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Open AccessJournal ArticleDOI

Multidrug Resistance in Breast Cancer: From In Vitro Models to Clinical Studies

N.S. Wind, +1 more
- 24 Feb 2011 - 
- Vol. 2011, pp 967419-967419
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TLDR
Evidence of the potential roles of key molecules associated with breast cancer MDR are summarized and possible explanations for why despite several decades of research, the precise role of ABC transporters remains elusive are provided.
Abstract
The development of multidrug resistance (MDR) and subsequent relapse on therapy is a widespread problem in breast cancer, but our understanding of the underlying molecular mechanisms is incomplete. Numerous studies have aimed to establish the role of drug transporter pumps in MDR and to link their expression to response to chemotherapy. The ATP-binding cassette (ABC) transporters are central to breast cancer MDR, and increases in ABC expression levels have been shown to correlate with decreases in response to various chemotherapy drugs and a reduction in overall survival. But as there is a large degree of redundancy between different ABC transporters, this correlation has not been seen in all studies. This paper provides an introduction to the key molecules associated with breast cancer MDR and summarises evidence of their potential roles reported from model systems and clinical studies. We provide possible explanations for why despite several decades of research, the precise role of ABC transporters in breast cancer MDR remains elusive.

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Citations
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Classification, Treatment Strategy, and Associated Drug Resistance in Breast Cancer

TL;DR: It is believed that the understanding of the molecular mechanisms of each treatment and subsequent drug resistance development will eventually lead to the discovery of more effective and efficient second-line therapeutics.
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Emerging roles of extracellular vesicles in the adaptive response of tumour cells to microenvironmental stress.

TL;DR: Some of the major phenotypic characteristics of the hostile tumour microenvironment and the emerging roles of extracellular vesicles in these events are reviewed.
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MiR-222 and miR-29a contribute to the drug-resistance of breast cancer cells.

TL;DR: This study demonstrates that altered miRNA expression pattern is involved in acquiring resistance to Adr and Doc in breast cancer MCF-7 cells, and that there are some miRNAs who displayed consistent up- or down-regulated expression changes in the two resistant sublines.
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Nanomedicine applications in the treatment of breast cancer: current state of the art.

TL;DR: An overview of the current breast cancer treatment and the updated status of nanomedicine use in clinical setting is given, then the latest important trends in designing breast cancer nanomedICine are discussed, including passive and active cancer cell targeting, breast cancer stem celltargeting, tumor microenvironment-based nanotherapy and combination nanotherapy of drug-resistant breast cancer.
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The Evolution and Ecology of Resistance in Cancer Therapy

TL;DR: This approach has shown that, although emergence of resistance mechanisms in cancer cells to every current therapy is inevitable, proliferation of the resistant phenotypes is not and can be delayed and even prevented with sufficient understanding of the underlying ecoevolutionary dynamics.
References
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TL;DR: It is demonstrated that an oncogene, specifically the adenovirus E1A gene, can sensitize fibroblasts to apoptosis induced by ionizing radiation, 5-fluorouracil, etoposide, and adriamycin, and the involvement of p53 in the apoptotic response suggests a mechanism whereby tumor cells can acquire cross-resistance to anticancer agents.
Journal ArticleDOI

Isolation and functional properties of murine hematopoietic stem cells that are replicating in vivo.

TL;DR: It is discovered that display of Hoechst fluorescence simultaneously at two emission wavelengths revealed a small and distinct subset of whole bone marrow cells that had phenotypic markers of multipotential HSC, which were shown in competitive repopulation experiments to contain the vast majority of HSC activity from murine bone marrow and to be enriched at least 1,000-fold for in vivo reconstitution activity.
Journal ArticleDOI

The human ATP-binding cassette (ABC) transporter superfamily

TL;DR: The ATP-binding cassette (ABC) transporters are essential for many processes in the cell and mutations in these genes cause or contribute to several human genetic disorders including cystic fibrosis, neurological disease, retinal degeneration, cholesterol and bile transport defects, anemia, and drug response.
Journal ArticleDOI

Biochemical, cellular, and pharmacological aspects of the multidrug transporter

TL;DR: This review summarizes current research on the structure-function analysis of P-glycoprotein, its mechanism of action, and facts and speculations about its normal physiological role.
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