4.7 Article

High bone marrow angiopoietin-1 expression is an independent poor prognostic factor for survival in patients with myelodysplastic syndromes

期刊

BRITISH JOURNAL OF CANCER
卷 105, 期 7, 页码 975-982

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/bjc.2011.340

关键词

angiopoietin; vascular endothelial growth factor; myelodysplastic syndromes; prognosis

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资金

  1. National Science Council (Taiwan) [NSC 97-2314-B002-015-MY3, NSC-97-2628-B-002-002-MY3]
  2. Department of Health (Taiwan) [DOH99-TD-C-111-001]
  3. Department of Medical Research, National Taiwan University Hospital [NTUH.99P14]

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BACKGROUND: Angiogenic factors have an essential role in normal and pathologic angiogenesis. However, the clinical implication of angiogenic factor expression in myelodysplastic syndromes (MDS) remains unclear. METHODS: In this study, we sought to investigate the prognostic impact of the expression of genes encoding angiopoietin-1 (Ang-1), Ang-2, the receptor Tie2, vascular endothelial growth factor-A (VEGF-A) and VEGF-C in the bone marrow (BM) in 208 patients with newly diagnosed primary MDS. RESULTS: BM Ang-1 expression was significantly higher in MDS patients, especially those with higher-risk subtypes, than in normal controls. With a median follow-up time of 32.9 months, the disease transformed to acute leukaemia more frequently in the patients bearing higher Ang-1 expression than in those with lower expression (31.5% vs 18.6%, P = 0.023). The MDS patients with higher Ang-1 expression had shorter overall survival than those with lower expression (median 20.8 +/- 4.5 months vs 63.3 +/- 17.8 months, P<0.001). Multivariate analyses showed that higher Ang-1 expression was an independent unfavourable prognostic factor for overall survival. There was no impact of the expression of other angiogenic factors on survival. CONCLUSION: BM Ang-1 expression may serve as a new biomarker to predict clinical outcome in MDS patients. British Journal of Cancer (2011) 105, 975-982. doi:10.1038/bjc.2011.340 www.bjcancer.com Published online 30 August 2011 (C) 2011 Cancer Research UK

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