首页> 外国专利> PARASPECKLE COMPONENT 1 (PSPC1) PROMOTING EPITHELIAL-MESENCHYMAL TRANSITION, STEMNESS AND METASTASIS AS AN ANTI-CANCER TARGET

PARASPECKLE COMPONENT 1 (PSPC1) PROMOTING EPITHELIAL-MESENCHYMAL TRANSITION, STEMNESS AND METASTASIS AS AN ANTI-CANCER TARGET

机译:花生四烯酸化合物1(PSPC1)促进上皮-间质转化,茎突和转移成为抗癌靶标

摘要

An isolated nucleic acid encoding a C-terminal fragment of paraspeckle component 1 (PSPC1) is disclosed. The C-terminal fragment of the PSPC1 comprises an extension of more than 10 but no greater than 131 amino acid residues with its C-terminal amino acid identical to the C-terminus of the PSPC1 sequence SEQ ID NO: 3 and exhibits a biological activity against tumor cells. The tumor cells are associated with either PSPC1 or protein tyrosine kinase 6 (PTK6), or both. The anti-tumor activity is at least one selected from the group consisting of: (a) suppressing tumor cell growth; (b) suppressing tumor cell progression; (c) suppressing tumor cell metastasis; (d) decreasing PSPC1 expression; and (e) decreasing oncogenic PTK6 expression in cytoplasm. Also disclosed is a peptide comprising a C-terminal fragment sequence of PSPC1. A reagent kit and method for predicting tumor progression, metastasis, and prognosis in a cancer patient are also disclosed.
机译:公开了分离的编码副斑点组分1(PSPC1)的C-末端片段的核酸。 PSPC1的C末端片段包含超过10个但不超过131个氨基酸残基的延伸,其C末端氨基酸与PSPC1序列SEQ ID NO:3的C末端相同,并表现出生物学活性。针对肿瘤细胞。肿瘤细胞与PSPC1或蛋白酪氨酸激酶6(PTK6)或两者相关。抗肿瘤活性是选自以下的至少一种:(a)抑制肿瘤细胞的生长; (b)抑制肿瘤细胞的进展; (c)抑制肿瘤细胞转移; (d)降低PSPC1表达; (e)降低细胞质中致癌PTK6的表达。还公开了包含PSPC1的C末端片段序列的肽。还公开了用于预测癌症患者中的肿瘤进展,转移和预后的试剂盒和方法。

著录项

  • 公开/公告号WO2019160840A1

    专利类型

  • 公开/公告日2019-08-22

    原文格式PDF

  • 申请/专利权人 ACADEMIA SINICA;SHIH MING-CHE;

    申请/专利号WO2019US17591

  • 发明设计人 JOU YUH-SHAN;LANG YAW-DONG;YEH HSI-WEN;

    申请日2019-02-12

  • 分类号A61K38/01;A61K38/17;C07K14/435;C07K14/47;

  • 国家 WO

  • 入库时间 2022-08-21 11:53:33

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