首页> 外国专利> METHOD FOR IDENTIFYING GENETIC MARKERS FOR SECONDARY TUMORS AND MEANS FOR THE IDENTIFICATION, LABELLING AND TARGETING OF SECONDARY TUMORS

METHOD FOR IDENTIFYING GENETIC MARKERS FOR SECONDARY TUMORS AND MEANS FOR THE IDENTIFICATION, LABELLING AND TARGETING OF SECONDARY TUMORS

机译:识别二级肿瘤遗传标记的方法以及二级肿瘤的识别,标记和靶向方法

摘要

In comparison with primary tumors, where the organ by itself is the starting point of the malignant degeneration, metastases inherit a different emergence. The molecular causes leading to secondary liver malignancies are unknown so far. The aim of the present invention is therefore to make available an easy and efficient method for identifying therapeutical targets in secondary tumors, the use of novel therapeutical targets identified by the method for screening and determiningbeneficial means and/or drugs, and means and drugs for identifying, labeling and treating secondary metastases in the liver made up of or derived from tumor cells of the colon. In principle, expression of transcription factors is studied in the primary tumor, the secondary tumor and in the healthy organ, wherein the secondary tumor is formed, according to the invention, in particular of transcription factors being enriched in the healthy tissue of the organ, wherein the secondary tumor is formed, e.g. expression of liver enriched transcription factors HNF6 and/or Foxa2 or of NGN3, HSP105B, HSP10, HNF1 ß, C/EBP is studied, such as by reverse transcription polymerase chain reaction, by gene chip analysis, by Western blotting technique, by studying the DNA binding of liver enriched transcription factors by electromobility shift assay (EMSA) or by genomic sequencing of therapeutical targets, such as of HNF6.
机译:与原发肿瘤(器官本身是恶性变性的起点)相比,转移灶继承了不同的出现方式。到目前为止,导致继发性肝恶性肿瘤的分子原因尚不清楚。因此,本发明的目的是提供一种用于鉴定继发性肿瘤中的治疗靶标的简便有效的方法,通过该方法鉴定和鉴定有益手段和/或药物的新型治疗靶标的用途,以及用于鉴定的手段和药物。 ,标记和治疗由结肠肿瘤细胞组成或源自结肠肿瘤细胞的肝脏继发转移。原则上,在原发性肿瘤,继发性肿瘤和健康器官中研究了转录因子的表达,根据本发明,其中形成了继发性肿瘤,特别是在器官的健康组织中富集了转录因子,其中继发性肿瘤形成,例如研究肝脏富集转录因子HNF6和/或Foxa2或NGN3,HSP105B,HSP10,HNF1ß,C / EBP的表达,例如通过逆转录聚合酶链反应,基因芯片分析,Western印迹技术,通过电动迁移率测定(EMSA)或通过治疗靶标(例如HNF6)的基因组测序对富含肝脏的转录因子进行DNA结合。

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