Article Data

  • Views 205
  • Dowloads 119

Original Research

Open Access

The effect of medroxyprogesterone acetate and norethisterone on the estradiol stimulated proliferation in MCF-7 cells: comparison of continuous combined versus sequential combined estradiol/progestin treatment

  • C. Lippert1
  • H. Seeger1
  • D. Wallwiener1
  • A. O. Mueck1,*,

1Centre for Endocrinology and Menopause, Department of Obstetrics and Gynaecology, University of Tuehingen, Tue bingen, Germany

DOI: 10.12892/ejgo200105331 Vol.22,Issue 5,September 2001 pp.331-335

Published: 10 September 2001

*Corresponding Author(s): A. O. Mueck E-mail: XXX

Abstract

Objective: Little is known on the type of progestin and regimen type in relation to breast cancer risk. We have compared the effect of medroxyprogesterone acetate (MPA) and norethisterone (NET) on the estradiol stimulated proliferation in MCF-7 cells with respect to different regimens used in combined hormone replacement therapy (HRT).

Design: To approximate the in vivo conditions in HRT, MCF-7 cultures were pretreated with estradiol followed by estradiol/progestin treatment to represent the sequential combined model and compared with non pretreated cultures followed by estradiol/progestin treatment for the continuous combined model.

Results: When using progestins in the continuous combined form with estradiol (10(-10) M) both progestins showed a significant reduction in the estradiol stimulated proliferation of the MCF-7 cells. In the sequential combined model the addition of MPA led to a stronger significant reduction of MCF-7 proliferation but in a narrower concentration range (from 10(-8) to 10(-6) M) compared to the continuous treatment. NET did not show any significant effect on proliferation in the SC model.

Conclusion: Different regimen types and different progestins do lead to significantly different effects on the proliferation of a breast cancer cell line. These findings might be useful in the elucidation of potential mechanisms involved in the clinical situation.

Keywords

Hormone replacement therapy; Medroxyprogesterone acetate; Norethisterone; MCF-7 cells; Regimen types

Cite and Share

C. Lippert,H. Seeger,D. Wallwiener,A. O. Mueck. The effect of medroxyprogesterone acetate and norethisterone on the estradiol stimulated proliferation in MCF-7 cells: comparison of continuous combined versus sequential combined estradiol/progestin treatment. European Journal of Gynaecological Oncology. 2001. 22(5);331-335.

References

[1] Schairer C., Lubin J., Troisi R., Sturgeon S., Brinton L., Hoover R.: "Menopausal estrogen and estrogen-progestin replacement therapy and breast cancer risk". JAMA, 2000, 283, 485.

[2] Ross R. K., Paganini-Hill A., Wan P. C., Pike M. C.: "Effect of hormone replacement therapy on breast cancer risk: estrogen versus estrogen plus progestin". J. Natl. Cancer Inst., 2000, 92, 328.

[3] Magnusson C., Baron J. A., Correia N., Bergstrom R., Adami H O., Persson I.: "Breast-cancer risk following long-term oestrogenand oestrogen-progestin-replacement therapy". Int. J. Cancer, 1999, 81, 339.

[4] Soule H. D., Vazquez J., Long A., Albert S., Brennan M.: "A human cell line from a pleural effusion derived from a breast carcinoma". J. Natl. Cancer Inst., 1973, 51, 1409.

[5] Pourreau-Schneider N., Martin P. M.. Charpin C.,J acquemier J., Saez S., Nandi S.: "How culture conditions modulate the morphofunctional differentiation of the human estradiol-sensitive mammary cell line (MCF-7)". J. Steroid. Biochem., 1984, 20, 407.

[6] Saceda M., Lippman M. E., Chambon P., Lindsey R. L., Ponglikitmongkol M., Puente M., Martin M. B.: "Regulation of the estrogen receptor in MCF-7 cells by estradiol". Mal. Endocrinology, 1988, 2, 1157.

[7] Katzenellenbogen B. S., Kendra K. L., Norman M. J., Bertho1s Y.: "Proliferation, hormonal responsiveness, and estrogen receptor content of MCF-7 human breast cancer cells grown in the short-term and long-term ab sense of estrogens". Cancer Res., 1987, 47, 4355.

[8] Schoonen W. G. E. J.、Joosten J. W. H., Klooosterboer H.J.: "Effects of two classes of progestagens pregnane and 19-nortestosterone derivatives, on cell growth of human breast tumor cells: I MCF-7 cell lines". J. Ster. Biochem. Mal. Biol., 1995, 55, 423.

[9] Kueng W., Silber E., Eppenberger U.: "Quantification of cells cultured on 96-well plates". Anal. Biochem., 1989, 82, 16.

[10] Collaborative Group on Hormonal Factors in Breast Cancer: "Breast cancer and hormone replacement therapy: collaborative reanalysis of data from 51 epidemiological studies of 52,705 women with breast cancer and 108,411 women without breast cancer". Lancet, 1997, 350, 1047.

[11] Ewertz M.: "Influence of non-contraceptive exogenous and endogenous sex hormones on breast cancer risk in Denmark". Int. J. Cancer, 1988, 42, 832.

[12] Husmann F.: "Hormone und Krebs: in wieweit erhi:ihen Estradiol und insbesondere Testosteron das Mammakarzinom-Risiko". Gyne., 1998, 11, 293.

[13] Doihara H., Takashima S., Saeki H., Takiyama W., Kurita A., Soga H. et al.: "Effect of medroxyprogesterone acetate on the cell kinetics in primary breast cancer". Gon To Kagaku Ryoho, 1990, 17, 2057.

