Literature DB >> 16113086

Consensus statement. Workshop on therapeutic resistance in breast cancer: impact of growth factor signalling pathways and implications for future treatment.

J M W Gee, A Howell, W J Gullick, C C Benz, R L Sutherland, R J Santen, L-A Martin, F Ciardiello, W R Miller, M Dowsett, P Barrett-Lee, J F R Robertson, S R Johnston, H E Jones, A E Wakeling, R Duncan, R I Nicholson.   

Abstract

Anti-hormones (notably tamoxifen), chemotherapy and modern radiotherapeutic approaches are invaluable in the management of breast cancer, and collectively have contributed substantially to the improved survival in this disease. Moreover, there is promise that these successes will continue with the emergence of other endocrine agents (for example, aromatase inhibitors and pure anti-oestrogens). However, de novo and acquired resistance comprises a significant problem with all treatment approaches examined to date. This Workshop aimed to evaluate the contribution made by growth factor signalling pathways in the various resistant states, primarily focusing on resistance to anti-hormonal strategies and spanning experimental models and, where possible, clinical breast cancer data. The successes and limitations of therapeutic targeting of these pathways with various signal transduction inhibitors (STIs) were evaluated in model systems and from emerging clinical trials (including epidermal growth factor receptor inhibitors such as gefitinib). It was concluded that growth factor signalling is an important contributor in the development of endocrine resistance in breast cancer and that use of STIs provides a promising therapeutic strategy for this disease. However, the cancer cell is clearly able to harness alternative growth factor signalling pathways for growth and cell survival in the presence of STI monotherapy and, as a consequence, the efficacy of STIs is likely to be limited by the acquisition of resistance. A number of strategies were proposed from studies in model systems that appeared to enhance anti-tumour actions of existing STI monotherapy, notably including combination therapies targeting multiple pathways. With the increased availability of diverse STIs and improved drug delivery, there is much hope that the more complex therapeutic strategies proposed may ultimately be achievable in clinical practice.

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Year:  2005        PMID: 16113086     DOI: 10.1677/erc.1.01054

Source DB:  PubMed          Journal:  Endocr Relat Cancer        ISSN: 1351-0088            Impact factor:   5.678


  12 in total

1.  Dual IGF-1R/InsR inhibitor BMS-754807 synergizes with hormonal agents in treatment of estrogen-dependent breast cancer.

Authors:  Xiaonan Hou; Fei Huang; Luciana F Macedo; Sean C Harrington; Karen A Reeves; Ann Greer; Friedrich Graf Finckenstein; Angela Brodie; Marco M Gottardis; Joan M Carboni; Paul Haluska
Journal:  Cancer Res       Date:  2011-10-31       Impact factor: 12.701

2.  The adaptor protein AMOT promotes the proliferation of mammary epithelial cells via the prolonged activation of the extracellular signal-regulated kinases.

Authors:  William P Ranahan; Zhang Han; Whitney Smith-Kinnaman; Sarah C Nabinger; Brigitte Heller; Britney-Shea Herbert; Rebecca Chan; Clark D Wells
Journal:  Cancer Res       Date:  2011-02-01       Impact factor: 12.701

Review 3.  MEK5/ERK5 pathway: the first fifteen years.

Authors:  Barbara A Drew; Matthew E Burow; Barbara S Beckman
Journal:  Biochim Biophys Acta       Date:  2011-10-13

4.  Cross-talk between HER2 and MED1 regulates tamoxifen resistance of human breast cancer cells.

Authors:  Jiajun Cui; Katherine Germer; Tianying Wu; Jiang Wang; Jia Luo; Shao-chun Wang; Qianben Wang; Xiaoting Zhang
Journal:  Cancer Res       Date:  2012-09-10       Impact factor: 12.701

5.  Tumor escape in a Wnt1-dependent mouse breast cancer model is enabled by p19Arf/p53 pathway lesions but not p16 Ink4a loss.

Authors:  Michael T Debies; Shelley A Gestl; Jessica L Mathers; Oliver R Mikse; Travis L Leonard; Susan E Moody; Lewis A Chodosh; Robert D Cardiff; Edward J Gunther
Journal:  J Clin Invest       Date:  2008-01       Impact factor: 14.808

6.  Enhanced NF kappa B and AP-1 transcriptional activity associated with antiestrogen resistant breast cancer.

Authors:  Yamei Zhou; Christina Yau; Joe W Gray; Karen Chew; Shanaz H Dairkee; Dan H Moore; Urs Eppenberger; Serenella Eppenberger-Castori; Christopher C Benz
Journal:  BMC Cancer       Date:  2007-04-03       Impact factor: 4.430

7.  Accelerated blood clearance phenomenon upon cross-administration of PEGylated nanocarriers in beagle dogs.

Authors:  Chunling Wang; Xiaobo Cheng; Yuqing Su; Ying Pei; Yanzhi Song; Jiao Jiao; Zhenjun Huang; Yanfei Ma; Yinming Dong; Ying Yao; Jingjing Fan; Han Ta; Xinrong Liu; Hui Xu; Yihui Deng
Journal:  Int J Nanomedicine       Date:  2015-05-14

Review 8.  Key signalling nodes in mammary gland development and cancer. Mitogen-activated protein kinase signalling in experimental models of breast cancer progression and in mammary gland development.

Authors:  Jacqueline Whyte; Orla Bergin; Alessandro Bianchi; Sara McNally; Finian Martin
Journal:  Breast Cancer Res       Date:  2009       Impact factor: 6.466

9.  Overexpression of CD44 accompanies acquired tamoxifen resistance in MCF7 cells and augments their sensitivity to the stromal factors, heregulin and hyaluronan.

Authors:  Stephen Hiscox; Bedanta Baruha; Chris Smith; Rebecca Bellerby; Lindy Goddard; Nicola Jordan; Zaruhi Poghosyan; Robert I Nicholson; Peter Barrett-Lee; Julia Gee
Journal:  BMC Cancer       Date:  2012-10-06       Impact factor: 4.430

10.  Use of Nanotechnology to Develop Multi-Drug Inhibitors For Cancer Therapy.

Authors:  Raghavendra Gowda; Nathan R Jones; Shubhadeep Banerjee; Gavin P Robertson
Journal:  J Nanomed Nanotechnol       Date:  2013-12
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