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FUSION GENES ASSOCIATED WITH PROGRESSIVE PROSTATE CANCER

机译:与前列腺癌相关的融合基因

摘要

The present invention relates to methods and compositions for determining whether a subject having prostate cancer is at greater risk of developing progressive disease, and methods of treating the subjects. It is based, at least in part, on the discovery that approximately 90% of men carrying at least one of the following fusion genes: TRMT11-GRIK2, SLC45A2-AMACR, MTOR-TP53BP1, LRRC59-FLJ60017, TMEM135-CCDC67 and CCNH-C5orf30 experienced prostate cancer recurrence, metastases and/or prostate cancer-specific death after radical prostatectomy (each examples of “progressive prostate cancer”), while these outcomes occurred in only 36% of men not carrying any of these fusion genes. It is also based, at least in part, on the discovery that no patient studied survived five years without recurrence if their primary prostate cancer contained a TRMT11-GRIK2 or MTOR-TP53BP1 fusion gene. It is also based, at least in part, on the discovery that the protein encoded by the MAN2A1-FER fusion gene exhibits kinase activity.
机译:本发明涉及用于确定患有前列腺癌的受试者是否处于进行性疾病的更大风险的方法和组合物,以及治疗该受试者的方法。该发现至少部分基于以下发现:大约90%的男性携带至少以下融合基因之一:TRMT11-GRIK2,SLC45A2-AMACR,MTOR-TP53BP1,LRRC59-FLJ60017,TMEM135-CCDC67和CCNH- C5orf30在根治性前列腺切除术后经历了前列腺癌的复发,转移和/或特定于前列腺癌的死亡(每个例子为“进行性前列腺癌”),而只有36%的男性未携带任何这些融合基因时发生了这些结果。这也至少部分基于以下发现:如果他们的原发性前列腺癌包含TRMT11-GRIK2或MTOR-TP53BP1融合基因,则没有研究的患者可以存活5年且无复发。它还至少部分基于以下发现:由MAN2A1-FER融合基因编码的蛋白质表现出激酶活性。

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