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本文引用的文献

1
A molecular function map of Ewing's sarcoma.尤因肉瘤的分子功能图谱。
PLoS One. 2009;4(4):e5415. doi: 10.1371/journal.pone.0005415. Epub 2009 Apr 30.
2
Overcoming resistance to conventional drugs in Ewing sarcoma and identification of molecular predictors of outcome.克服尤因肉瘤对传统药物的耐药性并确定预后的分子预测指标。
J Clin Oncol. 2009 May 1;27(13):2209-16. doi: 10.1200/JCO.2008.19.2542. Epub 2009 Mar 23.
3
The oncogenic EWS-FLI1 protein binds in vivo GGAA microsatellite sequences with potential transcriptional activation function.致癌性EWS-FLI1蛋白在体内与具有潜在转录激活功能的GGAA微卫星序列结合。
PLoS One. 2009;4(3):e4932. doi: 10.1371/journal.pone.0004932. Epub 2009 Mar 23.
4
EZH2 is a mediator of EWS/FLI1 driven tumor growth and metastasis blocking endothelial and neuro-ectodermal differentiation.EZH2是EWS/FLI1驱动的肿瘤生长和转移的介质,可阻断内皮细胞和神经外胚层分化。
Proc Natl Acad Sci U S A. 2009 Mar 31;106(13):5324-9. doi: 10.1073/pnas.0810759106. Epub 2009 Mar 16.
5
ArrayExpress update--from an archive of functional genomics experiments to the atlas of gene expression.ArrayExpress更新——从功能基因组学实验存档到基因表达图谱
Nucleic Acids Res. 2009 Jan;37(Database issue):D868-72. doi: 10.1093/nar/gkn889. Epub 2008 Nov 10.
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Lysophosphatidic acid induces cell migration through the selective activation of Akt1.溶血磷脂酸通过选择性激活Akt1诱导细胞迁移。
Exp Mol Med. 2008 Aug 31;40(4):445-52. doi: 10.3858/emm.2008.40.4.445.
7
In vitro genetic screen identifies a cooperative role for LPA signaling and c-Myc in cell transformation.体外遗传筛选确定了溶血磷脂酸(LPA)信号传导和c-Myc在细胞转化中的协同作用。
Oncogene. 2008 Nov 20;27(54):6806-16. doi: 10.1038/onc.2008.294. Epub 2008 Sep 1.
8
Identification of low intratumoral gene expression heterogeneity in neuroblastic tumors by genome-wide expression analysis and game theory.通过全基因组表达分析和博弈论鉴定神经母细胞瘤中低肿瘤内基因表达异质性
Cancer. 2008 Sep 15;113(6):1412-22. doi: 10.1002/cncr.23720.
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Molecular characterization of the pediatric preclinical testing panel.儿科临床前测试小组的分子特征分析。
Clin Cancer Res. 2008 Jul 15;14(14):4572-83. doi: 10.1158/1078-0432.CCR-07-5090.
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Horizontal gene transfer in eukaryotic evolution.真核生物进化中的水平基因转移
Nat Rev Genet. 2008 Aug;9(8):605-18. doi: 10.1038/nrg2386.

ABHD6 在尤文氏瘤中高表达。

High expression of the evolutionarily conserved alpha/beta hydrolase domain containing 6 (ABHD6) in Ewing tumors.

机构信息

Children's Cancer Research Center, Martin-Luther-University Halle-Wittenberg, University Clinic and Polyclinic for Child and Adolescent Medicine, Halle, Germany.

出版信息

Cancer Sci. 2009 Dec;100(12):2383-9. doi: 10.1111/j.1349-7006.2009.01347.x. Epub 2009 Sep 4.

DOI:10.1111/j.1349-7006.2009.01347.x
PMID:19793082
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11158961/
Abstract

Despite improvements in the treatment of patients with Ewing family tumors (EFT), the prognosis for patients with advanced disease is still unsatisfactory. Recently, we identified lipase I as an EFT-associated gene that might be interesting for the development of new immunological or pharmacological treatment strategies. Lipase I is a member of the large protein superfamilies of alpha/beta hydrolases and serine hydrolases. In the present paper we describe high expression of another member of these superfamilies in EFT. By DNA microarray data base mining we found exceptional high expression of alpha/beta hydrolase domain containing 6 (ABHD6) in EFT but not in other sarcomas. Expression of ABHD6 in EFT correlated with expression of another EFT-associated gene, aristaless. Analysis of ABHD6-associated GGAA microsatellites revealed shorter microsatellites in EFT with lack of ABHD6 expression. ABHD6 homologues were found in varying chordata but not in other animal species. Based on homology modeling we predicted the 3D-structure of ABHD6, which shows high similarity with bacterial homoserine transacetylases. High expression of ABHD6 in EFT in comparison to normal tissues and other tumors suggests that ABHD6 might be an interesting new diagnostic or therapeutic target for EFT. However, knock down of ABHD6 in EFT cells did not inhibit tumor cell growth.

摘要

尽管在治疗尤文氏家族肿瘤(EFT)患者方面取得了进展,但晚期疾病患者的预后仍然不尽如人意。最近,我们发现脂肪酶 I 是一种与 EFT 相关的基因,可能对开发新的免疫或药理学治疗策略很有意义。脂肪酶 I 是大型α/β水解酶和丝氨酸水解酶蛋白超家族的成员。在本文中,我们描述了这些超家族的另一个成员在 EFT 中的高表达。通过 DNA 微阵列数据库挖掘,我们发现 ABHD6 在 EFT 中表达异常高,而在其他肉瘤中则没有。ABHD6 在 EFT 中的表达与另一个与 EFT 相关的基因 aristaless 的表达相关。对 ABHD6 相关的 GGAA 微卫星的分析显示,在缺乏 ABHD6 表达的 EFT 中存在较短的微卫星。在不同的脊索动物中发现了 ABHD6 同源物,但在其他动物物种中则没有。基于同源建模,我们预测了 ABHD6 的 3D 结构,它与细菌高丝氨酸转乙酰酶具有高度相似性。ABHD6 在 EFT 中的高表达与正常组织和其他肿瘤相比,表明 ABHD6 可能是 EFT 的一个有趣的新诊断或治疗靶点。然而,ABHD6 在 EFT 细胞中的敲低并没有抑制肿瘤细胞的生长。