首页> 外国专利> IDENTIFICATION OF GENES INVOLVED IN ANGIOGENESIS, AND DEVELOPMENT OF AN ANGIOGENESIS DIAGNOSTIC CHIP TO IDENTIFY PATIENTS WITH IMPAIRED ANGIOGENESIS

IDENTIFICATION OF GENES INVOLVED IN ANGIOGENESIS, AND DEVELOPMENT OF AN ANGIOGENESIS DIAGNOSTIC CHIP TO IDENTIFY PATIENTS WITH IMPAIRED ANGIOGENESIS

机译:识别参与血管生成的基因,并开发血管生成诊断芯片以鉴定血管生成不良的患者

摘要

The invention is directed to methods for angiotyping individual patients to predict the likelihood of whether a given individual will develop good vs. poor collaterals naturally. Accordingly, this can involve obtaining and providing a list of genes involved in collateral development. In particular, angiotyping individual patients can be used to predict the likelihood of whether a given individual will develop good vs. poor collaterals in response to specific angiogenesis therapy. From an array of genes that have been determined through experimental studies as being differentially expressed in tissues in which collaterals are developing in response to arterial occlusion, single nucleotide polymorphisms (SNPs), or other epigenetic changes, such as DNA methylation patterns, can be identified. SNPs and DNA methylation patterns are detected using microchips or similar technology assaying for all, or most, of the genes determined to play a role in collateral development. In addition, abnormally low or abnormally high differential expression of any combination of the candidate genes can be detected in such tissue as peripheral blood cells. The presence of a predisposition to develop poor vs. good collaterals is indicated by the presence of SNPs, and/or alterations in DNA methylation patterns, and/or difference in expression levels involving one or more of the genes.
机译:本发明涉及用于对个体患者进行血管分型以预测给定个体相对于自然将发展好还是不好的侧支的可能性的方法。因此,这可能涉及获得并提供参与附带发育的基因列表。特别地,血管分型的个体患者可以用来预测给定的个体响应于特定的血管生成疗法而将发展好还是不好的侧支的可能性。从一系列通过实验研究确定为在动脉闭塞反应中产生侧支的组织中差异表达的基因中,可以鉴定出单核苷酸多态性(SNP)或其他表观遗传变化,例如DNA甲基化模式。 。使用微芯片或类似技术检测所有或大多数确定在侧支发育中起作用的基因,即可检测出SNP和DNA甲基化模式。另外,可以在诸如外周血细胞的组织中检测到候选基因的任何组合的异常低或异常高的差异表达。 SNP的存在和/或DNA甲基化模式的改变和/或涉及一种或多种基因的表达水平的差异表明,容易产生不良或良好的侧支。

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