Literature DB >> 12036407

The search for the ideal SERM.

Banu Arun1, Marietta Anthony, Barbara Dunn.   

Abstract

Selective oestrogen receptor modulators (SERMs) are compounds that interact with the oestrogen receptor and have tissue-specific effects distinct from those of oestradiol, acting as an oestrogen agonist in some tissues and as an antagonist in others. The development of SERMs that selectively interact with specific receptors, coactivators and corepressors in different organ systems offers the possibility of improving the risk:benefit profile relative to hormone replacement therapy. Tamoxifen is a SERM that acts as an oestrogen antagonist in breast tissue and is currently being used for the treatment and prevention of breast cancer. Tamoxifen also exhibits oestrogen-agonistic properties in the endometrium and increases the risk of endometrial cancer. Oestrogen and another SERM, raloxifene, have been shown to prevent osteoporosis. The effects of oestrogens on cognitive functions are currently being investigated. Recent data reveal the lack of secondary prevention of coronary heart disease with oestrogen. Oestrogen has been used to treat menopausal symptoms, whereas the SERMs have been shown to induce hot flushes. Current research is focused on producing the ideal SERM, which would have benefits over existing SERMs in terms of preventing cancer, cardiovascular disease, osteoporosis and menopausal symptoms, improving cognitive functions, and have a significantly better toxicity profile in terms of endometrial cancer and thromboembolic events.

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Year:  2002        PMID: 12036407     DOI: 10.1517/14656566.3.6.681

Source DB:  PubMed          Journal:  Expert Opin Pharmacother        ISSN: 1465-6566            Impact factor:   3.889


  8 in total

1.  Efficacy and safety of bazedoxifene in postmenopausal Asian women.

Authors:  L Xu; K-S Tsai; G S Kim; Y Wu; P Vincendon; A A Chines; G D Constantine
Journal:  Osteoporos Int       Date:  2010-06-10       Impact factor: 4.507

2.  Safety and tolerability of bazedoxifene in postmenopausal women with osteoporosis: results of a 5-year, randomized, placebo-controlled phase 3 trial.

Authors:  T J de Villiers; A A Chines; S Palacios; P Lips; A Z Sawicki; A B Levine; C Codreanu; N Kelepouris; J P Brown
Journal:  Osteoporos Int       Date:  2010-06-10       Impact factor: 4.507

3.  DT56a stimulates creatine kinase specific activity in vascular tissues of rats.

Authors:  D Somjen; I Yoles
Journal:  J Endocrinol Invest       Date:  2003-10       Impact factor: 4.256

Review 4.  Tamoxifen regulation of sphingolipid metabolism--Therapeutic implications.

Authors:  Samy A F Morad; Myles C Cabot
Journal:  Biochim Biophys Acta       Date:  2015-05-09

Review 5.  Individualizing osteoporosis therapy.

Authors:  S Silverman; C Christiansen
Journal:  Osteoporos Int       Date:  2012-01-05       Impact factor: 4.507

6.  Safety of bazedoxifene in a randomized, double-blind, placebo- and active-controlled Phase 3 study of postmenopausal women with osteoporosis.

Authors:  Claus Christiansen; Charles H Chesnut; Jonathan D Adachi; Jacques P Brown; César E Fernandes; Annie Wc Kung; Santiago Palacios; Amy B Levine; Arkadi A Chines; Ginger D Constantine
Journal:  BMC Musculoskelet Disord       Date:  2010-06-22       Impact factor: 2.362

7.  Cost-effectiveness of bazedoxifene versus raloxifene in the treatment of postmenopausal women in Spain.

Authors:  Josep Darbà; Nuria Pérez-Álvarez; Lisette Kaskens; Susana Holgado-Pérez; Jill Racketa; Javier Rejas
Journal:  Clinicoecon Outcomes Res       Date:  2013-07-05

Review 8.  Fulvestrant: an oestrogen receptor antagonist with a novel mechanism of action.

Authors:  C K Osborne; A Wakeling; R I Nicholson
Journal:  Br J Cancer       Date:  2004-03       Impact factor: 7.640

  8 in total

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