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

This Article
Right arrow Order Full text via Infotrieve
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 Gompel, A.
Right arrow Articles by Poitout, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Gompel, A.
Right arrow Articles by Poitout, P.

American Journal of Pathology, Vol 144, 1195-1202, Copyright © 1994 by American Society for Investigative Pathology


REGULAR ARTICLES

Bcl-2 expression in normal endometrium during the menstrual cycle

A Gompel, JC Sabourin, A Martin, H Yaneva, J Audouin, Y Decroix and P Poitout
Departement de Gynecologie et Obstetrique, Hopital Hotel Dieu, Paris, France.

Bcl-2 is a proto-oncogene initially described in the (14;18) translocation in follicular lymphoma. It has been shown to prolong cell survival by preventing apoptosis. Endometrium undergoes rapid proliferation and differentiation under hormone control and is thus an excellent model to study the hormone dependency of Bcl-2 expression. We studied Bcl-2 expression by an immunohistochemical method in 53 samples of normal endometrium randomly distributed throughout the menstrual cycle, as well as five samples of hyperplastic endometrium. Bcl-2 staining predominated in glandular cells and peaked at the end of the follicular phase. Bcl-2 expression disappeared at the onset of secretory activity. The stroma, surface lining epithelium and arterial vessels also displayed cyclic variations in Bcl-2 expression. These results strongly suggest hormone-dependent regulation of Bcl-2 expression, which could play an important role in tumorigenesis.


This article has been cited by other articles:


Home page
J. Clin. Endocrinol. Metab.Home page
P. Yin, Z. Lin, Y.-H. Cheng, E. E. Marsh, H. Utsunomiya, H. Ishikawa, Q. Xue, S. Reierstad, J. Innes, S. Thung, et al.
Progesterone Receptor Regulates Bcl-2 Gene Expression through Direct Binding to Its Promoter Region in Uterine Leiomyoma Cells
J. Clin. Endocrinol. Metab., November 1, 2007; 92(11): 4459 - 4466.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
A. Li, J.C. Felix, J. Hao, P. Minoo, and J.K. Jain
Menstrual-like breakdown and apoptosis in human endometrial explants
Hum. Reprod., June 1, 2005; 20(6): 1709 - 1719.
[Abstract] [Full Text] [PDF]


Home page
Hum Reprod UpdateHome page
T. Harada, A. Kaponis, T. Iwabe, F. Taniguchi, G. Makrydimas, N. Sofikitis, M. Paschopoulos, E. Paraskevaidis, and N. Terakawa
Apoptosis in human endometrium and endometriosis
Hum. Reprod. Update, January 1, 2004; 10(1): 29 - 38.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
E. Chatzaki, E. Kouimtzoglou, A.N. Margioris, and A. Gravanis
Transforming growth factor {beta}1 exerts an autocrine regulatory effect on human endometrial stromal cell apoptosis, involving the FasL and Bcl-2 apoptotic pathways
Mol. Hum. Reprod., February 1, 2003; 9(2): 91 - 95.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
E. Chatzaki, A. Makrigiannakis, A.N. Margioris, E. Kouimtzoglou, and A. Gravanis
The Fas/FasL apoptotic pathway is involved in {kappa}-opioid-induced apoptosis of human endometrial stromal cells
Mol. Hum. Reprod., September 1, 2001; 7(9): 867 - 874.
[Abstract] [Full Text] [PDF]


Home page
Obstet GynecolHome page
H. A. ARANGO, S. ICELY, W. S. ROBERTS, D. CAVANAGH, and J. L. BECKER
Aspirin Effects on Endometrial Cancer Cell Growth
Obstet. Gynecol., March 1, 2001; 97(3): 423 - 427.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
R. Konno, H. Yamakawa, H. Utsunomiya, K. Ito, S. Sato, and A. Yajima
Expression of survivin and Bcl-2 in the normal human endometrium
Mol. Hum. Reprod., June 1, 2000; 6(6): 529 - 534.
[Abstract] [Full Text] [PDF]


Home page
Obstet GynecolHome page
Y. MATSUMOTO, T. IWASAKA, F. YAMASAKI, and H. SUGIMORI
Apoptosis and Ki-67 Expression in Adenomyotic Lesions and in the Corresponding Eutopic Endometrium
Obstet. Gynecol., July 1, 1999; 94(1): 71 - 77.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
M. Dahmoun, K. Boman, S. Cajander, P. Westin, and T. Bäckström
Apoptosis, Proliferation, and Sex Hormone Receptors in Superficial Parts of Human Endometrium at the End of the Secretory Phase
J. Clin. Endocrinol. Metab., May 1, 1999; 84(5): 1737 - 1743.
[Abstract] [Full Text]


Home page
Am. J. Respir. Cell Mol. Bio.Home page
J. Tesfaigzi, J. A. Hotchkiss, and J. R. Harkema
Expression of the Bcl-2 Protein in Nasal Epithelia of F344/N Rats during Mucous Cell Metaplasia and Remodeling
Am. J. Respir. Cell Mol. Biol., June 1, 1998; 18(6): 794 - 799.
[Abstract] [Full Text]


Home page
J. Clin. Endocrinol. Metab.Home page
X.-J. Tao, K. I. Tilly, D. V. Maravei, J. L. Shifren, S. Krajewski, J. C. Reed, J. L. Tilly, and K. B. Isaacson
Differential Expression of Members of the bcl-2 Gene Family in Proliferative and Secretory Human Endometrium: Glandular Epithelial Cell Apoptosis Is Associated with Increased Expression of bax
J. Clin. Endocrinol. Metab., August 1, 1997; 82(8): 2738 - 2746.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
A. Pecci, A. Scholz, D. Pelster, and M. Beato
Progestins Prevent Apoptosis in a Rat Endometrial Cell Line and Increase the Ratio of bcl-XL to bcl-XS
J. Biol. Chem., May 2, 1997; 272(18): 11791 - 11798.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
H. Matsuo, T. Maruo, and T. Samoto
Increased Expression of Bcl-2 Protein in Human Uterine Leiomyoma and Its Up-Regulation by Progesterone
J. Clin. Endocrinol. Metab., January 1, 1997; 82(1): 293 - 299.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1994 by the American Society for Investigative Pathology.