Novel Role of Base Excision Repair and Mismatch Repair in Cisplatin Sensitivity
Novel Role of Base Excision Repair and Mismatch Repair in Cisplatin Sensitivity
批准号:
8436233
负责人:
Steve M Patrick
金额:
$15.72万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-03-15 至 2014-01-31
关键词:
AddressAffectAftercareAntineoplastic AgentsApoptosisBase Excision RepairsBindingBiochemicalBiological AssayCell Cycle ArrestCell LineCellsCisplatinClinicClinicalComplementCytosineDNADNA AdductsDNA DamageDNA Interstrand Cross-Link RepairDNA RepairDNA Repair PathwayDNA StructureDNA biosynthesisDataDeaminationDependenceDevelopmentDisease remissionDrug TargetingDrug resistanceEffectivenessEnzymesGenetic TranscriptionGoalsHead and Neck CancerHead and neck structureHealthHumanIn VitroKnockout MiceLeadLyaseMalignant NeoplasmsMalignant neoplasm of lungMediatingMismatch RepairMitomycinsModelingMonitorMutationNatureNucleotide Excision RepairNull LymphocytesOvarianPathway interactionsPharmaceutical PreparationsPhenotypePlatinumPlayProcessProtein BindingProteinsResistanceRoleSiteStructureTechniquesTestingTreatment ProtocolsUracilWorkadductbasecancer cellcancer recurrencecancer therapycrosslinkcytotoxiccytotoxicitydesigninhibitor/antagonistkillingsmethoxyaminemutantneoplastic cellnoveloxaliplatinprotein complexrepairedresistance mechanismsynthetic constructtransplatinuracil-DNA glycosylase
中文摘要
说明(申请人提供):顺铂是应用最广泛的化疗药物之一。它主要用于治疗睾丸癌、卵巢癌、头颈部癌和肺癌。顺铂的细胞毒性作用归因于DNA加合物阻断了参与DNA复制和DNA转录的酶。这些加合物导致细胞周期停滞,最终导致细胞凋亡。然而,在癌症治疗和缓解后,往往会出现复发和对顺铂耐药的情况。肿瘤细胞中这种耐药的一个主要机制是增强DNA修复。这项建议侧重于在顺铂疗效中发挥作用的途径。我们假设碱基切除修复(BER)和错配修复(MMR)在维持顺铂敏感性方面发挥重要作用,这是通过依赖于链间交联链(ICL)的独特机制实现的。这一机制是通过ICL的特殊结构处理和与ICL受损DNA的“实际”修复竞争来实现的。为了解决我们的假设,我们将进行以下具体目标:1)阐明BER蛋白在顺铂敏感性和ICL修复中的作用;2)确定MMR蛋白在顺铂敏感性、ICL修复和突变避免中的作用;3)使用体外技术和纯化的蛋白质来进一步评估BER和MMR蛋白在顺铂ICL加工过程中的生化机制。了解参与顺铂疗效的途径和癌细胞克服药物的机制是至关重要的。这对于设计更好的治疗方案以及开发新的抗癌药物是当务之急。如果没有这种认识,新的癌症治疗方法的发展是有限的。
英文摘要
DESCRIPTION (provided by applicant): Cisplatin is one of the most widely used chemotherapeutic drugs. It is primarily used in the treatment of testicular, ovarian, head and neck and lung cancers. The cytotoxic effects of cisplatin have been attributed to DNA adducts which block the enzymes involved in DNA replication and DNA transcription. These adducts cause cell cycle arrest which eventually leads to apoptosis. Frequently, however, after treatment and remission of the cancer, recurrence and resistance to cisplatin occurs. A major mechanism of this resistance in tumor cells is enhanced DNA repair. This proposal focuses on the pathways that play a role in cisplatin effectiveness. We hypothesize that base excision repair (BER) and mismatch repair (MMR) play vital roles in maintaining cisplatin sensitivity through a unique mechanism that is dependent on interstrand cross-links (ICLs). This mechanism is mediated through specific structural processing of the ICLs and competition with 'actual' repair of the ICL damaged DNA. To address our hypothesis, we will conduct the following specific aims 1) elucidate the role of BER proteins in cisplatin sensitivity and ICL repair; 2) determine the role of MMR proteins in cisplatin sensitivity, ICL repair and mutation avoidance; and 3) use in vitro techniques and purified proteins to further assess the biochemical mechanisms of BER and MMR proteins in cisplatin ICL processing. It is critical to understand the pathways involved in cisplatin efficacy and mechanisms that cancer cells develop to overcome the drug. This is imperative for the design of better treatment protocols as well as in the development of new anticancer agents. Without this understanding, the development of new cancer treatment is limited.
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