Design and synthesis of carborane-containing estrogen receptor-beta (ERβ)-selective ligands

2015 ◽  
Vol 25 (19) ◽  
pp. 4174-4178 ◽  
Author(s):  
Kiminori Ohta ◽  
Takumi Ogawa ◽  
Akifumi Oda ◽  
Asako Kaise ◽  
Yasuyuki Endo
2009 ◽  
Vol 44 (9) ◽  
pp. 3412-3424 ◽  
Author(s):  
Michael Waibel ◽  
Meri De Angelis ◽  
Fabio Stossi ◽  
Karen J. Kieser ◽  
Kathryn E. Carlson ◽  
...  

2005 ◽  
Vol 13 (23) ◽  
pp. 6529-6542 ◽  
Author(s):  
Meri De Angelis ◽  
Fabio Stossi ◽  
Michael Waibel ◽  
Benita S. Katzenellenbogen ◽  
John A. Katzenellenbogen

Author(s):  
Hubertus Jarry

AbstractIn the human female, menopause is the permanent end of fertility, defined as occurring 12 months after the last menstrual period. During peri- and postmenopausal stages, the vast majority of women experience moderate-to-severe vasomotor symptoms, such as hot flashes and night sweats, which interfere with sleep and may be severe enough to affect quality of life. The only treatment approved by national health authorities is hormone therapy with estrogen alone or in combination with a progestagen. However, this therapeutic regimen is associated with severe side effects, such as stimulation of growth of breast cancer or cardiovascular events. Thus, there is a demand for efficient and safe alternative treatments for menopausal complaints.After the discovery of estrogen receptor beta in many organs, and confirmation of its presence in the brain, many researchers raised the question of whether ERβ-specific ligands may be novel therapeutic agents for treatment of menopausal complaints with the desirable effects of estrogen but without increased risk of tumor incidence. This minireview will briefly summarize the relevance of estrogen receptor beta and its specific ligands for the treatment of menopausal symptoms with a focus on vasomotor menopausal symptoms. At present, estrogen receptor beta-selective ligands do not seem to be active in models of prevention or reversal of osteoporosis. However, data from animal experiments suggest that estrogen receptor beta-selective ligands might be safe therapeutics for the treatment of vasomotor menopausal symptoms.


2009 ◽  
Vol 44 (9) ◽  
pp. 3560-3570 ◽  
Author(s):  
Michael Waibel ◽  
Karen J. Kieser ◽  
Kathryn E. Carlson ◽  
Fabio Stossi ◽  
Benita S. Katzenellenbogen ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (3) ◽  
pp. 722
Author(s):  
Maobi Zhu ◽  
Sen Takeda ◽  
Tomohiko Iwano

Phytoestrogens are herbal polyphenolic compounds that exert various estrogen-like effects in animals and can be taken in easily from a foodstuff in daily life. The fallopian tube lumen, where transportation of the oocyte occurs, is lined with secretory cells and multi-ciliated epithelial cells. Recently, we showed that estrogen induces multi-ciliogenesis in the porcine fallopian tube epithelial cells (FTECs) through the activation of the estrogen receptor beta (ERβ) pathway and simultaneous inhibition of the Notch pathway. Thus, ingested phytoestrogens may induce FTEC ciliogenesis and thereby affect the fecundity. To address this issue, we added isoflavones (genistein, daidzein, or glycitin) and coumestan (coumestrol) to primary culture FTECs under air–liquid interface conditions and assessed the effects of each compound. All phytoestrogens except glycitin induced multi-ciliated cell differentiation, which followed Notch signal downregulation. On the contrary, the differentiation of secretory cells decreased slightly. Furthermore, genistein and daidzein had a slight effect on the proportion of proliferating cells exhibited by Ki67 expression. Ciliated-cell differentiation is inhibited by the ERβ antagonist, PHTPP. Thus, this study suggests that phytoestrogens can improve the fallopian tube epithelial sheet homeostasis by facilitating the genesis of multi-ciliated cells and this effect depends on the ERβ-mediated pathway.


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