeno-associated viruses

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References (134)

  • P.J. Dyson et al.

    Expression of c-myb in embryonal carcinoma cells and embryonal stem cells

    Differentiation

    (1989)
  • B. Georg-Fries et al.

    Analysis of proteins, helper dependence, and seroepidemiology of a new human parvovirus

    Virology

    (1984)
  • A. Grover et al.

    Roles of extracellular matrix components in differentiating teratocarcinoma cells

    J. Biol. Chem.

    (1985)
  • H. Handa et al.

    Establishment and characterization of KB cell lines latently infected with adeno-associated virus type 1

    Virology

    (1977)
  • R. Heilbronn et al.

    Selective killing of carcinogen-treated SV40-transformed Chinese hamster cells by a defective parvovirus

    Virology

    (1984)
  • P.L. Hermonat

    The adeno-associated virus Rep 78 gene inhibits cellular transformation induced by bovine papillomavirus

    Virology

    (1989)
  • S.N. Khleif et al.

    Inhibition of cellular transformation by the adeno-associated virus rep gene

    Virology

    (1991)
  • R.M. Kotin et al.

    Mapping and direct visualization of a region-specific viral DNA integration site on chromosome 19q13-qter

    Genomics

    (1991)
  • H.D. Mayor et al.

    Antibodies to adeno-associated satellite virus and herpes simplex in sera from cancer patients and normal adults

    Am. J. Obstet. Gynecol.

    (1976)
  • R.A. McPherson et al.

    Human cytomegalovirus completely helps adeno-associated virus replication

    Virology

    (1985)
  • E. Mendelson et al.

    Effect of a viral rep gene on transformation of cells by an adeno-associated virus vector

    Virology

    (1988)
  • L. Mishra et al.

    Adeno-associated virus DNA replication is induced by genes that are essential for HSV-1 DNA synthesis

    Virology

    (1990)
  • R. Moll et al.

    Classification, expression and possible mechanism of patterns of expression of specific cytokeratins in normal epithelial tumors and cultured cells

    Cell

    (1982)
  • J.M. Ostrove et al.

    Adenovirus early region 1b gene function required for rescue of latent adeno-associated virus

    Virology

    (1980)
  • J.M. Ostrove et al.

    Inhibition of adenovirus-transformed cell oncogenicity by adeno-associated virus

    Virology

    (1981)
  • J. Rommelaere et al.

    Antineoplastic activity of parvoviruses

    J. Virol. Methods

    (1991)
  • R.J. Salo et al.

    Adenovirus-associated virus polypeptides synthesized in cells coinfected with either adenovirus or herpesvirus

    Virology

    (1979)
  • J.R. Schlehofer et al.

    Infection with adeno-associated virus type 5 inhibits mutagenicity of herpes simplex virus type 1 or 4-nitroquinoline-1-oxide

    Mutation Res.

    (1990)
  • J.R. Schlehofer et al.

    Induction of mutations within the host cell genome by partially inactivated herpes simplex virus type 1

    Virology

    (1982)
  • J.R. Schlehofer et al.

    Vaccinia virus, herpes simplex virus, and carcinogens induce DNA amplification of a human cell line and support replication of a helpervirus dependent parvovirus

    Virology

    (1986)
  • R.W. Atchison et al.

    Adenovirus-associated defective virus particles

    Science

    (1965)
  • U. Bantel-Schaal

    Adeno-associated parvoviruses inhibit growth of cells derived from malignant human tumors

    Int. J. Cancer

    (1990)
  • U. Bantel-Schaal et al.

    Influence of adeno-associated virus on adherence and growth properties of normal cells

    J. Virol.

    (1992)
  • V.V. Bergs

    Rat virus-mediated suppression of leukemia induction by Moloney virus in rats

    Cancer Res.

    (1969)
  • K.I. Berns

    The Parvoviruses

    (1984)
  • K.I. Berns

    Parvovirus replication

    Microbiol. Rev.

    (1990)
  • K.I. Berns

    Parvoviridae and their replication

  • K.I. Berns et al.

    Separation of two types of adeno-associated virus particles containing complementary polynucleotide chains

    J. Virol.

    (1972)
  • K.I. Berns et al.

    Parvovirus gene regulation

    J. Gen. Virol.

    (1987)
  • K.I. Berns et al.

    Evidence for a single-stranded adeno-associated virus genome: isolation and separation of complementary single strands

    J. Virol.

    (1970)
  • N.R. Blacklow et al.

    Interaction of adeno-associated viruses with cells transformed by herpes simplex virus

  • P. Brulet et al.

    Monoclonal antibodies against trophectoderm-specific markers during mouse blastocyst formation

  • R.M. Buller et al.

    Herpes simplex virus types 1 and 2 completely help adenovirus-associated virus replication

    J. Virol.

    (1981)
  • B.C. Casto et al.

    Inhibition of adenovirus transformation in vitro by AAV-1

  • Y.Q. Chen et al.

    Selective killing of simian virus 40-transformed human fibroblasts by parvovirus H-1

    Cancer Res.

    (1986)
  • Y.Q. Chen et al.

    Sensitization of human keratinocytes to killing by parvovirus H-1 takes place during their malignant transformation but does not require them to be tumorigenic

    Carcinogenesis

    (1989)
  • A.K. Cheung et al.

    Integration of the adeno-associated virus genome into cellular DNA in latently infected human Detroit 6 cells

    J. Virol.

    (1980)
  • S.J. Collins et al.

    Terminal differentiation of human promyelocytic cells induced by dimethyl sulfoxide and other polar compounds

  • J.J. Cornelis et al.

    Transformation of human fibroblasts by ionizing radiation, a chemical carcinogen, or simian virus 40 correlates with an increase in susceptibility to the autonomous parvoviruses H-1 virus and minute virus of mice

    J. Virol.

    (1988)
  • J.J. Cornelis et al.

    Sensitization of transformed rat fibroblasts to killing by parvovirus minute virus of mice correlates with an increase in viral gene expression

    J. Virol.

    (1988)
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    • Analysis of hepatic and retinal cell microRNAome during AAV infection reveals their diverse impact on viral transduction and cellular physiology

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      The results strongly suggests AAV infection cause host-specific microRNA mediated cell cycle alteration. Multiple reports have demonstrated that AAV suppresses the cellular proliferation in tumorigenic cells and induced tumor models (Bantelschaal, 1990; Schlehofer, 1994). The suppressive properties were attributed to the interference of AAV with cell cycle functions (Winocour et al., 1988).

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      Although AAV requires the presence of a helper virus for a fully permissive infection, AAV inhibits Ad replication and gene expression during coinfection (Casto et al., 1967a; Casto et al., 1967b; Jing et al., 2001; Timpe et al., 2006). AAV also acts as a tumor suppressor, restricts Ad-induced cellular proliferation (Khleif et al., 1991; Ostrove et al., 1981), and sensitizes cells to chemotherapeutic agents (Schlehofer, 1994). The AAV genome contains two open reading frames, rep and cap, which encode the nonstructural replication proteins (Rep) and structural capsid proteins (Cap) respectively.

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