help button home button Am J Pathol ASIP WHAT IS IT?
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
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 Akoum, A.
Right arrow Articles by Khandjian, E. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Akoum, A.
Right arrow Articles by Khandjian, E. W.
(American Journal of Pathology. 1999;154:1245-1257.)
© 1999 American Society for Investigative Pathology


Regular Articles

Physiological and Cytogenetic Characterization of Immortalized Human Endometriotic Cells Containing Episomal Simian Virus 40 DNA

Ali Akoum* , Josée Lavoie{dagger} , Régen Drouin{dagger} , Christine Jolicoeur* , André Lemay* , Rodolphe Maheux* and Edouard W. Khandjian{dagger}

From the Laboratoire d'Endocrinologie de la Reproduction* and Unité de Recherche en Génétique Humaine et Moléculaire,{dagger} Centre de Recherche, Pavillon Saint-François d'Assise, Centre Hospitalier Universitaire de Québec, Université Laval, Québec, Canada

The study of misplaced endometrial cells, which abnormally implant and grow outside the uterine cavity, is of considerable interest for the understanding of the pathophysiology of endometriosis. However, endometriotic cells, particularly epithelial cells, required for primary cell culture are not easily available. We report here the characterization of an endometriotic cell line immortalized after infection of primary endometriotic cell cultures with simian virus 40. Transformed cells express T-antigen, and blot hybridization analysis showed that the viral genome is present as an episome. Cytogenetic analysis revealed a polyploid karyotype with numerical and structural rearrangements involving mainly the same chromosomes (6, 10, 11, 15, and 17). The cell line has been maintained in culture for over 80 passages and was still proliferating without any noticeable change in the biological properties investigated. Transformed endometriotic cells expressed both progesterone and estradiol receptors and were stimulated by these ovarian hormones to secrete monocyte chemotactic protein-1, a factor that may play an important role in the recruitment and activation of peritoneal macrophages. In addition, this response was enhanced in interleukin-1-treated cells. Taken together, these findings support the view that this cell line may be an interesting tool for the study of the pathophysiology of endometriosis.





This article has been cited by other articles:


Home page
Cancer Res.Home page
L. Ricciardiello, M. Baglioni, C. Giovannini, M. Pariali, G. Cenacchi, A. Ripalti, M. P. Landini, H. Sawa, K. Nagashima, R. J. Frisque, et al.
Induction of Chromosomal Instability in Colonic Cells by the Human Polyomavirus JC Virus
Cancer Res., November 1, 2003; 63(21): 7256 - 7262.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Pathol.Home page
A. Zeitvogel, R. Baumann, and A. Starzinski-Powitz
Identification of an Invasive, N-Cadherin-Expressing Epithelial Cell Type in Endometriosis Using a New Cell Culture Model
Am. J. Pathol., November 1, 2001; 159(5): 1839 - 1852.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
Y. Yang, P. Degranpré, A. Kharfi, and A. Akoum
Identification of Macrophage Migration Inhibitory Factor as a Potent Endothelial Cell Growth-Promoting Agent Released by Ectopic Human Endometrial Cells
J. Clin. Endocrinol. Metab., December 1, 2000; 85(12): 4721 - 4727.
[Abstract] [Full Text]


Home page
Proc. Natl. Acad. Sci. USAHome page
M. Bocchetta, I. Di Resta, A. Powers, R. Fresco, A. Tosolini, J. R. Testa, H. I. Pass, P. Rizzo, and M. Carbone
Human mesothelial cells are unusually susceptible to simian virus 40-mediated transformation and asbestos cocarcinogenicity
PNAS, August 17, 2000; (2000) 170207097.
[Abstract] [Full Text]


Home page
Reproductive SciencesHome page
J. Gogusev, J. B. de Joliniere, L. Telvi, M. Doussau, A. Stojkoski, and M. Levradon
Cellular and Genetic Constitution of Human Endometriosis Tissues
Reproductive Sciences, March 1, 2000; 7(2): 79 - 87.
[Abstract] [PDF]


Home page
CarcinogenesisHome page
J. S. Butel
Viral carcinogenesis: revelation of molecular mechanisms and etiology of human disease
Carcinogenesis, March 1, 2000; 21(3): 405 - 426.
[Abstract] [Full Text] [PDF]


Home page
JNCI J Natl Cancer InstHome page
J. S. Butel and J. A. Lednicky
RESPONSE: Re: Cell and Molecular Biology of Simian Virus 40: Implications for Human Infections and Disease
J Natl Cancer Inst, July 7, 1999; 91(13): 1166a - 1167a.
[Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
M. Bocchetta, I. Di Resta, A. Powers, R. Fresco, A. Tosolini, J. R. Testa, H. I. Pass, P. Rizzo, and M. Carbone
From the Cover: Human mesothelial cells are unusually susceptible to simian virus 40-mediated transformation and asbestos cocarcinogenicity
PNAS, August 29, 2000; 97(18): 10214 - 10219.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1999 by the American Society for Investigative Pathology.