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公开(公告)号:WO2017132749A1
公开(公告)日:2017-08-10
申请号:PCT/CA2017/000025
申请日:2017-02-06
Applicant: UNIVERSITY HEALTH NETWORK
Inventor: WANG, Jean , DICK, John , NG, Stanley , MINDEN, Mark , MITCHELL, Amanda , CHEN, Weihsu, Claire , ZANDSTRA, Peter , KENNEDY, James
CPC classification number: G01N33/57426 , C12Q1/6883 , C12Q2600/106 , C12Q2600/118 , C12Q2600/158 , C40B40/06 , C40B40/08 , G01N2800/52 , G06F19/10 , G06F19/20
Abstract: There is described herein a method of prognosing or classifying a subject with acute myeloid leukemia (AML) comprising: (a) determining the expression level of at least 3 genes in a test sample from the subject selected from the group consisting of DNMT3B, ZBTB46, NYNRIN, ARHGAP22, LAPTM4B, MMRN1, DPYSL3, KIAAQ125. CDK6, CPXM1, SOCS2, SMIM24, EMP1, NGFRAP1, CD34, AKR1C3, GPR56; and (b) comparing expression of the at least 3 genes in the test sample with reference expression levels of the at least 3 genes from control samples from a cohort of patients; wherein a difference or similarity in the expression of the at least 3 genes in the test sample and the reference expression levels is used to prognose or classify the subject with AML into a low risk group or a high risk group for worse survival.
Abstract translation: 本文描述了预测或分类患有急性骨髓性白血病(AML)的受试者的方法,其包括:(a)确定来自选自以下的对象的测试样品中的至少3个基因的表达水平: 由DNMT3B,ZBTB46,NYNRIN,ARHGAP22,LAPTM4B,MMRN1,DPYSL3,KIAAQ125组成的组。 CDK6,CPXM1,SOCS2,SMIM24,EMP1,NGFRAP1,CD34,AKR1C3,GPR56; 和(b)比较测试样品中至少3种基因的表达与来自一组患者对照样品的至少3种基因的参考表达水平; 其中使用测试样品中至少3种基因的表达和参考表达水平的差异或相似性来预测或分类具有AML的受试者成为低风险组或高风险组以生存更差。 p >
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公开(公告)号:EP3411517A1
公开(公告)日:2018-12-12
申请号:EP17746659.6
申请日:2017-02-06
Applicant: University Health Network
Inventor: WANG, Jean , DICK, John , NG, Stanley , MINDEN, Mark , MITCHELL, Amanda , CHEN, Weihsu, Claire , ZANDSTRA, Peter , KENNEDY, James
CPC classification number: G01N33/57426 , C12Q1/6883 , C12Q2600/106 , C12Q2600/118 , C12Q2600/158 , C40B40/06 , C40B40/08 , G01N2800/52 , G06F19/10 , G06F19/20
Abstract: There is described herein a method of prognosing or classifying a subject with acute myeloid leukemia (AML) comprising: (a) determining the expression level of at least 3 genes in a test sample from the subject selected from the group consisting of DNMT3B, ZBTB46, NYNRIN, ARHGAP22, LAPTM4B, MMRN1, DPYSL3, KIAAQ125. CDK6, CPXM1, SOCS2, SMIM24, EMP1, NGFRAP1, CD34, AKR1C3, GPR56; and (b) comparing expression of the at least 3 genes in the test sample with reference expression levels of the at least 3 genes from control samples from a cohort of patients; wherein a difference or similarity in the expression of the at least 3 genes in the test sample and the reference expression levels is used to prognose or classify the subject with AML into a low risk group or a high risk group for worse survival.
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