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Olfactomedin-4 regulation by estrogen in the human endometrium requires epidermal growth factor signaling

(2010) AMERICAN JOURNAL OF PATHOLOGY. 177(5). p.2495-2508
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Abstract
Olfactomedin-4 (OLFM-4) is an extracellular matrix protein that is highly expressed in human endometrium. We have examined the regulation and function of OLFM-4 in normal endometrium and in cases of endometriosis and endometrial cancer. OLFM-4 expression levels are highest in proliferative-phase endometrium, and 17 beta-estradiol up-regulates OLFM-4 mRNA in endometrial explant cultures. Using the luciferase reporter under control of the OLFM-4 promoter, it was shown that both 17 beta-estradiol and OH-tamoxifen induce luciferase activity, and epidermal growth factor receptor-1 is required for this estrogenic response. In turn, EGF activates the OLFM-4 promoter, and estrogen receptor-alpha is needed for the complete EGF response. The cellular functions of OLFM-4 were examined by its expression in OLFM-4-negative HEK-293 cells, which resulted in decreased vimentin expression and cell adherence as well as increased apoptosis resistance. In cases of endometriosis and endometrial cancer, OLFM-4 expression correlated with the presence of epidermal growth factor receptor-1 and estrogen receptor-alpha (or estrogen signaling). An increase of OLFM-4 mRNA was observed in the endometrium of endometriosis patients. No change in OLFM-4 expression levels were observed in patients with endometrial cancer relative with controts. In conclusion, cross-talk between estrogen and EGF signaling regulates OLFM-4 expression. The role of OLFM-4 in endometrial tissue remodeling before the secretory phase and during the predisposition and early events in endometriosis can be postulated but requires additional investigation.
Keywords
PROTEIN, RECEPTOR, CELLS, CANCER, HGC-1, KINASE, SERIAL ANALYSIS, GASTRIC-CARCINOMA, MENSTRUAL-CYCLE, GENE-EXPRESSION

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MLA
DASSEN, HELEN, et al. “Olfactomedin-4 Regulation by Estrogen in the Human Endometrium Requires Epidermal Growth Factor Signaling.” AMERICAN JOURNAL OF PATHOLOGY, vol. 177, no. 5, 2010, pp. 2495–508, doi:10.2353/ajpath.2010.100026.
APA
DASSEN, H., Punyadeera, C., Delvoux, B., Schulkens, I., Marchetti, C., Kamps, R., … Romano, A. (2010). Olfactomedin-4 regulation by estrogen in the human endometrium requires epidermal growth factor signaling. AMERICAN JOURNAL OF PATHOLOGY, 177(5), 2495–2508. https://doi.org/10.2353/ajpath.2010.100026
Chicago author-date
DASSEN, HELEN, Chamindie Punyadeera, Bert Delvoux, Iris Schulkens, Claudia Marchetti, Rick Kamps, Jan Klomp, et al. 2010. “Olfactomedin-4 Regulation by Estrogen in the Human Endometrium Requires Epidermal Growth Factor Signaling.” AMERICAN JOURNAL OF PATHOLOGY 177 (5): 2495–2508. https://doi.org/10.2353/ajpath.2010.100026.
Chicago author-date (all authors)
DASSEN, HELEN, Chamindie Punyadeera, Bert Delvoux, Iris Schulkens, Claudia Marchetti, Rick Kamps, Jan Klomp, Fred Dijcks, Anton de Goeij, Thomas D’Hooghe, Cleophas Kyama, Antwan Ederveen, Gerard Dunselman, Patrick Groothuis, and Andrea Romano. 2010. “Olfactomedin-4 Regulation by Estrogen in the Human Endometrium Requires Epidermal Growth Factor Signaling.” AMERICAN JOURNAL OF PATHOLOGY 177 (5): 2495–2508. doi:10.2353/ajpath.2010.100026.
Vancouver
1.
DASSEN H, Punyadeera C, Delvoux B, Schulkens I, Marchetti C, Kamps R, et al. Olfactomedin-4 regulation by estrogen in the human endometrium requires epidermal growth factor signaling. AMERICAN JOURNAL OF PATHOLOGY. 2010;177(5):2495–508.
IEEE
[1]
H. DASSEN et al., “Olfactomedin-4 regulation by estrogen in the human endometrium requires epidermal growth factor signaling,” AMERICAN JOURNAL OF PATHOLOGY, vol. 177, no. 5, pp. 2495–2508, 2010.
@article{1843480,
  abstract     = {{Olfactomedin-4 (OLFM-4) is an extracellular matrix protein that is highly expressed in human endometrium. We have examined the regulation and function of OLFM-4 in normal endometrium and in cases of endometriosis and endometrial cancer. OLFM-4 expression levels are highest in proliferative-phase endometrium, and 17 beta-estradiol up-regulates OLFM-4 mRNA in endometrial explant cultures. Using the luciferase reporter under control of the OLFM-4 promoter, it was shown that both 17 beta-estradiol and OH-tamoxifen induce luciferase activity, and epidermal growth factor receptor-1 is required for this estrogenic response. In turn, EGF activates the OLFM-4 promoter, and estrogen receptor-alpha is needed for the complete EGF response. The cellular functions of OLFM-4 were examined by its expression in OLFM-4-negative HEK-293 cells, which resulted in decreased vimentin expression and cell adherence as well as increased apoptosis resistance. In cases of endometriosis and endometrial cancer, OLFM-4 expression correlated with the presence of epidermal growth factor receptor-1 and estrogen receptor-alpha (or estrogen signaling). An increase of OLFM-4 mRNA was observed in the endometrium of endometriosis patients. No change in OLFM-4 expression levels were observed in patients with endometrial cancer relative with controts. In conclusion, cross-talk between estrogen and EGF signaling regulates OLFM-4 expression. The role of OLFM-4 in endometrial tissue remodeling before the secretory phase and during the predisposition and early events in endometriosis can be postulated but requires additional investigation.}},
  author       = {{DASSEN, HELEN and Punyadeera, Chamindie and Delvoux, Bert and Schulkens, Iris and Marchetti, Claudia and Kamps, Rick and Klomp, Jan and Dijcks, Fred and de Goeij, Anton and D'Hooghe, Thomas and Kyama, Cleophas and Ederveen, Antwan and Dunselman, Gerard and Groothuis, Patrick and Romano, Andrea}},
  issn         = {{0002-9440}},
  journal      = {{AMERICAN JOURNAL OF PATHOLOGY}},
  keywords     = {{PROTEIN,RECEPTOR,CELLS,CANCER,HGC-1,KINASE,SERIAL ANALYSIS,GASTRIC-CARCINOMA,MENSTRUAL-CYCLE,GENE-EXPRESSION}},
  language     = {{eng}},
  number       = {{5}},
  pages        = {{2495--2508}},
  title        = {{Olfactomedin-4 regulation by estrogen in the human endometrium requires epidermal growth factor signaling}},
  url          = {{http://doi.org/10.2353/ajpath.2010.100026}},
  volume       = {{177}},
  year         = {{2010}},
}

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