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ARYL HYDROCARBON RECEPTOR (AHR) ACTIVATOR COMPOUNDS AS CANCER THERAPEUTICS

机译:芳基烃受体(AHR)活化剂化合物作为癌症治疗剂

摘要

The present disclosure relates to compositions and methods for the diagnosis and treatment or prevention of cancers, particularly cancers that exhibit elevated expression of FOXA1 and/or FOXA1 gene targets, such as certain breast, liver and/or prostate cancers, including luminal and/or ER-positive forms of breast cancer. Three previously identified adenosine receptor antagonists, CGS-15943, MRS-1220 and SCH-58261, as well as furan ring moiety-possessing derivatives of CGS-15943 are specifically provided for killing cancer cells in a manner that appears to involve activation of the aryl hydrocarbon receptor (AHR) by such compounds. The instant disclosure therefore provides for selecting and/or administering CGS-15943, MRS-1220, SCH-58261 and/or a furan-possessing derivative of CGS-15943, MRS-1220 and/or SCH-58261 as a therapeutic agent to target a cancer cell and/or subject having or at risk of developing a cancer. Methods and compositions for therapies that include such compounds are also provided
机译:本公开涉及用于诊断和治疗或预防癌症的组合物和方法,特别是表现出富氧化率升高的癌症的癌症,例如某些乳腺癌,肝脏和/或前列腺癌,包括腔和/或ER-正面形式的乳腺癌。三个以前鉴定的腺苷受体拮抗剂,CGS-15943,MRS-1220和SCH-58261以及CGS-15943的具有呋喃环部分的衍生物,以以似乎涉及激活芳基的方式杀死癌细胞通过这些化合物(AHR)的烃受体(AHR)。因此,本发明提供了用于选择和/或施用CGS-15943,MRS-1220,SCH-58261和/或具有CGS-15943,MRS-1220和/或SCH-58261的呋喃 - 具有衍生物作为靶标的治疗剂具有或有患癌症的癌细胞和/或受试者。还提供了包括这些化合物的疗法的方法和组合物

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