TY - JOUR
T1 - Tissue kallikrein-related peptidase 4 (KLK4), a novel biomarker in triple-negative breast cancer
AU - Yang, Feng
AU - Aubele, Michaela
AU - Walch, Axel
AU - Gross, Eva
AU - Napieralski, Rudolf
AU - Zhao, Shuo
AU - Ahmed, Nancy
AU - Kiechle, Marion
AU - Reuning, Ute
AU - Dorn, Julia
AU - Sweep, Fred
AU - Magdolen, Viktor
AU - Schmitt, Manfred
N1 - Publisher Copyright:
© 2017 Walter de Gruyter GmbH, Berlin/Boston 2017.
PY - 2017/9/26
Y1 - 2017/9/26
N2 - Triple-negative breast cancer (TNBC), lacking the steroid hormone receptors ER and PR and the oncoprotein HER2, is characterized by its aggressive pattern and insensitivity to endocrine and HER2-directed therapy. Human kallikrein-related peptidases KLK1-15 provide a rich source of serine protease-type biomarkers associated with tumor growth and cancer progression for a variety of malignant diseases. In this study, recombinant KLK4 protein was generated and affinity-purified KLK4-directed polyclonal antibody pAb587 established to allow localization of KLK4 protein expression in tumor cell lines and archived formalin-fixed, paraffin-embedded TNBC tumor tissue specimens. For this, KLK4 protein expression was assessed by immunohistochemistry in primary tumor tissue sections (tissue microarrays) of 188 TNBC patients, mainly treated with anthracycline- or CMF-based polychemotherapy. KLK4 protein is localized in the cytoplasm of tumor and stroma cells. In this patient cohort, elevated stroma cell KLK4 expression, but not tumor cell KLK4 expression, is predictive for poor disease-free survival by univariate analysis (hazard ratio: 2.26, p=0.001) and multivariable analysis (hazard ratio: 2.12, p<0.01). Likewise, univariate analysis revealed a trend for statistical significance of elevated KLK4 stroma cell expression for overall survival of TNBC patients as well.
AB - Triple-negative breast cancer (TNBC), lacking the steroid hormone receptors ER and PR and the oncoprotein HER2, is characterized by its aggressive pattern and insensitivity to endocrine and HER2-directed therapy. Human kallikrein-related peptidases KLK1-15 provide a rich source of serine protease-type biomarkers associated with tumor growth and cancer progression for a variety of malignant diseases. In this study, recombinant KLK4 protein was generated and affinity-purified KLK4-directed polyclonal antibody pAb587 established to allow localization of KLK4 protein expression in tumor cell lines and archived formalin-fixed, paraffin-embedded TNBC tumor tissue specimens. For this, KLK4 protein expression was assessed by immunohistochemistry in primary tumor tissue sections (tissue microarrays) of 188 TNBC patients, mainly treated with anthracycline- or CMF-based polychemotherapy. KLK4 protein is localized in the cytoplasm of tumor and stroma cells. In this patient cohort, elevated stroma cell KLK4 expression, but not tumor cell KLK4 expression, is predictive for poor disease-free survival by univariate analysis (hazard ratio: 2.26, p=0.001) and multivariable analysis (hazard ratio: 2.12, p<0.01). Likewise, univariate analysis revealed a trend for statistical significance of elevated KLK4 stroma cell expression for overall survival of TNBC patients as well.
KW - KLK4
KW - biomarker
KW - immunohistochemistry
KW - kallikrein-related peptidase
KW - predictive
KW - triple-negative breast cancer
UR - http://www.scopus.com/inward/record.url?scp=85029327048&partnerID=8YFLogxK
U2 - 10.1515/hsz-2017-0122
DO - 10.1515/hsz-2017-0122
M3 - Article
C2 - 28755528
AN - SCOPUS:85029327048
SN - 1431-6730
VL - 398
SP - 1151
EP - 1164
JO - Biological Chemistry
JF - Biological Chemistry
IS - 10
ER -