Reactive oxygen species as mediators of the transformed phenotype.

Standard

Reactive oxygen species as mediators of the transformed phenotype. / Jürgensmeier, J M; Panse, Jens; Schäfer, R; Bauer, G.

in: INT J CANCER, Jahrgang 70, Nr. 5, 5, 1997, S. 587-589.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Jürgensmeier, JM, Panse, J, Schäfer, R & Bauer, G 1997, 'Reactive oxygen species as mediators of the transformed phenotype.', INT J CANCER, Jg. 70, Nr. 5, 5, S. 587-589. <http://www.ncbi.nlm.nih.gov/pubmed/9052760?dopt=Citation>

APA

Jürgensmeier, J. M., Panse, J., Schäfer, R., & Bauer, G. (1997). Reactive oxygen species as mediators of the transformed phenotype. INT J CANCER, 70(5), 587-589. [5]. http://www.ncbi.nlm.nih.gov/pubmed/9052760?dopt=Citation

Vancouver

Jürgensmeier JM, Panse J, Schäfer R, Bauer G. Reactive oxygen species as mediators of the transformed phenotype. INT J CANCER. 1997;70(5):587-589. 5.

Bibtex

@article{0a2b424d42f4485d8a74bba9dc99c0ec,
title = "Reactive oxygen species as mediators of the transformed phenotype.",
abstract = "Reactive oxygen species (ROS) are known to be involved in different pro- and anticarcinogenic mechanisms. However, their influence on the maintenance of the transformed phenotype has not been studied so far. Here we show that the anchorage-independent growth of transformed murine fibroblasts is inhibited by antioxidants and radical scavengers in a concentration-dependent and reversible manner. These agents also reduce TGF-beta-dependent stimulation of colony formation in soft agar, pointing to their specific interference with TGF-beta-triggered signal chains involved in the maintenance of the transformed state.",
author = "J{\"u}rgensmeier, {J M} and Jens Panse and R Sch{\"a}fer and G Bauer",
year = "1997",
language = "Deutsch",
volume = "70",
pages = "587--589",
journal = "INT J CANCER",
issn = "0020-7136",
publisher = "Wiley-Liss Inc.",
number = "5",

}

RIS

TY - JOUR

T1 - Reactive oxygen species as mediators of the transformed phenotype.

AU - Jürgensmeier, J M

AU - Panse, Jens

AU - Schäfer, R

AU - Bauer, G

PY - 1997

Y1 - 1997

N2 - Reactive oxygen species (ROS) are known to be involved in different pro- and anticarcinogenic mechanisms. However, their influence on the maintenance of the transformed phenotype has not been studied so far. Here we show that the anchorage-independent growth of transformed murine fibroblasts is inhibited by antioxidants and radical scavengers in a concentration-dependent and reversible manner. These agents also reduce TGF-beta-dependent stimulation of colony formation in soft agar, pointing to their specific interference with TGF-beta-triggered signal chains involved in the maintenance of the transformed state.

AB - Reactive oxygen species (ROS) are known to be involved in different pro- and anticarcinogenic mechanisms. However, their influence on the maintenance of the transformed phenotype has not been studied so far. Here we show that the anchorage-independent growth of transformed murine fibroblasts is inhibited by antioxidants and radical scavengers in a concentration-dependent and reversible manner. These agents also reduce TGF-beta-dependent stimulation of colony formation in soft agar, pointing to their specific interference with TGF-beta-triggered signal chains involved in the maintenance of the transformed state.

M3 - SCORING: Zeitschriftenaufsatz

VL - 70

SP - 587

EP - 589

JO - INT J CANCER

JF - INT J CANCER

SN - 0020-7136

IS - 5

M1 - 5

ER -