共 86 条
Targeting Chromosomal Instability and Tumour Heterogeneity in HER2-Positive Breast Cancer
被引:44
作者:
Burrell, Rebecca A.
[1
]
Juul, Nicolai
[2
]
Johnston, Stephen R.
[3
]
Reis-Filho, Jorge S.
[4
]
Szallasi, Zoltan
[2
,5
]
Swanton, Charles
[1
,3
]
机构:
[1] London Res Inst, Translat Canc Therapeut Lab, London WC2A 3PX, England
[2] Tech Univ Denmark, Ctr Biol Sequence Anal, DK-2800 Lyngby, Denmark
[3] Royal Marsden Hosp, Breast Unit, Dept Med, Sutton SM2 5PT, Surrey, England
[4] Inst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
[5] Harvard Univ, Sch Med, Harvard Mit Div Hlth Sci & Technol CHIP HST, Childrens Hosp Informat Program, Boston, MA 02115 USA
关键词:
CHROMOSOMAL INSTABILITY;
HER2;
BREAST CANCER;
DRUG RESISTANCE;
TUMOUR HETEROGENEITY;
MICROTUBULE;
CEP17;
SPINDLE ASSEMBLY CHECKPOINT;
TAXOL-INDUCED APOPTOSIS;
IN-SITU HYBRIDIZATION;
PHASE-II TRIAL;
MITOTIC CHECKPOINT;
1ST-LINE TREATMENT;
INTRATUMORAL HETEROGENEITY;
RETROSPECTIVE ANALYSIS;
KARYOTYPIC COMPLEXITY;
ADJUVANT CHEMOTHERAPY;
D O I:
10.1002/jcb.22781
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
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. (C) 2010 Wiley-Liss, Inc.
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页码:782 / 790
页数:9
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