C-Fos expression is a molecular predictor of progression and survival in epithelial ovarian carcinoma.

Standard

C-Fos expression is a molecular predictor of progression and survival in epithelial ovarian carcinoma. / Mahner, Sven; Baasch, C; Schwarz, J; Hein, Sybill; Wölber, L; Jänicke, Fritz; Milde-Langosch, Karin.

in: BRIT J CANCER, Jahrgang 99, Nr. 8, 8, 2008, S. 1269-1275.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Mahner, S, Baasch, C, Schwarz, J, Hein, S, Wölber, L, Jänicke, F & Milde-Langosch, K 2008, 'C-Fos expression is a molecular predictor of progression and survival in epithelial ovarian carcinoma.', BRIT J CANCER, Jg. 99, Nr. 8, 8, S. 1269-1275. <http://www.ncbi.nlm.nih.gov/pubmed/18854825?dopt=Citation>

APA

Mahner, S., Baasch, C., Schwarz, J., Hein, S., Wölber, L., Jänicke, F., & Milde-Langosch, K. (2008). C-Fos expression is a molecular predictor of progression and survival in epithelial ovarian carcinoma. BRIT J CANCER, 99(8), 1269-1275. [8]. http://www.ncbi.nlm.nih.gov/pubmed/18854825?dopt=Citation

Vancouver

Mahner S, Baasch C, Schwarz J, Hein S, Wölber L, Jänicke F et al. C-Fos expression is a molecular predictor of progression and survival in epithelial ovarian carcinoma. BRIT J CANCER. 2008;99(8):1269-1275. 8.

Bibtex

@article{2b14cb32fc524f1b9ae9877ff01e23d2,
title = "C-Fos expression is a molecular predictor of progression and survival in epithelial ovarian carcinoma.",
abstract = "Members of the Fos protein family dimerise with Jun proteins to form the AP-1 transcription factor complex. They have a central function in proliferation and differentiation of normal tissue as well as in oncogenic transformation and tumour progression. We analysed the expression of c-Fos, FosB, Fra-1 and Fra-2 to investigate the function of Fos transcription factors in ovarian cancer. A total of 101 patients were included in the study. Expression of Fos proteins was determined by western blot analysis, quantified by densitometry and verified by immunohistochemistry. Reduced c-Fos expression was independently associated with unfavourable progression-free survival (20.6, 31.6 and 51.2 months for patients with low, moderate and high c-Fos expression; P=0.003) as well as overall survival (23.8, 46.0 and 55.5 months for low, moderate and high c-Fos levels; P=0.003). No correlations were observed for FosB, Fra-1 and Fra-2. We conclude that loss of c-Fos expression is associated with tumour progression in ovarian carcinoma and that c-Fos may be a prognostic factor. These results are in contrast to the classic concept of c-Fos as an oncogene, but are supported by the recently discovered tumour-suppressing and proapoptotic function of c-Fos in various cancer types.",
author = "Sven Mahner and C Baasch and J Schwarz and Sybill Hein and L W{\"o}lber and Fritz J{\"a}nicke and Karin Milde-Langosch",
year = "2008",
language = "Deutsch",
volume = "99",
pages = "1269--1275",
journal = "BRIT J CANCER",
issn = "0007-0920",
publisher = "NATURE PUBLISHING GROUP",
number = "8",

}

RIS

TY - JOUR

T1 - C-Fos expression is a molecular predictor of progression and survival in epithelial ovarian carcinoma.

AU - Mahner, Sven

AU - Baasch, C

AU - Schwarz, J

AU - Hein, Sybill

AU - Wölber, L

AU - Jänicke, Fritz

AU - Milde-Langosch, Karin

PY - 2008

Y1 - 2008

N2 - Members of the Fos protein family dimerise with Jun proteins to form the AP-1 transcription factor complex. They have a central function in proliferation and differentiation of normal tissue as well as in oncogenic transformation and tumour progression. We analysed the expression of c-Fos, FosB, Fra-1 and Fra-2 to investigate the function of Fos transcription factors in ovarian cancer. A total of 101 patients were included in the study. Expression of Fos proteins was determined by western blot analysis, quantified by densitometry and verified by immunohistochemistry. Reduced c-Fos expression was independently associated with unfavourable progression-free survival (20.6, 31.6 and 51.2 months for patients with low, moderate and high c-Fos expression; P=0.003) as well as overall survival (23.8, 46.0 and 55.5 months for low, moderate and high c-Fos levels; P=0.003). No correlations were observed for FosB, Fra-1 and Fra-2. We conclude that loss of c-Fos expression is associated with tumour progression in ovarian carcinoma and that c-Fos may be a prognostic factor. These results are in contrast to the classic concept of c-Fos as an oncogene, but are supported by the recently discovered tumour-suppressing and proapoptotic function of c-Fos in various cancer types.

AB - Members of the Fos protein family dimerise with Jun proteins to form the AP-1 transcription factor complex. They have a central function in proliferation and differentiation of normal tissue as well as in oncogenic transformation and tumour progression. We analysed the expression of c-Fos, FosB, Fra-1 and Fra-2 to investigate the function of Fos transcription factors in ovarian cancer. A total of 101 patients were included in the study. Expression of Fos proteins was determined by western blot analysis, quantified by densitometry and verified by immunohistochemistry. Reduced c-Fos expression was independently associated with unfavourable progression-free survival (20.6, 31.6 and 51.2 months for patients with low, moderate and high c-Fos expression; P=0.003) as well as overall survival (23.8, 46.0 and 55.5 months for low, moderate and high c-Fos levels; P=0.003). No correlations were observed for FosB, Fra-1 and Fra-2. We conclude that loss of c-Fos expression is associated with tumour progression in ovarian carcinoma and that c-Fos may be a prognostic factor. These results are in contrast to the classic concept of c-Fos as an oncogene, but are supported by the recently discovered tumour-suppressing and proapoptotic function of c-Fos in various cancer types.

M3 - SCORING: Zeitschriftenaufsatz

VL - 99

SP - 1269

EP - 1275

JO - BRIT J CANCER

JF - BRIT J CANCER

SN - 0007-0920

IS - 8

M1 - 8

ER -