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胸苷酸合成酶药物遗传学

Thymidylate synthase pharmacogenetics.

作者信息

Marsh Sharon

机构信息

Division of Molecular Oncology, Washington University School of Medicine in St. Louis, 660, South Euclid Avenue, Campus Box 8069, St. Louis, MO 63110, USA.

出版信息

Invest New Drugs. 2005 Dec;23(6):533-7. doi: 10.1007/s10637-005-4021-7.

Abstract

Thymidylate synthase (TYMS) is an important target for chemotherapy drugs, such as 5-fluorouracil (5FU) and methotrexate. Over-expression of TYMS is linked to resistance to TYMS-targeted chemotherapy drugs. Currently there is no protocol for selecting cancer patients at risk for drug resistance prior to chemotherapy treatment. Three polymorphisms in the 5' and 3' untranslated regions (5'UTR and 3'UTR) of the thymidylate synthase gene have been shown to influence TYMS expression. Preliminary data has suggested a poorer response rate to 5FU or methotrexate is seen in patients with 3 copies of a 28 bp tandem repeat in the 5'UTR enhancer region (TSER polymorphism) and this relationship may be further clarified by the presence of a single nucleotide polymorphism (SNP) with the second repeat of the 3 repeat (TSER(*)3) allele. A 6 bp deletion in the 3'UTR of the TYMS gene has also been shown to affect TYMS RNA expression and has a significant association with poor outcome in 5FU treated patients. Evidence linking all 3 TYMS polymorphisms with TYMS expression and patient response to TYMS-targeted chemotherapy treatment will be highlighted.

摘要

胸苷酸合成酶(TYMS)是化疗药物(如5-氟尿嘧啶(5FU)和甲氨蝶呤)的重要靶点。TYMS的过表达与对靶向TYMS的化疗药物的耐药性有关。目前,在化疗治疗前,尚无针对有耐药风险的癌症患者进行选择的方案。胸苷酸合成酶基因5'和3'非翻译区(5'UTR和3'UTR)中的三种多态性已被证明会影响TYMS的表达。初步数据表明,5'UTR增强子区域存在28 bp串联重复序列的3个拷贝(TSER多态性)的患者对5FU或甲氨蝶呤的反应率较低,并且这种关系可能会因3个重复序列(TSER(*)3)等位基因的第二个重复序列存在单核苷酸多态性(SNP)而进一步得到阐明。TYMS基因3'UTR中的一个6 bp缺失也已被证明会影响TYMS RNA的表达,并且与5FU治疗患者的不良预后有显著关联。将重点介绍将所有3种TYMS多态性与TYMS表达以及患者对靶向TYMS的化疗治疗反应联系起来的证据。

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