Chemokine CXCL13 is overexpressed in the tumour tissue and in the peripheral blood of breast cancer patients.

Standard

Chemokine CXCL13 is overexpressed in the tumour tissue and in the peripheral blood of breast cancer patients. / Panse, Jens; Friedrichs, K; Marx, Andreas; Hildebrandt, Y; Luetkens, T; Barrels, K; Horn, C; Stahl, T; Cao, Yanran; Milde-Langosch, Karin; Niendorf, A; Kröger, Nicolaus; Wenzel, S; Leuwer, R; Bokemeyer, Carsten; Hegewisch-Becker, Susanna; Atanackovic, Djordje.

In: BRIT J CANCER, Vol. 99, No. 6, 6, 2008, p. 930-938.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Panse, J, Friedrichs, K, Marx, A, Hildebrandt, Y, Luetkens, T, Barrels, K, Horn, C, Stahl, T, Cao, Y, Milde-Langosch, K, Niendorf, A, Kröger, N, Wenzel, S, Leuwer, R, Bokemeyer, C, Hegewisch-Becker, S & Atanackovic, D 2008, 'Chemokine CXCL13 is overexpressed in the tumour tissue and in the peripheral blood of breast cancer patients.', BRIT J CANCER, vol. 99, no. 6, 6, pp. 930-938. <http://www.ncbi.nlm.nih.gov/pubmed/18781150?dopt=Citation>

APA

Panse, J., Friedrichs, K., Marx, A., Hildebrandt, Y., Luetkens, T., Barrels, K., Horn, C., Stahl, T., Cao, Y., Milde-Langosch, K., Niendorf, A., Kröger, N., Wenzel, S., Leuwer, R., Bokemeyer, C., Hegewisch-Becker, S., & Atanackovic, D. (2008). Chemokine CXCL13 is overexpressed in the tumour tissue and in the peripheral blood of breast cancer patients. BRIT J CANCER, 99(6), 930-938. [6]. http://www.ncbi.nlm.nih.gov/pubmed/18781150?dopt=Citation

Vancouver

Panse J, Friedrichs K, Marx A, Hildebrandt Y, Luetkens T, Barrels K et al. Chemokine CXCL13 is overexpressed in the tumour tissue and in the peripheral blood of breast cancer patients. BRIT J CANCER. 2008;99(6):930-938. 6.

Bibtex

@article{9b1bf716278247a58c709759e07c6120,
title = "Chemokine CXCL13 is overexpressed in the tumour tissue and in the peripheral blood of breast cancer patients.",
abstract = "The abilities of chemokines in orchestrating cellular migration are utilised by different (patho-)biological networks including malignancies. However, except for CXCR4/CXCL12, little is known about the relation between tumour-related chemokine expression and the development and progression of solid tumours like breast cancer. In this study, microarray analyses revealed the overexpression of chemokine CXCL13 in breast cancer specimens. This finding was confirmed by real-time polymerase chain reaction in a larger set of samples (n = 34) and cell lines, and was validated on the protein level performing Western blot, ELISA, and immunohistochemistry. Levels of CXCR5, the receptor for CXCL13, were low in malignant and healthy breast tissues, and surface expression was not detected in vitro. However, we observed a strong (P = 0.0004) correlation between the expressions of CXCL13 and CXCR5 in breast cancer tissues, indicating a biologically relevant role of CXCR5 in vivo. Finally, we detected significantly elevated serum concentrations of CXCL13 in patients with metastatic disease (n = 54) as compared with controls (n = 44) and disease-free patients (n = 48). In conclusion, CXCL13 is overexpressed within breast cancer tissues, and increased serum levels of this cytokine can be found in breast cancer patients with metastatic disease pointing to a role of CXCL13 in the progression of breast cancer, suggesting that CXCL13 might serve as a useful therapeutic target and/or diagnostic marker in this malignancy.",
author = "Jens Panse and K Friedrichs and Andreas Marx and Y Hildebrandt and T Luetkens and K Barrels and C Horn and T Stahl and Yanran Cao and Karin Milde-Langosch and A Niendorf and Nicolaus Kr{\"o}ger and S Wenzel and R Leuwer and Carsten Bokemeyer and Susanna Hegewisch-Becker and Djordje Atanackovic",
year = "2008",
language = "Deutsch",
volume = "99",
pages = "930--938",
journal = "BRIT J CANCER",
issn = "0007-0920",
publisher = "NATURE PUBLISHING GROUP",
number = "6",

}

RIS

TY - JOUR

T1 - Chemokine CXCL13 is overexpressed in the tumour tissue and in the peripheral blood of breast cancer patients.

