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Journal article

Targeting Chromosomal Instability and Tumour Heterogeneity in HER2-Positive Breast Cancer

From

Cancer Research UK1

Center for Biological Sequence Analysis, Department of Systems Biology, Technical University of Denmark2

Department of Systems Biology, Technical University of Denmark3

Royal Marsden Hospital4

Breast Cancer Now Toby Robins Research Centre5

Chromosomal instability (CIN) is a common cause of tumour heterogeneity and poor prognosis in solid tumours and describes cell-cell variation in chromosome structure or number across a tumour population. In this article we consider evidence suggesting that CIN may be targeted and may influence response to distinct chemotherapy regimens, using HER2-positive breast cancer as an example.

Pre-clinical models have indicated a role for HER2 signalling in initiating CIN and defective cell-cycle control, and evidence suggests that HER2-targeting may attenuate this process. Anthracyclines and platinum agents may target tumours with distinct patterns of karyotypic complexity, whereas taxanes may have preferential activity in tumours with relative chromosomal stability.

A greater understanding of karyotypic complexity and identification of methods to directly examine and target CIN may support novel strategies to improve outcome in cancer. J. Cell. Biochem. 111: 782-790, 2010.

Language: English
Publisher: Wiley Subscription Services, Inc., A Wiley Company
Year: 2010
Pages: 782-790
ISSN: 10974644 , 07331959 and 07302312
Types: Journal article
DOI: 10.1002/jcb.22781

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