首页> 外国专利> FUSION GENE OF KIF5B GENE AND RET GENE, AND METHOD FOR DETERMINING EFFECTIVENESS OF CANCER TREATMENT TARGETING FUSION GENE

FUSION GENE OF KIF5B GENE AND RET GENE, AND METHOD FOR DETERMINING EFFECTIVENESS OF CANCER TREATMENT TARGETING FUSION GENE

机译:KIF5B基因和RET基因的融合基因,以及确定靶向靶向融合基因的癌症疗效的方法

摘要

In order to identify a gene that can serve as an indicator for predicting the effectiveness of a drug treatment of cancer and to provide a novel method for predicting the effectiveness of a drug treatment targeting said gene, lung adenocarcinomas were subjected to whole-transcriptome sequencing. As a result, in-frame fusion transcripts between the KIF5B gene and the RET gene were identified. The KIF5B-RET gene fusions were detected in 6 out of 319 (2%) LADC specimens from Japanese individuals and 1 out of 80 (1%) LADC specimens from U.S.A. individuals. None of the seven subjects revealed known activating mutations such as EGFR, KRAS or ALK oncogenes; thus, said gene fusions were found to be responsible mutations (driver mutations) for oncogenesis. Since said gene fusions are considered to induce constitutive activation of RET tyrosine kinase protein, it was found that treatments with RET tyrosine kinase inhibitors are effective in patients with detection of said gene fusions.
机译:为了鉴定可用作预测癌症药物治疗效果的指标的基因并提供预测针对所述基因的药物治疗效果的新方法,对肺腺癌进行了全转录组测序。结果,鉴定了KIF5B基因和RET基因之间的框内融合转录物。在来自日本个人的319个(2%)LADC标本中有6个检测到了KIF5B-RET基因融合体,来自美国的80个(1%)的LADC标本中有1个检测到了KIF5B-RET基因融合体。七个受试者中没有一个发现已知的激活突变,例如EGFR,KRAS或ALK癌基因。因此,发现所述基因融合体是致癌作用的负责突变(驱动子突变)。由于所述基因融合被认为诱导RET酪氨酸激酶蛋白的组成性活化,因此发现用RET酪氨酸激酶抑制剂的治疗在检测所述基因融合的患者中是有效的。

著录项

  • 公开/公告号EP2740742A4

    专利类型

  • 公开/公告日2015-06-17

    原文格式PDF

  • 申请/专利权人 NATIONAL CANCER CENTER;LSIP LLC;

    申请/专利号EP20120820601

  • 发明设计人 KOHNO TAKASHI;TSUTA KOJI;

    申请日2012-08-03

  • 分类号C07K14/71;A61K45;A61P35;C07K14/82;C07K16/32;C12N9/12;C12N9/14;C12N15/09;

  • 国家 EP

  • 入库时间 2022-08-21 15:05:46

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