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Comprehensive molecular portraits of human breast tumours

A. McCullough
- 01 Jan 2013 - 
- Vol. 2013, pp 286-288
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This article is published in Yearbook of Pathology and Laboratory Medicine.The article was published on 2013-01-01. It has received 5867 citations till now.

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Harnessing the potential of epigenetic therapy to target solid tumors.

TL;DR: It is suggested that current drugs may represent a targeted therapeutic approach for reprogramming solid tumor cells, a strategy that must be pursued in concert with the explosion in knowledge about the molecular underpinnings of normal and cancer epigenomes.
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Triple-negative breast cancer: the importance of molecular and histologic subtyping, and recognition of low-grade variants.

TL;DR: The heterogeneity of TNBC is described and a family of low-grade triple-negative lesions that, despite having low- grade morphology and indolent clinical behavior, have been shown to harbor the complex genomic landscape of common forms of T NBC, and may progress to high-grade disease.
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Aromatase expression and regulation in breast and endometrial cancer

TL;DR: Targeting these distinct pathways and/or transcription factors to modify aromatase activity may lead to the development of novel therapeutic remedies that inhibit estrogen production in a tissue-specific manner.
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Digital image analysis outperforms manual biomarker assessment in breast cancer

TL;DR: DIA outperformed manual scoring in terms of sensitivity and specificity for the Luminal B subtype, widely considered the most challenging distinction in surrogate subclassification, and produced slightly better concordance and Cohen’s κ agreement with PAM50 gene expression assays.
References
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Journal ArticleDOI

Comprehensive molecular portraits of human breast tumours

Daniel C. Koboldt, +355 more
- 04 Oct 2012 - 
TL;DR: The ability to integrate information across platforms provided key insights into previously defined gene expression subtypes and demonstrated the existence of four main breast cancer classes when combining data from five platforms, each of which shows significant molecular heterogeneity.