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公开(公告)号:US09889180B2
公开(公告)日:2018-02-13
申请号:US14443602
申请日:2013-11-19
Applicant: Agency for Science, Technology and Research
Inventor: Qiang Yu , Zhen Ning Wee
IPC: A61K31/713 , A61K31/706 , A61K31/437 , A61K38/21 , G01N33/574 , C07K16/40 , C07K14/57 , C12Q1/68 , C12N15/113
CPC classification number: A61K38/217 , A61K31/437 , A61K31/706 , A61K31/713 , C07K16/40 , C07K2317/76 , C12N15/1137 , C12N2310/14 , C12Q1/6886 , C12Y201/01043 , G01N33/57492 , G01N33/57496 , G01N2800/52 , A61K2300/00
Abstract: The present invention relates to a pharmaceutical composition comprising a histone-lysine N-methyltransferase EZH2 (enhancer of zeste homolog 2) inhibitor and an enhancer of interferon-gamma receptor activity. The invention also relates to method of treating a patient having cancer, comprising administration of the pharmaceutical composition.
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公开(公告)号:US20180311264A1
公开(公告)日:2018-11-01
申请号:US15770437
申请日:2016-10-24
Applicant: Agency for Science,Technology and Research
Inventor: Qiang Yu , Zhen Ning Wee
IPC: A61K31/704 , A61P35/00 , C12Q1/6886
CPC classification number: A61K31/704 , C12Q1/6886 , C12Q2600/106 , C12Q2600/118 , C12Q2600/158 , G01N33/57415 , G01N2333/5412 , G01N2333/5421 , G01N2800/52
Abstract: The present invention relates to the treatment of breast cancer, more particularly triple negative breast cancer (TNBC), with the use of an inhibitor of Interleukin 1 Receptor Associated Kinase 1 (IRAK1) such as ginsenosides. It also relates to a method for aiding in categorising or determining prognosis in a breast cancer patient or in selecting a therapeutic strategy comprising assessing the level of IRAK1 nucleic acid, protein or activity in a sample and, in some aspects, further assessing the paclitaxel resistance status of the patient and if the patient is resistant to paclitaxel therapy, treating the patient with an inhibitor of IRAK1 activity. In addition, a screening method for identifying a compound useful for treating breast cancer comprises determining the effect of a test compound on IRAK1 nucleic acid, protein or activity level and selecting a compound that reduces said level.
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公开(公告)号:US20140335106A1
公开(公告)日:2014-11-13
申请号:US14348365
申请日:2012-09-28
Applicant: Agency for Science, Technology and Research
Inventor: Qiang Yu , Shuet Theng Lee
IPC: C12N15/113 , A61K45/06 , A61K31/517 , C12Q1/68 , A61K31/519 , A61K31/47 , A61K31/4709 , A61K31/7088 , A61K31/5377
CPC classification number: C12N15/1135 , A61K31/47 , A61K31/4709 , A61K31/517 , A61K31/519 , A61K31/5377 , A61K31/7088 , A61K31/713 , A61K45/06 , C12N15/113 , C12N2310/14 , C12N2320/31 , C12Q1/6881 , C12Q2600/106 , A61K2300/00
Abstract: A method of treating cancer by inhibiting expression of ubiquitin associated and SH3 domain containing B (UBASH3B) gene or by inhibiting the activity of UBASH3B protein or a functional variant thereof.
Abstract translation: 通过抑制泛素相关和含有B(UBASH3B)基因的SH3结构域的表达或通过抑制UBASH3B蛋白或其功能变体的活性来治疗癌症的方法。
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公开(公告)号:US10881677B2
公开(公告)日:2021-01-05
申请号:US15770437
申请日:2016-10-24
Applicant: Agency for Science, Technology and Research
Inventor: Qiang Yu , Zhen Ning Wee
IPC: A61K31/704 , C12Q1/6886 , A61P35/00 , G01N33/574
Abstract: The present invention relates to the treatment of breast cancer, more particularly triple negative breast cancer (TNBC), with the use of an inhibitor of Interleukin 1 Receptor Associated Kinase 1 (IRAK1) such as ginsenosides. It also relates to a method for aiding in categorising or determining prognosis in a breast cancer patient or in selecting a therapeutic strategy comprising assessing the level of IRAK1 nucleic acid, protein or activity in a sample and, in some aspects, further assessing the paclitaxel resistance status of the patient and if the patient is resistant to paclitaxel therapy, treating the patient with an inhibitor of IRAK1 activity. In addition, a screening method for identifying a compound useful for treating breast cancer comprises determining the effect of a test compound on IRAK1 nucleic acid, protein or activity level and selecting a compound that reduces said level.
