Literature DB >> 2867825

gamma-Glutamyltranspeptidase and the ras-induced transformation of a rat liver cell line.

S Sinha, C J Marshall, G E Neal.   

Abstract

The effects of activated ras genes on a continuously dividing, nontransformed, rat liver-derived epithelial cell line have been studied. Genes have been introduced into cells in conjunction with a selectable drug (G418) resistance marker. Controls were obtained by transfecting with the drug resistance gene alone. Transformed, drug-resistance colonies were obtained on transfecting with ras plus resistance marker genes. They had an altered morphology, a tendency to pile up in culture, and showed anchorage-independent growth. They also were tumorigenic in nude mice with a short latent period. None of these properties was exhibited by nontransformed, drug-resistant colonies. Transformed clones were positive on histochemical staining for the enzyme gamma-glutamyltranspeptidase. A heterogeneity of gamma-glutamyltranspeptidase activity between cells of the same transformed clone was revealed by both histochemical and cytofluorographic assays. Nontransformed clones failed to stain histochemically for the enzyme. The fluorimetric determination of the specific activity of the enzyme showed consistently higher levels in transformed cells as compared to nontransformed, drug-resistant controls. The possible relationship between cell transformation and elevated levels of gamma-glutamyltranspeptidase is discussed.

Entities:  

Mesh:

Substances:

Year:  1986        PMID: 2867825

Source DB:  PubMed          Journal:  Cancer Res        ISSN: 0008-5472            Impact factor:   12.701


  11 in total

1.  Extensive intra-tumor heterogeneity in primary human glial tumors as a result of locus non-specific genomic alterations.

Authors:  A Misra; P Chattopadhyay; A K Dinda; C Sarkar; A K Mahapatra; S E Hasnain; S Sinha
Journal:  J Neurooncol       Date:  2000-05       Impact factor: 4.130

2.  Sensitivity of the cell cycle to TGF beta 1 does not correlate with transformation of a rat liver epithelial cell line.

Authors:  R Davies; R F Legg; G E Neal
Journal:  Cell Biol Toxicol       Date:  1990-10       Impact factor: 6.691

3.  Characterization of liver epithelial cells transfected with myc and/or ras oncogenes.

Authors:  S C Strom; J B Faust; E Cappelluti; R B Harris; N D Lalwani
Journal:  Dig Dis Sci       Date:  1991-05       Impact factor: 3.199

4.  4-Hydroxynonenal increases gamma-glutamyl transpeptidase gene expression through mitogen-activated protein kinase pathways.

Authors:  Hongqiao Zhang; Dale A Dickinson; Rui-Ming Liu; Henry Jay Forman
Journal:  Free Radic Biol Med       Date:  2005-02-15       Impact factor: 7.376

Review 5.  Enzymes of glutathione metabolism as biochemical markers during hepatocarcinogenesis.

Authors:  S Hendrich; H C Pitot
Journal:  Cancer Metastasis Rev       Date:  1987       Impact factor: 9.264

6.  Activation of ras oncogene in aflatoxin-induced rat liver carcinogenesis.

Authors:  S Sinha; C Webber; C J Marshall; M A Knowles; A Proctor; N C Barrass; G E Neal
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

7.  MTrasT24, a metallothionein-ras fusion gene, modulates expression in cultured rat liver cells of two genes associated with in vivo liver cancer.

Authors:  Y C Li; T Seyama; A K Godwin; T S Winokur; R M Lebovitz; M W Lieberman
Journal:  Proc Natl Acad Sci U S A       Date:  1988-01       Impact factor: 11.205

Review 8.  gamma-Glutamyl transpeptidase. What does the organization and expression of a multipromoter gene tell us about its functions?

Authors:  M W Lieberman; R Barrios; B Z Carter; G M Habib; R M Lebovitz; S Rajagopalan; A R Sepulveda; Z Z Shi; D F Wan
Journal:  Am J Pathol       Date:  1995-11       Impact factor: 4.307

9.  The expression of c-myc related to the proliferation and transformation of rat liver-derived epithelial cells.

Authors:  S Sinha; G E Neal; R F Legg; J V Watson; C Pearson
Journal:  Br J Cancer       Date:  1989-05       Impact factor: 7.640

10.  A system for transformation of rat liver cells in vitro by acute treatment with aflatoxin.

Authors:  S Sinha; L J Hockin; G E Neal
Journal:  Br J Cancer       Date:  1987-06       Impact factor: 7.640

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.