发明名称 Prostate cancer-specific alterations in ERG gene expression and detection and treatment methods based on those alterations
摘要 Alterations in ERG gene expression can be observed in patients with prostate cancer. Specific ERG isoforms are associated with, or involved in, prostate cancer. Compositions comprising these isoforms provide therapeutic benefit and can be used in methods of detecting, diagnosing, prognosing, and treating prostate cancer. These compositions provide biomarkers for detecting the expression of combinations of the PSA/KLK3, PMEPA1, NKX3.1, ODC1, AMD1, and ERG genes.
申请公布号 US9206481(B2) 申请公布日期 2015.12.08
申请号 US200812081101 申请日期 2008.04.10
申请人 The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc. 发明人 Srivastava Shiv;Dobi Albert;Sreenath Taduru;Petrovics Gyorgy;Sun Chen
分类号 C12Q1/68 主分类号 C12Q1/68
代理机构 MH2 Technology Law Group, LLP 代理人 MH2 Technology Law Group, LLP
主权项 1. A method of detecting the expression of Ets Related Gene 8 (ERG8) mRNA in a biological sample comprising nucleic acid sample isolated from human prostate epithelial cells, the method comprising: (a) combining the nucleic acid sample isolated from human prostate epithelial cells with at least a first and a second oligonucleotide primer under hybridizing conditions, wherein the first and the second oligonucleotide primers amplify a target sequence comprising a 3′ non-coding region within nucleotides 1311 to 2441 of SEQ ID NO: 30, and wherein the entire nucleotide sequence of at least one of the first or the second oligonucleotide primers hybridizes to a region within said nucleotides 1311 to 2441 of SEQ ID NO:30 or a nucleic acid strand complementary to said region; (b) amplifying a plurality of amplification products when said nucleotides 1311 to 2441 of SEQ ID NO:30 are present in the nucleic acid sample by adding at least one polymerase activity to the biological sample containing the first and second oligonucleotide primers, wherein the amplification products comprises the region within nucleotides 1311 to 2441 of SEQ ID NO: 30 to which the entire nucleotide sequence of at least one of the first or the second oligonucleotide primers hybridizes; (c) immobilizing the plurality of amplification products; (d) combining an oligonucleotide probe with the immobilized plurality of amplification products to thereby permit the probe to hybridize to at least one immobilized amplification product; (e) detecting whether a signal results from hybridization between the oligonucleotide probe and at least one amplification product, and (f) detecting expression of ERG8 mRNA in the biological sample if the signal is detected in step (e).
地址 Bethesda MD US