Carcinogenesis, Vol. 20, No. 11, 2057-2061,
November 1999
© 1999 Oxford University Press
Cancer Biology |
Effects of environmental estrogens on tumor necrosis factor
-mediated apoptosis in MCF-7 cells
1 Molecular and Cellular Biology Program,
2 Department of Pharmacology,
3 Tulane-Xavier Center for Bioenvironmental Research,
4 Tulane Cancer Center and
5 Department of Environmental Health Sciences, Tulane University School of Medicine, New Orleans, LA 70112 and
6 The Burnham Institute, La Jolla, CA 92037-1062, USA
Environmental estrogens represent a class of compounds which have been shown to mimic the effects or activity of the naturally occurring ovarian hormone 17ß-estradiol. Given the role of 17ß-estradiol in cell survival in a number of systems, we wished to determine if environmental estrogens protect MCF-7 cells from apoptosis. Here we demonstrate that the organochlorine pesticides o, p' DDT and alachlor, like 17ß-estradiol, have the ability to suppress tumor necrosis factor
(TNF)-induced apoptosis in estrogen receptor (ER)-positive MCF-7 breast carcinoma cells. These compounds, however, did not affect TNF-induced apoptosis of the ER-negative MDA-MB-231 cell line. The ability of these compounds to suppress apoptosis in MCF-7 cells was correlated with an ER-dependent increase in Bcl-2 expression. Taken together these results demonstrate that estrogenic organochlorine pesticides like o, p' DDT and alachlor may partially mimic the primary endogenous estrogen, 17ß-estradiol, and function to suppress apoptosis in ER-responsive cells.
Abbreviations: alachlor, 2-chloro-N-(2,6-diethylphenyl)-N-(methoxymethyl)acetamide; o,p' DDT, 1,1,1-trichloro-2-(p-chlorophenyl)-2-(o-chlorophenyl) ethane; DMEM, Dulbecco's modified Eagle's medium; endosulfan II (3
,5aß,6ß,9ß,9aß)-6,7,8,9,10,10-hexachloro-1,5,5a,6,9,9a-hexahydro-6,9-methano-2,4,3-benzodioxathiepin 3-oxide: ER, estrogen receptor; ERE, estrogen response element; FBS, fetal bovine serum; TNF, tumor necrosis factor
.
7 To whom correspondence should be addressed at: Tulane University Medical Center, Department of Pharmacology SL-83, 1430 Tulane Avenue, New Orleans, LA 70112, USA Email: bbeckman{at}tmcpop.tmc.tulane.edu
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
S. M. Boue, S. L. Tilghman, S. Elliott, M. C. Zimmerman, K. Y. Williams, F. Payton-Stewart, A. P. Miraflor, M. H. Howell, B. Y. Shih, C. H. Carter-Wientjes, et al. Identification of the Potent Phytoestrogen Glycinol in Elicited Soybean (Glycine max) Endocrinology, May 1, 2009; 150(5): 2446 - 2453. [Abstract] [Full Text] [PDF] |
||||
![]() |
X. Zhao and P. Lacasse Mammary tissue damage during bovine mastitis: Causes and control J Anim Sci, March 1, 2008; 86(13_suppl): 57 - 65. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. N. Duong, S. Elliott, D. E. Frigo, L. I. Melnik, L. Vanhoy, S. Tomchuck, H. P. Lebeau, O. David, B. S. Beckman, J. Alam, et al. AKT Regulation of Estrogen Receptor {beta} Transcriptional Activity in Breast Cancer. Cancer Res., September 1, 2006; 66(17): 8373 - 8381. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. I. Fernando and J. Wimalasena Estradiol Abrogates Apoptosis in Breast Cancer Cells through Inactivation of BAD: Ras-dependent Nongenomic Pathways Requiring Signaling through ERK and Akt Mol. Biol. Cell, July 1, 2004; 15(7): 3266 - 3284. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Simstein, M. Burow, A. Parker, C. Weldon, and B. Beckman Apoptosis, Chemoresistance, and Breast Cancer: Insights From the MCF-7 Cell Model System Experimental Biology and Medicine, October 1, 2003; 228(9): 995 - 1003. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. J. Kottke, A. L. Blajeski, X. W. Meng, P. A. Svingen, S. Ruchaud, P. W. Mesner Jr., S. A. Boerner, K. Samejima, N. V. Henriquez, T. J. Chilcote, et al. Lack of Correlation between Caspase Activation and Caspase Activity Assays in Paclitaxel-treated MCF-7 Breast Cancer Cells J. Biol. Chem., January 4, 2002; 277(1): 804 - 815. [Abstract] [Full Text] |
||||
![]() |
J. A. McLachlan Environmental Signaling: What Embryos and Evolution Teach Us About Endocrine Disrupting Chemicals Endocr. Rev., June 1, 2001; 22(3): 319 - 341. [Abstract] [Full Text] [PDF] |
||||






