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Method for determining a chemotherapeutic regimen based on ERCC1 and TS expression

机译:基于ERCC1和TS表达的化疗方案确定方法

摘要

A method for determining a chemotherapeutic regimen comprising 5-fluorouracil which, oxaliplatin or unacombinación thereof for treating a tumor in a patient comprising: (a) fixing a tumor sample and embedding the fixed sample in paraffin; (B) isolating mRNA from the tumor sample fixed paraffin embedded by heating the detejido sample in a solution comprising an effective concentration of a chaotropic compound to a temperature inthe range of about 75 to about 100C for a period of time aproximadamentea about 120 minutes of recovering said mRNA from said chaotropic solution; (C) subjecting the mRNA to amplification using a pair of oligonucleotide primers that hybridize condicionesrigurosas to a region of the ERCC1 gene and comprises SEQ ID NO: 1 or an identical oligonucleotide primer at least 80% thereto, and SEQ ID NO: NO 2 or an oligonucleotide primer identical to at least 80% thereto, and unpar of oligonucleotide primers hidridan under stringent conditions to a region of the TS gene conditions and comprises laSEQ ID: 3 or an oligonucleotide primer identical to at least 80% thereto, and SEQ ID NO: 4 or an identical cebadoroligonucleotídico at least 80% thereto, to obtain an amplified sample of ERCC1 and TS unamuestra amplified; (D) determining the amount of TS and ERCC1 mRNA in the amplified sample; (E) comparing the amount of TS and ERCC1 mRNA from step (d) to an amount of mRNA of a gene controlinterno; and (f) determining a chemotherapeutic regimen comprising 5-fluorouracil, oxaliplatin, or combination losmismos, based on the amount of TS mRNA and / or ERCC1 in the amplified sample and the threshold level for laexpresión the TS gene and / or ERCC1.
机译:一种用于确定包含5-氟尿嘧啶,奥沙利铂或其非组合药物以治疗患者肿瘤的化疗方案的方法,该方法包括:(a)固定肿瘤样品并将固定的样品包埋在石蜡中; (B)通过将detejido样品在包含有效浓度的离液序列高的化合物的溶液中加热到约75至约100℃的温度并在大约120分钟的时间里分离前的时间,从肿瘤样品固定的石蜡中分离mRNA。来自所述离液溶液的所述mRNA; (C)使用一对使锥毛藻与ERCC1基因的区域杂交的寡核苷酸引物对mRNA进行扩增,该寡核苷酸引物包含SEQ ID NO:1或至少80%的相同寡核苷酸引物,以及SEQ ID NO:NO 2或至少与80%相同的寡核苷酸引物,以及在严格条件下不与TS基因条件区域相同的寡核苷酸引物hidridan,并包含laSEQ ID:3或与其至少80%相同的寡核苷酸引物,以及SEQ ID NO :4个或至少80%的相同的cebadoroligonucleotídico,以获得ERCC1和TS unamuestra扩增的扩增样品; (D)确定扩增样品中TS和ERCC1mRNA的量; (E)比较来自步骤(d)的TS和ERCC1 mRNA的量与基因controlinterno的mRNA的量; (f)基于扩增样品中TS mRNA和/或ERCC1的量以及表达TS基因和/或ERCC1的阈值水平,确定包含5-氟尿嘧啶,奥沙利铂或组合losmismos的化疗方案。

著录项

  • 公开/公告号ES2422302T3

    专利类型

  • 公开/公告日2013-09-10

    原文格式PDF

  • 申请/专利权人 RESPONSE GENETICS INC.;

    申请/专利号ES20010994073T

  • 发明设计人 DANENBERG KATHLEEN;

    申请日2001-11-09

  • 分类号C12N15/09;C12Q1/68;A61K31/282;A61K31/513;A61P35/00;A61P43/00;C12P19/34;C12Qnull/null;G01N33/50;G01N33/574;

  • 国家 ES

  • 入库时间 2022-08-21 16:38:35

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