AU - Panse, Jens

AU - Friedrichs, K

AU - Marx, Andreas

AU - Hildebrandt, Y

AU - Luetkens, T

AU - Barrels, K

AU - Horn, C

AU - Stahl, T

AU - Cao, Yanran

AU - Milde-Langosch, Karin

AU - Niendorf, A

AU - Kröger, Nicolaus

AU - Wenzel, S

AU - Leuwer, R

AU - Bokemeyer, Carsten

AU - Hegewisch-Becker, Susanna

AU - Atanackovic, Djordje

PY - 2008

Y1 - 2008

N2 - The abilities of chemokines in orchestrating cellular migration are utilised by different (patho-)biological networks including malignancies. However, except for CXCR4/CXCL12, little is known about the relation between tumour-related chemokine expression and the development and progression of solid tumours like breast cancer. In this study, microarray analyses revealed the overexpression of chemokine CXCL13 in breast cancer specimens. This finding was confirmed by real-time polymerase chain reaction in a larger set of samples (n = 34) and cell lines, and was validated on the protein level performing Western blot, ELISA, and immunohistochemistry. Levels of CXCR5, the receptor for CXCL13, were low in malignant and healthy breast tissues, and surface expression was not detected in vitro. However, we observed a strong (P = 0.0004) correlation between the expressions of CXCL13 and CXCR5 in breast cancer tissues, indicating a biologically relevant role of CXCR5 in vivo. Finally, we detected significantly elevated serum concentrations of CXCL13 in patients with metastatic disease (n = 54) as compared with controls (n = 44) and disease-free patients (n = 48). In conclusion, CXCL13 is overexpressed within breast cancer tissues, and increased serum levels of this cytokine can be found in breast cancer patients with metastatic disease pointing to a role of CXCL13 in the progression of breast cancer, suggesting that CXCL13 might serve as a useful therapeutic target and/or diagnostic marker in this malignancy.

AB - The abilities of chemokines in orchestrating cellular migration are utilised by different (patho-)biological networks including malignancies. However, except for CXCR4/CXCL12, little is known about the relation between tumour-related chemokine expression and the development and progression of solid tumours like breast cancer. In this study, microarray analyses revealed the overexpression of chemokine CXCL13 in breast cancer specimens. This finding was confirmed by real-time polymerase chain reaction in a larger set of samples (n = 34) and cell lines, and was validated on the protein level performing Western blot, ELISA, and immunohistochemistry. Levels of CXCR5, the receptor for CXCL13, were low in malignant and healthy breast tissues, and surface expression was not detected in vitro. However, we observed a strong (P = 0.0004) correlation between the expressions of CXCL13 and CXCR5 in breast cancer tissues, indicating a biologically relevant role of CXCR5 in vivo. Finally, we detected significantly elevated serum concentrations of CXCL13 in patients with metastatic disease (n = 54) as compared with controls (n = 44) and disease-free patients (n = 48). In conclusion, CXCL13 is overexpressed within breast cancer tissues, and increased serum levels of this cytokine can be found in breast cancer patients with metastatic disease pointing to a role of CXCL13 in the progression of breast cancer, suggesting that CXCL13 might serve as a useful therapeutic target and/or diagnostic marker in this malignancy.

M3 - SCORING: Zeitschriftenaufsatz

VL - 99

SP - 930

EP - 938

JO - BRIT J CANCER

JF - BRIT J CANCER

SN - 0007-0920

IS - 6

M1 - 6

ER -