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基因表达分析鉴定出神经纤维瘤病 1 型的潜在生物标志物,包括肾上腺髓质素。

Gene expression analysis identifies potential biomarkers of neurofibromatosis type 1 including adrenomedullin.

机构信息

Division of Experimental Hematology and Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio 45229, USA.

出版信息

Clin Cancer Res. 2010 Oct 15;16(20):5048-57. doi: 10.1158/1078-0432.CCR-10-0613. Epub 2010 Aug 25.

Abstract

PURPOSE

Plexiform neurofibromas (pNF) are Schwann cell tumors found in a third of individuals with neurofibromatosis type 1 (NF1). pNF can undergo transformation to malignant peripheral nerve sheath tumors (MPNST). There are no identified serum biomarkers of pNF tumor burden or transformation to MPNST. Serum biomarkers would be useful to verify NF1 diagnosis, monitor tumor burden, and/or detect transformation.

EXPERIMENTAL DESIGN

We used microarray gene expression analysis to define 92 genes that encode putative secreted proteins in neurofibroma Schwann cells, neurofibromas, and MPNST. We validated differential expression by quantitative reverse transcription-PCR, Western blotting, and ELISA assays in cell conditioned medium and control and NF1 patient sera.

RESULTS

Of 13 candidate genes evaluated, only adrenomedullin (ADM) was confirmed as differentially expressed and elevated in serum of NF1 patients. ADM protein concentrati on was further elevated in serum of a small sampling of NF1 patients with MPNST. MPNST cell conditioned medium, containing ADM and hepatocyte growth factor, stimulated MPNST migration and endothelial cell proliferation.

CONCLUSIONS

Thus, microarray analysis identifies potential serum biomarkers for disease, and ADM is a serum biomarker of NF1. ADM serum levels do not seem to correlate with the presence of pNFs but may be a biomarker of transformation to MPNST.

摘要

目的

丛状神经纤维瘤(pNF)是神经纤维瘤病 1 型(NF1)患者中三分之一存在的雪旺氏细胞瘤。pNF 可转化为恶性外周神经鞘瘤(MPNST)。目前尚没有可识别的 pNF 肿瘤负担或转化为 MPNST 的血清生物标志物。血清生物标志物将有助于验证 NF1 诊断、监测肿瘤负担和/或检测转化。

实验设计

我们使用微阵列基因表达分析来定义 92 个基因,这些基因编码神经纤维瘤雪旺氏细胞、神经纤维瘤和 MPNST 中的推定分泌蛋白。我们通过定量逆转录-PCR、Western 印迹和 ELISA 测定在细胞条件培养基和对照及 NF1 患者血清中验证了差异表达。

结果

在评估的 13 个候选基因中,只有肾上腺髓质素(ADM)被证实为 NF1 患者血清中差异表达和升高。ADM 蛋白浓度在一小部分 NF1 伴 MPNST 患者的血清中进一步升高。MPNST 细胞条件培养基,含有 ADM 和肝细胞生长因子,刺激了 MPNST 的迁移和内皮细胞的增殖。

结论

因此,微阵列分析确定了潜在的疾病血清生物标志物,ADM 是 NF1 的血清生物标志物。ADM 血清水平似乎与 pNF 的存在无关,但可能是转化为 MPNST 的生物标志物。

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本文引用的文献

2
Evaluation of hepatocyte growth factor in patients with biliary atresia.
J Pediatr Surg. 2008 Jul;43(7):1333-7. doi: 10.1016/j.jpedsurg.2007.09.007.
5
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Horm Metab Res. 2006 Feb;38(2):112-8. doi: 10.1055/s-2006-925129.
8
Hypoxia and the hypoxia-inducible-factor pathway in glioma growth and angiogenesis.
Neuro Oncol. 2005 Apr;7(2):134-53. doi: 10.1215/S1152851704001115.
9
SPD--a web-based secreted protein database.
Nucleic Acids Res. 2005 Jan 1;33(Database issue):D169-73. doi: 10.1093/nar/gki093.
10
Hepatocyte growth factor, its receptor, and their potential value in cancer therapies.
Crit Rev Oncol Hematol. 2005 Jan;53(1):35-69. doi: 10.1016/j.critrevonc.2004.09.004.

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