共 22 条
Gene expression profiling of human dermal fibroblasts exposed to bleomycin sulphate does not differentiate between radiation sensitive and control patients
被引:5
|作者:
Westbury, Charlotte B.
[1
,2
,3
]
Sahlberg, Kristine Kleivi
[4
]
Borresen-Dale, Anne-Lise
[4
,5
]
Isacke, Clare M.
[1
]
Yarnold, John R.
[2
,3
]
机构:
[1] Inst Canc Res, Breakthrough Breast Canc Res Ctr, London SW3 6JB, England
[2] Royal Marsden NHS Fdn Trust, Dept Radiotherapy, Sutton SM2 5PT, Surrey, England
[3] Inst Canc Res, Sutton SM2 5PT, Surrey, England
[4] Norwegian Radium Hosp, Inst Canc Res, Dept Genet, N-0310 Oslo, Norway
[5] Univ Oslo, Inst Clin Med, N-0316 Oslo, Norway
来源:
关键词:
EARLY BREAST-CANCER;
IONIZING-RADIATION;
RADIOTHERAPY;
FIBROSIS;
CHECKPOINT;
RISK;
SKIN;
D O I:
10.1186/1748-717X-6-42
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Background: Gene expression profiling of the transcriptional response of human dermal fibroblasts to in vitro radiation has shown promise as a predictive test of radiosensitivity. This study tested if treatment with the radiomimetic drug bleomycin sulphate could be used to differentiate radiation sensitive patients and controls in patients who had previously received radiotherapy for early breast cancer. Findings: Eight patients who developed marked late radiation change assessed by photographic breast appearance and 8 matched patients without any change were selected from women entered in a prospective randomised trial of breast radiotherapy fractionation. Gene expression profiling of primary skin fibroblasts exposed in vitro to bleomycin sulphate and mock treated fibroblast controls was performed. 973 genes were up-regulated and 923 down-reguated in bleomycin sulphate treated compared to mock treated control fibroblasts. Gene ontology analysis revealed enriched groups were cellular localisation, apoptosis, cell cycle and DNA damage response for the deregulated genes. No transcriptional differences were identified between fibroblasts from radiation sensitive cases and control patients; subgroup analysis using cases exhibiting severe radiation sensitivity or with high risk alleles present in TGF beta 1 also showed no difference. Conclusions: The transcriptional response of human dermal fibroblasts to bleomycin sulphate has been characterised. No differences between clinically radiation sensitive and control patients were detected using this approach.
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