| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, Ontario M5G 1X5, Canada [H. Y., E. P. D., M. L., S. L. A.]; Department of Clinical Biochemistry, University of Toronto, Toronto, Ontario M5G 1L5, Canada [H. Y., E. P. D., M. L.]; Department of Pathology, University of Toronto, Toronto, Ontario M5G 1L3, Canada [E. P. D., S. L. A.]; and Department of Microbiology-Immunology, Jefferson Cancer Institute, Thomas Jefferson University, Philadelphia, Pennsylvania 19107 [M. M., C. M. C.]
We describe a patient with primary ovarian carcinoma that developed after liver transplantation whose tumor was highly positive for prostate-specific antigen (PSA). PSA in tumor tissue was characterized by two immunoassays, HPLC, immunohistochemistry, reverse transcription-PCR, Southern blotting, and DNA sequencing. PSA in the ovarian tumor was present as free, Mr 33,000 protein (>90%) and as PSA bound to
1-antichymotrypsin (Mr 100,000; <10%). Immunohistochemistry localized PSA in the cytoplasm of epithelial cells of the tumor. Two separate reverse transcription-PCRs for PSA amplified the expected products which hybridized specifically to a PSA cDNA probe on Southern blots. Sequencing of the PCR products, representing the whole coding sequence of the PSA gene, revealed identity with the sequence of PSA cDNA from prostate tissue. These data suggest that the PSA produced by the ovarian tumor was identical in molecular weight and sequence to prostatic PSA. Based on data of tissue culture experiments with breast carcinoma cell lines, we speculate that the PSA gene in the tumor of this patient was up-regulated by the therapeutically administered glucocorticoids after liver transplantation.
1 This work was supported by a grant from the Ontario Section of the Canadian Breast Cancer Foundation (to E. P. D.).
2 To whom requests for reprints should be addressed, at Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, 600 University Ave., Toronto, Ontario, Canada M5G 1X5.
Received 1/30/95. Accepted 3/ 3/95.
This article has been cited by other articles:
![]() |
C. V. Obiezu, A. Scorilas, D. Katsaros, M. Massobrio, G. M. Yousef, S. Fracchioli, I. A. Rigault de la Longrais, R. Arisio, and E. P. Diamandis Higher Human Kallikrein Gene 4 (KLK4) Expression Indicates Poor Prognosis of Ovarian Cancer Patients Clin. Cancer Res., August 1, 2001; 7(8): 2380 - 2386. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Lopez-Otin and E. P. Diamandis Breast and Prostate Cancer: An Analysis of Common Epidemiological, Genetic, and Biochemical Features Endocr. Rev., August 1, 1998; 19(4): 365 - 396. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Mannello, M. Sebastiani, S. Amati, and G. Gazzanelli Prostate-specific antigen expression in a case of intracystic carcinoma of the breast: characterization of immunoreactive protein and literature surveys Clin. Chem., August 1, 1997; 43(8): 1448 - 1454. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. N. Melegos, H. Yu, M. Ashok, C. Wang, F. Stanczyk, and E. P. Diamandis Prostate-Specific Antigen in Female Serum, a Potential New Marker of Androgen Excess J. Clin. Endocrinol. Metab., March 1, 1997; 82(3): 777 - 780. [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 |