Literature DB >> 20156170

Fulvestrant - a novel endocrine therapy for breast cancer.

S J Johnston1, K L Cheung.   

Abstract

Fulvestrant is a novel endocrine therapy for breast cancer, with a unique structure and mode of action. It binds competitively to the oestrogen receptor (ER), with high affinity, and downregulates ER by functional blockade and increased turnover. Fulvestrant has reached the clinic via extensive pre-clinical and clinical trials, which demonstrated fulvestrant's unique characteristics and showed that they translate to equivalent or improved clinical efficacy compared to established endocrine agents. Fulvestrant is currently licensed for use in postmenopausal women with hormone receptor positive advanced breast cancer which has progressed on prior endocrine therapy. As a pure oestrogen antagonist, fulvestrant avoids the risk of detrimental side effects of selective ER modulators such as tamoxifen, which has partial agonist activity. Fulvestrant, the only parenteral agent in this setting, has a good side effect profile and is well tolerated. Due to its unique mode of action, fulvestrant lacks cross-resistance with existing agents. Fulvestrant is the subject of much ongoing research, which utilises knowledge of its novel mechanism and pharmacokinetic profile in order to optimise clinical efficacy and explore new roles, including first-line use in advanced breast cancer, use in combination with existing agents, in males, and in premenopausal women, and use as an adjuvant therapy.

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Year:  2010        PMID: 20156170     DOI: 10.2174/092986710790820633

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  24 in total

Review 1.  Skeletal manifestations of treatment of breast cancer on premenopausal women.

Authors:  Loomee Doo; Charles L Shapiro
Journal:  Curr Osteoporos Rep       Date:  2013-12       Impact factor: 5.096

Review 2.  Minireview: dynamic structures of nuclear hormone receptors: new promises and challenges.

Authors:  S Stoney Simons; Dean P Edwards; Raj Kumar
Journal:  Mol Endocrinol       Date:  2013-11-27

3.  Stabilization of MORC2 by estrogen and antiestrogens through GPER1- PRKACA-CMA pathway contributes to estrogen-induced proliferation and endocrine resistance of breast cancer cells.

Authors:  Fan Yang; Hong-Yan Xie; Li-Feng Yang; Lin Zhang; Fang-Lin Zhang; Hong-Yi Liu; Da-Qiang Li; Zhi-Ming Shao
Journal:  Autophagy       Date:  2019-09-06       Impact factor: 16.016

Review 4.  Recent progress in selective estrogen receptor downregulators (SERDs) for the treatment of breast cancer.

Authors:  Irshad Ahmad; Shimy Mathew; Sofia Rahman
Journal:  RSC Med Chem       Date:  2020-03-06

Review 5.  Breast cancer: insights in disease and influence of drug methotrexate.

Authors:  Vítor Yang; Maria João Gouveia; Joana Santos; Beate Koksch; Irina Amorim; Fátima Gärtner; Nuno Vale
Journal:  RSC Med Chem       Date:  2020-05-28

6.  Epidermal growth factor and estrogen act by independent pathways to additively promote the release of the angiogenic chemokine CXCL8 by breast tumor cells.

Authors:  Karin Haim; Polina Weitzenfeld; Tsipi Meshel; Adit Ben-Baruch
Journal:  Neoplasia       Date:  2011-03       Impact factor: 5.715

7.  Potential interference of aluminum chlorohydrate with estrogen receptor signaling in breast cancer cells.

Authors:  Vyron A Gorgogietas; Ioannis Tsialtas; Natalie Sotiriou; Vasiliki C Laschou; Aikaterini G Karra; Demetres D Leonidas; George P Chrousos; Evagelia Protopapa; Anna-Maria G Psarra
Journal:  J Mol Biochem       Date:  2018

8.  Novel Selective Estrogen Receptor Ligand Conjugates Incorporating Endoxifen-Combretastatin and Cyclofenil-Combretastatin Hybrid Scaffolds: Synthesis and Biochemical Evaluation.

Authors:  Patrick M Kelly; Niall O Keely; Sandra A Bright; Bassem Yassin; Gloria Ana; Darren Fayne; Daniela M Zisterer; Mary J Meegan
Journal:  Molecules       Date:  2017-08-31       Impact factor: 4.411

9.  Tetrahydroisoquinoline Phenols: Selective Estrogen Receptor Downregulator Antagonists with Oral Bioavailability in Rat.

Authors:  James S Scott; Andrew Bailey; Robert D M Davies; Sébastien L Degorce; Philip A MacFaul; Helen Gingell; Thomas Moss; Richard A Norman; Jennifer H Pink; Alfred A Rabow; Bryan Roberts; Peter D Smith
Journal:  ACS Med Chem Lett       Date:  2015-12-19       Impact factor: 4.345

10.  The estrogen receptor fusion system in mouse models: a reversible switch.

Authors:  Jonathan Whitfield; Trevor Littlewood; Gerard I Evan; Laura Soucek
Journal:  Cold Spring Harb Protoc       Date:  2015-03-02
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