Methods for detecting predisposition to cancer at the MTS gene
    1.
    发明授权
    Methods for detecting predisposition to cancer at the MTS gene 失效
    检测MTS基因癌症易感性的方法

    公开(公告)号:US5989815A

    公开(公告)日:1999-11-23

    申请号:US848251

    申请日:1997-04-29

    IPC分类号: A01N61/00 C07H21/02 C12Q1/68

    CPC分类号: A01N61/00 C07H21/02 C12Q1/68

    摘要: The present invention relates to somatic mutations in the Multiple Tumor Suppressor (MTS) gene in human cancers and their use in the diagnosis and prognosis of human cancer. The invention further relates to germ line mutations in the MTS gene and their use in the diagnosis of predisposition to melanoma, leukemia, astrocytoma, glioblastoma, lymphoma, glioma, Hodgkin's lymphoma, CLL, and cancers of the pancreas, breast, thyroid, ovary, uterus, testis, kidney, stomach and rectum. The invention also relates to the therapy of human cancers which have a mutation in the MTS gene, including gene therapy, protein replacement therapy and protein mimetics. Finally, the invention relates to the screening of drugs for cancer therapy.

    摘要翻译: 本发明涉及人类癌症中多重肿瘤抑制因子(MTS)基因的体细胞突变及其在人类癌症诊断和预后中的应用。 本发明还涉及MTS基因中的种系突变及其在诊断黑素瘤,白血病,星形细胞瘤,成胶质细胞瘤,淋巴瘤,胶质瘤,霍奇金淋巴瘤,CLL和胰腺,乳腺,甲状腺,卵巢癌, 子宫,睾丸,肾,胃和直肠。 本发明还涉及在MTS基因中具有突变的人类癌症的治疗,包括基因治疗,蛋白质替代疗法和蛋白质模拟物。 最后,本发明涉及用于癌症治疗的药物的筛选。