Polyclonal antibodies against kallikrein-related peptidase 4 (KLK4): immunohistochemical assessment of KLK4 expression in healthy tissues and prostate cancer

被引:33
|
作者
Seiz, Lina [1 ]
Kotzsch, Matthias [2 ]
Grebenchtchikov, Nicolai I. [3 ]
Geurts-Moespot, Anneke J. [3 ]
Fuessel, Susanne [4 ]
Goettig, Peter [5 ]
Gkazepis, Apostolos [1 ]
Wirth, Manfred P. [4 ]
Schmitt, Manfred [1 ]
Lossnitzer, Arndt [2 ]
Sweep, Fred C. G. J. [3 ]
Magdolen, Viktor [1 ]
机构
[1] Tech Univ Munich, Clin Res Unit, Dept Obstet & Gynecol, D-81675 Munich, Germany
[2] Tech Univ Dresden, Inst Pathol, D-01307 Dresden, Germany
[3] Radboud Univ Nijmegen, Med Ctr, Dept Lab Med, NL-6525 GA Nijmegen, Netherlands
[4] Tech Univ Dresden, Dept Urol, D-01307 Dresden, Germany
[5] Salzburg Univ, Struct Biol Grp, A-5020 Salzburg, Austria
关键词
immunohistochemistry; kallikrein-related peptidase 4; KLK4; prostase; prostate cancer; PLASMINOGEN-ACTIVATOR; SERINE-PROTEASE; BREAST-CANCER; UROKINASE; SPECIFICITY; RECEPTOR; CLONING; HK4;
D O I
10.1515/BC.2010.033
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
KLK4 is a member of the human kallikrein-related peptidase family of (chymo)trypsin-like serine proteases. The aim of the present study was to generate polyclonal antibodies (pAb) directed against KLK4 for the analysis of KLK4 by immunohistochemistry in human tissues. Recombinantly expressed human mature KLK4 was used for immunization of chickens. pAb 617A is an affinity-purified monospecific pAb fraction reacting with a linear epitope within a flexible surface-exposed loop of KLK4. pAb 617C is the KLK-directed pAb fraction completely depleted from pAb 617A. In healthy adult tissues, KLK4 was immunodetected by both antibody fractions in kidney, liver, and prostate, but not in other organs such as colon and lung. To evaluate protein expression of KLK4 in prostate cancer, samples of tumor tissue plus corresponding tumor-free areas of 44 prostate cancer patients, represented on a tissue microarray, were investigated. Distinct KLK4 immunostaining was observed with both antibodies in cancerous glandular epithelial cells, but not in surrounding stromal cells. KLK4 expression was lower in stage pT3+4 than in pT1+2 tumors, which was highly significant when employing pAb 617A. Thus, our results indicate that KLK4, which is expressed in the healthy prostate, is upregulated in early-stage but not late-stage prostate cancer.
引用
收藏
页码:391 / 401
页数:11
相关论文
共 50 条
  • [11] Kallikrein-related peptidase 4 (KLK4) initiates intracellular signaling via protease-activated receptors (PARs)
    Ramsay, Andrew J.
    Dong, Ying
    Hunt, Melanie L.
    Linn, Mayla
    Samaratunga, Hemamali
    Clements, Judith A.
    Hooper, John D.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (18) : 12293 - 12304
  • [12] Characterization of kallikrein-related peptidase 4 (KLK4) mRNA expression in tumor tissue of advanced high-grade serous ovarian cancer patients
    Gong, Weiwei
    Liu, Yueyang
    Seidl, Christof
    Dreyer, Tobias
    Drecoll, Enken
    Kotzsch, Matthias
    Bronger, Holger
    Dorn, Julia
    Magdolen, Viktor
    PLOS ONE, 2019, 14 (02):
  • [13] Characterization of KLK4 expression and detection of KLK4-specific antibody in prostate cancer patient sera
    Day, CH
    Fanger, GR
    Retter, MW
    Hylander, BL
    Penetrante, RB
    Houghton, RL
    Zhang, XQ
    McNeill, PD
    Maltez, A
    Nolasco, M
    Badaro, R
    Cheever, MA
    Reed, SG
    Dillon, DC
    Watanabe, Y
    ONCOGENE, 2002, 21 (46) : 7114 - 7120
  • [14] Characterization of KLK4 expression and detection of KLK4-specific antibody in prostate cancer patient sera
    Craig H Day
    Gary R Fanger
    Marc W Retter
    Bonnie L Hylander
    Remedios B Penetrante
    Raymond L Houghton
    Xinqun Zhang
    Patricia D McNeill
    Aristides Maltez Filho
    Marcos Nolasco
    Roberto Badaro
    Martin A Cheever
    Steven G Reed
    Davin C Dillon
    Yoshihiro Watanabe
    Oncogene, 2002, 21 : 7114 - 7120
  • [15] Significant alterations in the expression pattern of kallikrein-related peptidase genes KLK4, KLK5 and KLK14 after treatment of breast cancer cells with the chemotherapeutic agents epirubicin, docetaxel and methotrexate
    Papachristopoulou, Georgia
    Talieri, Maroulio
    Scorilas, Andreas
    TUMOR BIOLOGY, 2013, 34 (01) : 369 - 378
  • [16] Genetic Association of the KLK4 Locus with Risk of Prostate Cancer
    Lose, Felicity
    Srinivasan, Srilakshmi
    O'Mara, Tracy
    Marquart, Louise
    Chambers, Suzanne
    Gardiner, Robert A.
    Aitken, Joanne F.
    Spurdle, Amanda B.
    Batra, Jyotsna
    Clements, Judith A.
    PLOS ONE, 2012, 7 (09):
  • [17] KLK4 in luminal breast cancer progression
    Fuentes, P.
    Ramos, I.
    Stuardo, A.
    Diaz, F.
    Sanchez, F.
    Torres, C.
    Rojas, A.
    Maldonado, R.
    Cordova, L.
    Burgos, P. V.
    Pavicic, F.
    Figueroa, C.
    Ehrenfeld, P.
    BREAST, 2023, 68 : S29 - S29
  • [18] Compartmentalized expression of kallikrein 4 (KLK4/hK4) isoforms in prostate cancer:: nuclear, cytoplasmic and secreted forms
    Dong, Y
    Bui, LT
    Odorico, DM
    Tan, OL
    Myers, SA
    Samaratunga, H
    Gardiner, RA
    Clements, JA
    ENDOCRINE-RELATED CANCER, 2005, 12 (04) : 875 - 889
  • [19] Low mRNA expression levels of kallikrein-related peptidase 4 (KLK4) predict short-term relapse in patients with laryngeal squamous cell carcinoma
    Foteinou, Emmanouela
    Kontos, Christos K.
    Giotakis, Aris I.
    Scorilas, Andreas
    BIOLOGICAL CHEMISTRY, 2014, 395 (09) : 1051 - 1062
  • [20] Human kallikrein 4 (KLK4) is highly expressed in serous ovarian carcinomas
    Dong, Y
    Kaushal, A
    Bui, L
    Chu, S
    Fuller, PJ
    Nicklin, J
    Samaratunga, H
    Clements, JA
    CLINICAL CANCER RESEARCH, 2001, 7 (08) : 2363 - 2371