Skip to main content

Advertisement

Log in

Cathepsin D Activity in Human Ovarian Tissues and Ovarian Carcinoma

  • Published:
The Journal of the Society for Gynecologic Investigation: JSGI Aims and scope Submit manuscript

Abstract

Objective

This study determined levels of cathepsin D activity in tissue components of normal human ovary to establish a basis for comparison with human ovarian adenocarcinomas.

Methods

Cathepsin D activity per mg tissue, per μg protein, and per μg DNA was determined in human ovarian tissues (cortex, follicle, corpus luteum, corpus albicans) from patients of various ages and during the menstrual cycle. Levels of cathepsin D activity were also determined in ovarian adenocarcinomas and other pathologic tissues.

Results

Cathepsin D levels (per mg tissue) were significantly greater (P <.001) in ovarian follicle and corpus luteum compared with cortex. Although there was not a clear correlation between enzyme activity in the cortex and day of the menstrual cycle or patient age, levels of enzyme activity appeared to decrease with each paramtter. Cathepsin D levels per mg tissue in ovarian adenocarcinoma were 40% higher than in postmenopausal ovarian cortex, but the difference was not statistically significant.

Conclusion

The diversity of cathepsin D levels in normal ovarian tissue compartments indicates that specific tissues must be used in comparisons with ovarian tumors.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Berek JS. Practical gynecologic oncology. Baltimore: Williams and Wilkins, 1989:327–90.

    Google Scholar 

  2. Liotta LA. Gene products which play a role in cancer invasion and metastasis. Breast Cancer Research and Treatment 1988;11:113–24.

    Article  CAS  Google Scholar 

  3. Ossowski L, Biegel D, Reich E. Mammary plasminogen activator: Correlation with involution, hormonal modulation and comparison between normal and neoplastic tissue. Cell 1979;16:929–40.

    Article  CAS  Google Scholar 

  4. Brule F, Engel J, Stetler W, Liu F, Sobel M. Genes involved in tumor invasion. Int J Cancer 1992;52:653–7.

    Article  Google Scholar 

  5. Leto G, Gebbia N, Rausa L, Tumminello FM. Cathepsin D in the malignant progression of neoplastic diseases (Review). Anticancer Research 1992;12:235–40.

    CAS  PubMed  Google Scholar 

  6. Astedt B, Holmberg L. Immunological identity of urokinase and ovarian carcinoma plasminogen activator released in tissue culture. Nature 1976;261:595–6.

    Article  CAS  Google Scholar 

  7. Astedt B, Svanberg L, Nilsson IM. Fibrin degradation products and ovarian tumours. Br Med J 1971;4:458–9.

    Article  CAS  Google Scholar 

  8. Kanemoto T, Martin GR, Hamilton TC, Fridman R. Effects of synthetic peptides and protease inhibitors on the interaction of a human ovarian cancer cell line (NIH: OVCAR-3) with a reconstituted basement membrane (Matrigel). Invasion Metastasis 1991;11:84–92.

    CAS  PubMed  Google Scholar 

  9. Spyratos F, Brouillet JP, Defrenne A, et al. Cathepsin D: An independent prognostic factor for metastasis of breast cancer. Lancet 1989;8672:1115–8.

    Article  Google Scholar 

  10. Tandon AK, Clark GM, Chamness GC, Chirgwin JM, McGuire WL. Cathepsin D and prognosis in breast cancer. N Engl J Med 1990;322:297–302.

    Article  CAS  Google Scholar 

  11. Scambia G, Benedetti P, Ferrandina G, Battaglia F, Baiocchi G, Mancuso S. Cathepsin D assay in ovarian cancer: Correlation with pathological features and receptors for oestrogen, progesterone and epidermal growth factor. Br J Cancer 1991;64:182–4.

    Article  CAS  Google Scholar 

  12. Dhanasekaran N, Moudgal NR. Studies on follicular atresia: Role of tropic hormone and steroids in regulating cathepsin-D activity of preantral follicles of the immature rat. Mol Cell Endocrinol 1986;44:77–84.

    Article  CAS  Google Scholar 

  13. Lahav M, Meidan R, Amsterdam A, Gebauer H, Lindner HR. Intracellular distribution of cathepsin D in rat corpora lutea in relation to reproductive state and the action of prostaglandin 2 Fα and prolactin. J Endocrinol 1977;75:317–24.

    Article  CAS  Google Scholar 

  14. Sensibar JA, Liu X, Patai B, Alger B, Lee C. Characterization of castration-induced cell death in the rat prostate by immunohistochemical localization of cathepsin D. Prostate 1990;16:263–76.

    Article  CAS  Google Scholar 

  15. Elangovan S, Moulton BC. Blastocyst implantation in the rat and the immunohistochemical distribution and rate of synthesis of uterine lysosomal cathepsin D. Biol Reprod 1981;23:663–76.

    Article  Google Scholar 

  16. Briozzo P, Morisset M, Capony F, Rougeot C, Rochefort H. In vitro degradation of extracellular matrix with Mr 52,000 cathepsin D secreted by breast cancer cells. Cancer Res 1988;48:3688–92.

    CAS  PubMed  Google Scholar 

  17. Leto G, Tumminello FM, Gebbia N, Woyrnarowska B, Bernacki RJ. Antimetastatic effects of adriamycin in combination with proteinase inhibitors. Anticancer Res 1990; 10:265–70.

    CAS  PubMed  Google Scholar 

  18. Mathieu M, Rochefort H, Barenton B, Prebois C, Vignon F. Interaction of cathepsin D and insulin-like growth factor II (IGF-II) on the IGF-II/mannose-6-phosphate receptor in human breast cancer cells and possible consequence on mitogenic activity of IGF-II. Mol Endocrinol 1990;4:1327–35.

    Article  CAS  Google Scholar 

  19. Greenbaum LM, Grebow P, Johnston M, Prakash A, Semente G. Pepstatin, an inhibitor of leukokinin formation and ascitic fluid accumulation. Cancer Res 1975;35:706–10.

    CAS  PubMed  Google Scholar 

  20. Greenbaum LM, Semente G. Pepstatin as ascites retardant of L1210 tumor bearing mice. J Natl Cancer Inst 1977;59: 259–62.

    Article  CAS  Google Scholar 

  21. Morisset M, Capony F, Rochefort H. Processing and estrogen regulation of the 52-kilodalton protein inside M7CF breast cancer cells. Endocrinology 1986;119:2773–82.

    Article  CAS  Google Scholar 

  22. Moulton BC, Koenig BB. Progestin increases cathepsin D synthesis in uterine luminal epithelial cells. Am J Physiol 1983;244:E442–6.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

This research was supported by grants from the American Cancer Society Ohio Division and from the National Institute of Child Health and Human Development (HD-00653).

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hradek, D.I., Kessel, B., Husseinzadeh, N. et al. Cathepsin D Activity in Human Ovarian Tissues and Ovarian Carcinoma. Reprod. Sci. 1, 173–177 (1994). https://doi.org/10.1177/107155769400100213

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1177/107155769400100213

Key words

Navigation