Literature DB >> 11905688

Tamoxifen: a personal retrospective.

V C Jordan1.   

Abstract

Tamoxifen, originally described as an anti-oestrogen and antifertility agent in the rat, is now a pioneering medicine for the treatment and prevention of breast cancer. Its success is the result of an effective collaboration between laboratory research and clinical trial processes. However, this drug is more than just an anti-oestrogen to treat breast cancer. Laboratory and clinical research defined the concept of selective oestrogen receptor modulation in the 1980s. Non-steroidal anti-oestrogens show oestrogen-like activity in bones and lower cholesterol, but block oestrogen action in the breast and uterus. This realisation led to the development of chemical cousins, known as selective oestrogen receptor modulators. One of these compounds, raloxifene, is used for the prevention of osteoporosis, but is currently being tested as a preventive for breast cancer.

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Year:  2000        PMID: 11905688     DOI: 10.1016/S1470-2045(00)00009-7

Source DB:  PubMed          Journal:  Lancet Oncol        ISSN: 1470-2045            Impact factor:   41.316


  6 in total

Review 1.  Familiar drugs may prevent cancer.

Authors:  R A Sharma; A J Gescher; K J O'Byrne; W P Steward
Journal:  Postgrad Med J       Date:  2001-08       Impact factor: 2.401

Review 2.  International Union of Basic and Clinical Pharmacology. XCVII. G Protein-Coupled Estrogen Receptor and Its Pharmacologic Modulators.

Authors:  Eric R Prossnitz; Jeffrey B Arterburn
Journal:  Pharmacol Rev       Date:  2015-07       Impact factor: 25.468

3.  Tamoxifen induces a pluripotency signature in breast cancer cells and human tumors.

Authors:  George Notas; Vassiliki Pelekanou; Marilena Kampa; Konstantinos Alexakis; Stelios Sfakianakis; Aggelos Laliotis; John Askoxilakis; Eleftheria Tsentelierou; Maria Tzardi; Andreas Tsapis; Elias Castanas
Journal:  Mol Oncol       Date:  2015-06-05       Impact factor: 6.603

4.  TM6SF2 and MAC30, new enzyme homologs in sterol metabolism and common metabolic disease.

Authors:  Luis Sanchez-Pulido; Chris P Ponting
Journal:  Front Genet       Date:  2014-12-11       Impact factor: 4.599

5.  Molecular classification of selective oestrogen receptor modulators on the basis of gene expression profiles of breast cancer cells expressing oestrogen receptor alpha.

Authors:  A S Levenson; I L Kliakhandler; K M Svoboda; K M Pease; S A Kaiser; J E Ward; V C Jordan
Journal:  Br J Cancer       Date:  2002-08-12       Impact factor: 7.640

6.  Antitumour efficacy of VEGFR2 tyrosine kinase inhibitor correlates with expression of VEGF and its receptor VEGFR2 in tumour models.

Authors:  I K Dev; R E Dornsife; T M Hopper; J A Onori; C G Miller; L E Harrington; K M Dold; R J Mullin; J H Johnson; R M Crosby; A T Truesdale; A H Epperly; K W Hinkle; M Cheung; J A Stafford; D K Luttrell; R Kumar
Journal:  Br J Cancer       Date:  2004-10-04       Impact factor: 7.640

  6 in total

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