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5.
公开(公告)号:US09334500B2
公开(公告)日:2016-05-10
申请号:US14348365
申请日:2012-09-28
Applicant: Agency for Science, Technology and Research
Inventor: Qiang Yu , Shuet Theng Lee
IPC: C12N15/11 , C12N15/113 , A61K31/517 , A61K31/713 , A61K45/06 , A61K31/47 , A61K31/4709 , A61K31/5377 , A61K31/519 , A61K31/7088 , C12Q1/68
CPC classification number: C12N15/1135 , A61K31/47 , A61K31/4709 , A61K31/517 , A61K31/519 , A61K31/5377 , A61K31/7088 , A61K31/713 , A61K45/06 , C12N15/113 , C12N2310/14 , C12N2320/31 , C12Q1/6881 , C12Q2600/106 , A61K2300/00
Abstract: A method of treating cancer by inhibiting expression of ubiquitin associated and SH3 domain containing B (UBASH3B) gene or by inhibiting the activity of UBASH3B protein or a functional variant thereof.
Abstract translation: 通过抑制泛素相关和含有B(UBASH3B)基因的SH3结构域的表达或通过抑制UBASH3B蛋白或其功能变体的活性来治疗癌症的方法。
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公开(公告)号:US20150258175A1
公开(公告)日:2015-09-17
申请号:US14443602
申请日:2013-11-19
Applicant: Agency for Science, Technology and Research
Inventor: Qiang Yu , Zhen Ning Wee
IPC: A61K38/21 , C12N15/113 , C12Q1/68 , G01N33/574 , A61K31/437 , C07K16/40
CPC classification number: A61K38/217 , A61K31/437 , A61K31/706 , A61K31/713 , C07K16/40 , C07K2317/76 , C12N15/1137 , C12N2310/14 , C12Q1/6886 , C12Y201/01043 , G01N33/57492 , G01N33/57496 , G01N2800/52 , A61K2300/00
Abstract: The present invention relates to a pharmaceutical composition comprising a histone-lysine N-methyltransferase EZH2 (enhancer of zeste homolog 2) inhibitor and an enhancer of interferon-gamma receptor activity. The invention also relates to method of treating a patient having cancer, comprising administration of the pharmaceutical composition.
Abstract translation: 本发明涉及包含组蛋白赖氨酸N-甲基转移酶EZH2(泽斯特同系物2的增强子)抑制剂和干扰素-γ受体活性增强剂的药物组合物。 本发明还涉及治疗患有癌症的患者的方法,包括给药该药物组合物。
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公开(公告)号:US11680298B2
公开(公告)日:2023-06-20
申请号:US16331072
申请日:2017-09-07
Inventor: Qiang Yu , Jian Yuan Goh , Min Feng , Ern Yu Tan
IPC: C12Q1/68 , C12Q1/6886 , A61K31/519
CPC classification number: C12Q1/6886 , A61K31/519 , C12Q2600/112 , C12Q2600/156
Abstract: There is provided a method of identifying risk of cancer in a human subject, the method comprising: determining in a biological sample of the subject, whether a copy number amplification of at least one continuous genomic region specific to human chromosome 1q21 is present, wherein the presence of a copy number amplification of the region specific to human chromosome 1q21 represents an elevated risk of cancer in the subject and the at least one continuous genomic region is selected from the group consisting of: a human TUFT 1 gene or a gene from the human S100 family. It is also provided a method of treating cancer in a subject determined to have a copy number amplification of a region specific to human chromosome 1q21, the method comprising administering a therapeutic agent capable of suppressing IRAK1, IRAK4 or a S100 family member, such as Pacritinib. There are also provided a method of treating cancer, related polynucleotides, kits, therapeutic agents and use of the therapeutic agents.
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