Literature DB >> 3017458

Transformation of established murine fibroblasts with an activated cellular Harvey-ras oncogene or the polyoma virus middle T gene increases cell permissiveness to parvovirus minute-virus-of-mice.

S Mousset, J Cornelis, N Spruyt, J Rommelaere.   

Abstract

Transformation of permanent rodent fibroblast cells by the polyoma virus middle T gene or the activated human Harvey-ras oncogene results in increased cellular permissiveness to the autonomous parvovirus minute-virus-of-mice. Parvoviral DNA amplification is restricted in the untransformed parental cell lines. Analysis of various parameters of the parvoviral life cycle shows that this block is partially overcome in the transformed lines.

Entities:  

Mesh：

Substances：

Year:  1986        PMID： 3017458     DOI： 10.1016/s0300-9084(86)81058-6

Source DB:  PubMed          Journal:  Biochimie        ISSN： 0300-9084            Impact factor:   4.079


  11 in total

1.  Selective killing of transformed rat cells by minute virus of mice does not require infectious virus production.

Authors:  E Guetta; M Mincberg; S Mousset; C Bertinchamps; J Rommelaere; J Tal
Journal:  J Virol       Date:  1990-01       Impact factor: 5.103

2.  Partial reversion of conditional transformation correlates with a decrease in the sensitivity of rat cells to killing by the parvovirus minute virus of mice but not in their capacity for virus production: effect of a temperature-sensitive v-src oncogene.

Authors:  N Salome; B van Hille; M Geuskens; J Rommelaere
Journal:  J Virol       Date:  1989-11       Impact factor: 5.103

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

Authors:  J J Cornelis; N Spruyt; P Spegelaere; E Guetta; T Darawshi; S F Cotmore; J Tal; J Rommelaere
Journal:  J Virol       Date:  1988-09       Impact factor: 5.103

4.  The cytotoxicity of the autonomous parvovirus minute virus of mice nonstructural proteins in FR3T3 rat cells depends on oncogene expression.

Authors:  S Mousset; Y Ouadrhiri; P Caillet-Fauquet; J Rommelaere
Journal:  J Virol       Date:  1994-10       Impact factor: 5.103

5.  Transformation-dependent expression of interleukin genes delivered by a recombinant parvovirus.

Authors:  S J Russell; A Brandenburger; C L Flemming; M K Collins; J Rommelaere
Journal:  J Virol       Date:  1992-05       Impact factor: 5.103

6.  Induction of an embryonic mouse innate immune response following inoculation in utero with minute virus of mice.

Authors:  Irina Rostovsky; Claytus Davis
Journal:  J Virol       Date:  2014-12-03       Impact factor: 5.103

7.  Neoplastic transformation-associated stimulation of the in vitro resolution of concatemer junction fragments from minute virus of mice DNA.

Authors:  G Kuntz-Simon; T Bashir; J Rommelaere; K Willwand
Journal:  J Virol       Date:  1999-03       Impact factor: 5.103

8.  Parvoviruses are inefficient in inducing interferon-beta, tumor necrosis factor-alpha, or interleukin-6 in mammalian cells.

Authors:  J R Schlehofer; M Rentrop; D N Männel
Journal:  Med Microbiol Immunol       Date:  1992       Impact factor: 3.402

9.  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.

Authors:  J J Cornelis; P Becquart; N Duponchel; N Salomé; B L Avalosse; M Namba; J Rommelaere
Journal:  J Virol       Date:  1988-05       Impact factor: 5.103

10.  Parvovirus replication in normal and transformed human cells correlates with the nuclear translocation of the early protein NS1.

Authors:  S L Rhode; P R Paradiso
Journal:  J Virol       Date:  1989-01       Impact factor: 5.103
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.