[14] Sugiyama K., Shimizu M., Akiyama T., Ishida H., Okabe M., Tamaoki T., Akinaga S.: "Combined effect of navelbine with medroxyprogesterone acetate against human breast carcinoma MCF-7 cells in vitro". Brit. J. Cancer, 1998, 77, 1737.

[15] Sutherland R. L., HaII R. E., Pang G. Y., Musgrove E. A., Clarke C. L.: "Effect of medroxyprogesterone acetate on proliferation and cell cycle kinetics of human mammary cell". Cancer Res., 1988, 48, 5084.

[16] Cline J. M., Soderqvist G., von Schoultz E., Skoog L., von Schoultz B.: "Effects of hormone replacement therapy on the mammary gland of surgically postmenopausal cynomolgus macaques". Am. J. Obstet. Gynecol., 1996, 174, 93.

[17] Hofseth L. J., Raafat A. M., Osuch J. R., Pathak D. R., Slomski C A., Haslam S. Z.: "Hormone replacement therapy with estrogen or estrogen plus medroxyprogesterone acetate is associated with increased epithelial proliferation in the normal postmenopausal breast". J. Clin. Endocrin. Metab., 1999, 84, 4559.

[18] Catherino W. H.,J eng M. H.,J ordan V. C.: "Norgestrel and gestodene stimulate breast cancer cell growth through an oestrogen receptor mediated mechanism". Br. J. Cancer, 1993, 67, 945.

[19] Jeng M. H.,J ordan V. C.: "Growth stimulation and differential regulation of transforming growth factor-BI (TGFB I), TGFB2, and TGFB3 messenger RNA levels by norethindrone in MCF-7 human breast cancer cells". Mol. Endocr., 1991, 5, 1120.

[20] Clave! B., Pichon M. F., Pallud C., Milgrom E.: "Estradiol and progesterone receptors content and response to norethisterone treatment in advanced breast cancer". Eur. J. Cancer Clin. Oncol., 1982,18, 821.

[21] Svensson L. 0.,J ohnson S. H., Olsson S. E.: "Plasma concentrations of medroxyprogesterone acetate, estradiol and estrone following oral administraton of Klimaxil®, Trisequence®/Provera®, and Divina®. A randomised, single-blind, triple cross-over bioavailabilily study in menopausal women". Maturitas, 1994, 18, 229.

[22] Stanczyk F. Z., Brenner P. F., Mishell D. R., Ortiz A., Gentzschem E. K. E., Goebelsmann U.: "A radioimmunoassay for norethindrone (NET): measurement of serum net concentrations following ingestion of NET-containing oral contraceptive steroids". Contraception, 1978, 18, 615.

[23] Blossey H. C., Wander H. E., Koebberling J., Nagel G. A.: "Pharmakokinetic and pharmacodynamic basis for the treatment of metastatic breast cancer with high dose medroxyprogesterone acetate". Cancer, 1984, 54, 1208.

[24] Klehr-Bathmann I., Kuhl H.: "Formation of ethinylestradiol in postmenopausal women during continuous treatment with a combination of estradiol, estriol and norethisterone acetate". Maturitas, 1995, 21, 245.

[25] Andreasen E. E., Madsen L. G.. Jensen H. K.: "Absorption of norethisterone acetate from tablets with normal and coarse particle size". Ugeskr Laeger, 1989, 151, 1109.

[26] Grady T., Gebretsadik T., Kerlikowske L., Ernster V., Petitti D. "Hormone replacement therapy and endometrial cancer risk: A metaanalysis". Obstet. Gynecol., 1995, 85, 304

[27] Persson I., Adami H. 0., Berkvist L., Lindgren A., Petterson B: "Hoover Risk of endometrial cancer after treatment with oestrogens alone or in conjunction with progestogens: results of a prospective study". BMJ, 1989, 298, 147.

Abstracted / indexed in

Science Citation Index Expanded (SciSearch) Created as SCI in 1964, Science Citation Index Expanded now indexes over 9,500 of the world’s most impactful journals across 178 scientific disciplines. More than 53 million records and 1.18 billion cited references date back from 1900 to present.

Biological Abstracts Easily discover critical journal coverage of the life sciences with Biological Abstracts, produced by the Web of Science Group, with topics ranging from botany to microbiology to pharmacology. Including BIOSIS indexing and MeSH terms, specialized indexing in Biological Abstracts helps you to discover more accurate, context-sensitive results.

Google Scholar Google Scholar is a freely accessible web search engine that indexes the full text or metadata of scholarly literature across an array of publishing formats and disciplines.

JournalSeek Genamics JournalSeek is the largest completely categorized database of freely available journal information available on the internet. The database presently contains 39226 titles. Journal information includes the description (aims and scope), journal abbreviation, journal homepage link, subject category and ISSN.

Current Contents - Clinical Medicine Current Contents - Clinical Medicine provides easy access to complete tables of contents, abstracts, bibliographic information and all other significant items in recently published issues from over 1,000 leading journals in clinical medicine.

BIOSIS Previews BIOSIS Previews is an English-language, bibliographic database service, with abstracts and citation indexing. It is part of Clarivate Analytics Web of Science suite. BIOSIS Previews indexes data from 1926 to the present.

Journal Citation Reports/Science Edition Journal Citation Reports/Science Edition aims to evaluate a journal’s value from multiple perspectives including the journal impact factor, descriptive data about a journal’s open access content as well as contributing authors, and provide readers a transparent and publisher-neutral data & statistics information about the journal.

Submission Turnaround Time

Conferences

Top