Cancer Research Infection and Cancer: Biology, Therapeutics, and Prevention
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

[Cancer Research 56, 5397-5402, December 1, 1996]
© 1996 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kumar, A.
Right arrow Articles by Saedi, M. S.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kumar, A.
Right arrow Articles by Saedi, M. S.

Expression of Human Glandular Kallikrein, hK2, in Mammalian Cells

Abhay Kumar, Amita S. Goel, Timothy M. Hill, Stephen D. Mikolajczyk, Lisa S. Millar, Kristine Kuus-Reichel and Mohammad S. Saedi1

Hybritech Incorporated, San Diego, California 92196-9006

The human kallikrein family consists of three members, hK1, hK2, and hK3 [prostate-specific antigen (PSA)]. PSA is a widely accepted marker for prostate cancer. The mRNAs for both hK2 and PSA are localized predominantly to prostate epithelium and are regulated by androgens. In addition, hK2 has 78% amino acid homology to PSA. Although similarities to PSA make hK2 a potential prostate cancer marker, they also impede biochemical characterization of hK2 in those human tissues and body fluids where PSA is abundant. To study the expression, biosynthesis, and processing of hK2, recombinant hK2 was expressed in the adenovirus-induced Syrian hamster tumor cell line AV12-664 (AV12-hK2). Expression of hK2 was analyzed by Western blots and ELISA using monoclonal antibodies HK1G 464.3 [specific for prohK2 (phK2)] and HK1D 106.4 [specific for phK2 and mature hK2 (hK2)]. Western blot and ELISA analyses showed that phK2 was secreted into the media by AV12-hK2 cells on day 1 and was gradually converted to the mature form of hK2 by day 7. N-terminal amino acid sequencing verified the Western blot and ELISA data. This demonstrates for the first time that hK2 is secreted as phK2 and converted to hK2 extracellularly. In addition, hK2 detected in day 4–7 AV12-hK2-spent media was enzymatically active. Recombinant hK2 was also expressed in human prostate carcinoma cell lines, PC3 (PC3-hK2) and DU145 (DU145-hK2), that do not express endogenous hK2 or PSA. Similar to AV12-hK2 cells, both cell lines secreted phK2 that was converted to hK2 extracellularly. phK2 was the major form detected in the spent media of PC3-hK2 cells, even after 7 days, indicating a slow conversion of phK2 to hK2. hK2 was the predominant form detected in the spent media of DU145-hK2 starting on day 1, indicating the rapid conversion of phK2 to hK2. In this study, we demonstrate that hK2 exists in different forms and is secreted as phK2. phK2 is then converted to enzymatically active hK2 extracellularly.

1 To whom requests for reprints should be addressed, at Hybritech Incorporated, Box 269006, San Diego, CA 92196-9006. Phone: (619) 535-8706; Fax: (619) 457-5308; E-mail: ADMS@Beckman.com.

Received 5/13/96. Accepted 10/16/96.




This article has been cited by other articles:


Home page
Cancer Res.Home page
S. D. Mikolajczyk, K. M. Marker, L. S. Millar, A. Kumar, M. S. Saedi, J. K. Payne, C. L. Evans, C. L. Gasior, H. J. Linton, P. Carpenter, et al.
A Truncated Precursor Form of Prostate-specific Antigen Is a More Specific Serum Marker of Prostate Cancer
Cancer Res., September 1, 2001; 61(18): 6958 - 6963.
[Abstract] [Full Text] [PDF]


Home page
Clin. Chem.Home page
J. A. Finlay, J. R. Day, C. L. Evans, R. Carlson, K. Kuus-Reichel, L. S. Millar, S. D. Mikolajczyk, M. Goodmanson, G. G. Klee, and H. G. Rittenhouse
Development of a Dual Monoclonal Antibody Immunoassay for Total Human Kallikrein 2
Clin. Chem., July 1, 2001; 47(7): 1218 - 1224.
[Abstract] [Full Text] [PDF]


Home page
Endocr. Rev.Home page
G. M. Yousef and E. P. Diamandis
The New Human Tissue Kallikrein Gene Family: Structure, Function, and Association to Disease
Endocr. Rev., April 1, 2001; 22(2): 184 - 204.
[Abstract] [Full Text]


Home page
Clin. Chem.Home page
A. Magklara, A. Scorilas, C. Lopez-Otin, F. Vizoso, A. Ruibal, and E. P. Diamandis
Human Glandular Kallikrein in Breast Milk, Amniotic Fluid, and Breast Cyst Fluid
Clin. Chem., October 1, 1999; 45(10): 1774 - 1780.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
S. D. Mikolajczyk, L. S. Millar, K. M. Marker, H. G. Rittenhouse, R. L. Wolfert, L. S. Marks, M. C. Charlesworth, and D. J. Tindall
Identification of a Novel Complex between Human Kallikrein 2 and Protease Inhibitor-6 in Prostate Cancer Tissue
Cancer Res., August 1, 1999; 59(16): 3927 - 3930.
[Abstract] [Full Text] [PDF]


Home page
EndocrinologyHome page
S. Zhang, M.-L. Hsieh, W. Zhu, G. G. Klee, D. J. Tindall, and C. Y. F. Young
Interactive Effects of Triiodothyronine and Androgens on Prostate Cell Growth and Gene Expression
Endocrinology, April 1, 1999; 140(4): 1665 - 1671.
[Abstract] [Full Text]


Home page
Clin. Chem.Home page
M. S. Saedi, T. M. Hill, K. Kuus-Reichel, A. Kumar, J. Payne, S. D. Mikolajczyk, R. L. Wolfert, and H. G. Rittenhouse
The precursor form of the human kallikrein 2, a kallikrein homologous to prostate-specific antigen, is present in human sera and is increased in prostate cancer and benign prostatic hyperplasia
Clin. Chem., October 1, 1998; 44(10): 2115 - 2119.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
L. Bourgeois, M. Brillard-Bourdet, D. Deperthes, M. A. Juliano, L. Juliano, R. R. Tremblay, J. Y. Dube, and F. Gauthier
Serpin-derived Peptide Substrates for Investigating the Substrate Specificity of Human Tissue Kallikreins hK1 and hK2
J. Biol. Chem., November 21, 1997; 272(47): 29590 - 29595.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1996 by the American Association for Cancer Research.