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Enhancer of cell predation for use in sensitizing tumors to radiation therapy

机译:细胞捕食增强剂,用于使肿瘤对放射治疗敏感

摘要

The present invention relates to the use of the compounds shown in Tables 1 and 2 and analogs thereof for promoting IR media cell phagocytosis in cancer cells. The compounds are referred to herein as "promoters of IR media cell phagocytosis." The compounds can be used to enhance tumor immunogenicity and / or induce a significant protective anti-cancer immune response in a subject that will or will receive radiation therapy. In other words, the compounds can be used to enhance radiation therapy in a subject in need thereof. The compound is preferably mebuhiroline 1,5-naphthalenedisulfonic acid salt, flurbiprofen, minaprine dihydrochloride, myricetin, digoxin, digitoxin, lanatoside, LOPA87, VP331, RN-1-026, SG6163F, VP450 and VP43. Selected from the group consisting of:
机译:本发明涉及表1和2中所示的化合物及其类似物在促进癌细胞中IR培养基细胞吞噬作用中的用途。该化合物在本文中被称为“ IR培养基细胞吞噬作用的促进剂”。所述化合物可用于增强将要或将要接受放射治疗的受试者的肿瘤免疫原性和/或诱导显着的保护性抗癌免疫应答。换句话说,所述化合物可用于在需要其的受试者中增强放射疗法。所述化合物优选为甲布洛林1,5-萘二磺酸盐,氟比洛芬,米那林二盐酸盐,杨梅素,地高辛,洋地黄毒苷,镧系元素,LOPA87,VP331,RN-1-026,SG6163F,VP450和VP43。从以下组成的组中选择:

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