TY - JOUR
T1 - Stromal cell-associated expression of kallikrein-related peptidase 6 (KLK6) indicates poor prognosis of ovarian cancer patients
AU - Seiz, Lina
AU - Dorn, Julia
AU - Kotzsch, Matthias
AU - Walch, Axel
AU - Grebenchtchikov, Nicolai I.
AU - Gkazepis, Apostolos
AU - Schmalfeldt, Barbara
AU - Kiechle, Marion
AU - Bayani, Jane
AU - Diamandis, Eleftherios P.
AU - Langer, Rupert
AU - Sweep, Fred C.G.J.
AU - Schmitt, Manfred
AU - Magdolen, Viktor
N1 - Funding Information:
This study was supported in part by grants from the Kommission Klinische Forschung der TU M ü nchen and from the German Federal Ministry of Education and Research, Leading-Edge Cluster m4. The excellent technical assistance of Sabine Creutzburg and Daniela Hellmann is gratefully acknowledged. We especially thank Karin Mengele and J ü rgen Schlegel for helpful discussions and provision of brain protein extracts.
PY - 2012/4
Y1 - 2012/4
N2 - Several members of the human kallikrein-related peptidase family, including KLK6, are up-regulated in ovarian cancer. High KLK6 mRNA or protein expression, measured by quantitative polymerase chain reaction and enzyme-linked immunoassay, respectively, was previously found to be associated with a shortened overall and progression-free survival (OS and PFS, respectively). In the present study, we aimed at analyzing KLK6 protein expression in ovarian cancer tissue by immunohistochemistry. Using a newly developed monospecific polyclonal antibody, KLK6 immunoexpression was initially evaluated in normal tissues. We observed strong staining in the brain and moderate staining in the kidney, liver, and ovary, whereas the pancreas and the skeletal muscle were unreactive, which is in line with previously published results. Next, both tumor cell- and stromal cell-associated KLK6 immunoexpression were analyzed in tumor tissue specimens of 118 ovarian cancer patients. In multivariate Cox regression analysis, only stromal cell-associated expression, besides the established clinical parameters FIGO stage and residual tumor mass, was found to be statistically significant for OS and PFS [high vs. low KLK6 expression; hazard ratio (HR), 1.92; p=0.017; HR, 1.80; p=0.042, respectively]. These results indicate that KLK6 expressed by stromal cells may considerably contribute to the aggressiveness of ovarian cancer.
AB - Several members of the human kallikrein-related peptidase family, including KLK6, are up-regulated in ovarian cancer. High KLK6 mRNA or protein expression, measured by quantitative polymerase chain reaction and enzyme-linked immunoassay, respectively, was previously found to be associated with a shortened overall and progression-free survival (OS and PFS, respectively). In the present study, we aimed at analyzing KLK6 protein expression in ovarian cancer tissue by immunohistochemistry. Using a newly developed monospecific polyclonal antibody, KLK6 immunoexpression was initially evaluated in normal tissues. We observed strong staining in the brain and moderate staining in the kidney, liver, and ovary, whereas the pancreas and the skeletal muscle were unreactive, which is in line with previously published results. Next, both tumor cell- and stromal cell-associated KLK6 immunoexpression were analyzed in tumor tissue specimens of 118 ovarian cancer patients. In multivariate Cox regression analysis, only stromal cell-associated expression, besides the established clinical parameters FIGO stage and residual tumor mass, was found to be statistically significant for OS and PFS [high vs. low KLK6 expression; hazard ratio (HR), 1.92; p=0.017; HR, 1.80; p=0.042, respectively]. These results indicate that KLK6 expressed by stromal cells may considerably contribute to the aggressiveness of ovarian cancer.
KW - Cancer biomarker
KW - Immunohistochemistry
KW - KLK6
KW - Kallikrein-related peptidase 6
KW - Ovarian cancer
KW - Prognosis
UR - https://www.scopus.com/pages/publications/84859827944
U2 - 10.1515/hsz-2011-0264
DO - 10.1515/hsz-2011-0264
M3 - Article
C2 - 22505521
AN - SCOPUS:84859827944
SN - 1431-6730
VL - 393
SP - 391
EP - 401
JO - Biological Chemistry
JF - Biological Chemistry
IS - 5
ER -