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Analysis of the Thymidylate Synthase Gene Structure in Colorectal Cancer Patients and Its Possible Relation with the 5-Fluorouracil Drug Response

机译:结直肠癌患者胸苷酸合酶基因结构分析及其与5-氟尿嘧啶药物反应的可能关系

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摘要

Thymidylate synthase (TS) catalyzes methylation of dUMP to dTMP and it is the target for the 5-Fluorouracil (5-FU) activity. Barbour et al. showed that variant structural forms of TS in tumour cell lines confer resistance to fluoropyrimidines. We planned to perform the whole TS gene structure by means of sequencing techniques in human colorectal cancer (CRC) samples to try to identify the presence of any possible TS variant form that could be responsible of fluoropyrimidines drug resistance and of the worse prognosis. We performed the TS-DNA gene sequence in 68 CRC from patients of A, B, and C Dukes' stages and different histological grade, but we did not find any mutation in the TS-DNA structure. In the future we intend to widen the TS structure analysis to the metastatic CRCs, because due to their higher genomic instability, they could present a TS variant form responsible of the fluoropyrimidines drug resistance and the worse prognosis.
机译:胸苷酸合酶(TS)催化dUMP甲基化为dTMP,它是5-氟尿嘧啶(5-FU)活性的目标。巴伯等。结果表明,肿瘤细胞系中TS的变异结构形式赋予了对氟嘧啶的抗性。我们计划通过人类大肠癌(CRC)样品中的测序技术来执行整个TS基因结构,以尝试鉴定可能导致氟嘧啶耐药性和预后不良的任何TS变异形式。我们在68位来自A,B和C杜克氏癌分期和不同组织学级别的患者的CRC中进行了TS-DNA基因序列的分析,但我们未发现TS-DNA结构中的任何突变。将来,我们打算将TS结构分析扩展到转移性CRC,因为它们的基因组更高 不稳定,他们可能会提供TS变体形式 负责氟嘧啶的耐药性 和预后更差。

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