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促進上皮細胞間質轉型(EMT)、幹性及轉移的旁斑成分1(PSPC1)作為抗癌標的
专利权人:
ACADEMIA SINICA
发明人:
JOU, YUH-SHAN,周玉山,LANG, YAW-DONG,蓝耀东,藍耀東,YEH, HSI-WEN,叶希文,葉希文
申请号:
TW108104949
公开号:
TW201945020A
申请日:
2019.02.14
申请国别(地区):
TW
年份:
2019
代理人:
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.本發明揭示一種經分離之核酸,其編碼轉移的旁斑成分1(PSPC1)的C端片段。PSPC1的C端片段包含一大於10個但不超過131個胺基酸殘基的延伸,其中其C端胺基酸等同於PSPCl序列SEQ ID NO: 3的C端,且呈現對抗腫瘤細胞之生物活性。腫瘤細胞結合於PSPC1或蛋白質酪胺酸激酶6(PTK6)、或兩者。抗腫瘤活性係至少一選自於由:(a)抑制腫瘤細胞生長;(b)抑制腫瘤細胞進程;(c)抑制腫瘤細胞轉移;(d)減少PSPC1表達;以及(e)減少細胞質中致癌性PTK6的表達所組成群組。本發明亦揭示一種包含PSPC1之C端片段序列的胜肽。本發明亦揭示用於預測癌症病患之腫瘤進展、轉移、及預後的試劑套組及方法。
来源网站:
中国工程科技知识中心
来源网址:
http://www.ckcest.cn/home/
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