Literature DB >> 17591833

Overview and new strategies in metastatic breast cancer (MBC) for treatment of tamoxifen-resistant patients.

V Adamo1, M Iorfida, E Montalto, V Festa, C Garipoli, A Scimone, M Zanghì, N Caristi.   

Abstract

The treatment with aromatase inhibitors (AIs) and fulvestrant has been demonstrated to be active in a proportion of tamoxifen-resistant breast cancer patients, obtaining, in some cases, a long-term control of tumor growth. Results from clinical trials indicate that treatment with fulvestrant might either precede or follow AIs. However, the AIs are now replacing tamoxifen as first-line advanced and adjuvant therapies, and thus, other options following tamoxifen failure are required. Fulvestrant may be effective in this setting, even if there is also evidence of a lack of cross-resistance between nonsteroidal and steroidal AIs, resulting in the potential use of steroidal AIs following nonsteroidal AI failure and vice versa. Resistance mechanisms to these therapies appear to be related to a cross talk between estrogen receptor (ER) and growth factor-signaling cascades. Novel therapeutic approaches for ER+ patients, which combine hormonal agents and signal transduction inhibitors, have been developed to overcoming resistance. Several trials are now investigating signal transduction inhibitors combined with endocrine agents. This approach might provide efficient treatments and delay the onset of antihormone resistance, thereby significantly improving patient's survival.

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Year:  2007        PMID: 17591833     DOI: 10.1093/annonc/mdm225

Source DB:  PubMed          Journal:  Ann Oncol        ISSN: 0923-7534            Impact factor:   32.976


  7 in total

1.  Med1 plays a critical role in the development of tamoxifen resistance.

Authors:  Arumugam Nagalingam; Mourad Tighiouart; Lisa Ryden; Leena Joseph; Goran Landberg; Neeraj K Saxena; Dipali Sharma
Journal:  Carcinogenesis       Date:  2012-02-16       Impact factor: 4.944

2.  Computational investigation of the binding mode of bis(hydroxylphenyl)arenes in 17β-HSD1: molecular dynamics simulations, MM-PBSA free energy calculations, and molecular electrostatic potential maps.

Authors:  Matthias Negri; Maurizio Recanatini; Rolf W Hartmann
Journal:  J Comput Aided Mol Des       Date:  2011-08-06       Impact factor: 3.686

3.  Prolylcarboxypeptidase regulates proliferation, autophagy, and resistance to 4-hydroxytamoxifen-induced cytotoxicity in estrogen receptor-positive breast cancer cells.

Authors:  Lei Duan; Natalia Motchoulski; Brian Danzer; Irina Davidovich; Zia Shariat-Madar; Victor V Levenson
Journal:  J Biol Chem       Date:  2010-11-17       Impact factor: 5.157

4.  Effects of celecoxib and ly117018 combination on human breast cancer cells in vitro.

Authors:  Klaus H Baumann; Elmar Klusmeier; Isabel Eggemann; Silke Reinartz; Achim Almeroth; Mathias Kalder; Uwe Wagner
Journal:  Breast Cancer (Auckl)       Date:  2009-04-07

5.  Combined histone deacetylase inhibition and tamoxifen induces apoptosis in tamoxifen-resistant breast cancer models, by reversing Bcl-2 overexpression.

Authors:  Paromita Raha; Scott Thomas; K Ted Thurn; Jeenah Park; Pamela N Munster
Journal:  Breast Cancer Res       Date:  2015-02-25       Impact factor: 6.466

6.  Silencing of keratinocyte growth factor receptor restores 5-fluorouracil and tamoxifen efficacy on responsive cancer cells.

Authors:  Sabrina Rotolo; Simona Ceccarelli; Ferdinando Romano; Luigi Frati; Cinzia Marchese; Antonio Angeloni
Journal:  PLoS One       Date:  2008-06-25       Impact factor: 3.240

7.  The Effect of Selective Estrogen Receptor Modulators (SERMs) on the Tamoxifen Resistant Breast Cancer Cells.

Authors:  Bo Yoon Chang; Sae Am Kim; Bindu Malla; Sung Yeon Kim
Journal:  Toxicol Res       Date:  2011-06
  7 in total

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