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晚期乳腺癌中多药耐药基因1(MDR1)和胸苷酸合成酶(TS)基因表达:与药物暴露、p53突变及患者临床结局的关系

MDR1 and thymidylate synthase (TS) gene expressions in advanced breast cancer: relationships to drug exposure, p53 mutations, and clinical outcome of the patients.

作者信息

Lizard-Nacol S, Genne P, Coudert B, Riedinger J M, Arnal M, Sancy C, Brunet-Lecomte P, Fargeot P

机构信息

Centre Georges François Leclerc, Dijon, France.

出版信息

Anticancer Res. 1999 Jul-Aug;19(4C):3575-81.

Abstract

To characterize the biological features of advanced breast cancer associated with poor chemotherapy response and worse prognosis, sequential tumor samples obtained from 75 patients receiving primary chemotherapy were analysed for MDR1 and TS gene expression before and after treatment. MDR1 gene expression was also analysed in 36 sequential normal samples. The levels of MDR1 and TS genes expression were determined by reverse transcription-PCR method, and examined in relation to p53 gene status, and the clinical outcome of the patients. After treatment, MDR1 expression levels were significantly enhanced in tumor (p = 0.0033) and normal (p = 0.0098) samples, whereas a significant decrease in TS expression was observed (p = 0.0054). There was no significant correlation between MDR1 or TS expressions and the presence of p53 mutations (detected in 24% of the cases), chemoresponsiveness, or survival. Only p53 mutations were associated with reduced disease-free survival (p = 0.0473). These results demonstrate that MDR1 and TS gene expressions were affected by drug exposure, but not by p53 gene status. Furthermore, the increase of MDR1 gene expression in normal and tumor tissues is in favor of an induced MDR1 expression rather than of a selection of resistant tumoral clones, which can be responsible for the absence of relationship of MDR1 expression with clinical outcome of advanced breast cancer patients.

摘要

为了表征与化疗反应差和预后较差相关的晚期乳腺癌的生物学特征,对75例接受一线化疗的患者在治疗前后获取的系列肿瘤样本进行了多药耐药基因1(MDR1)和胸苷酸合成酶(TS)基因表达分析。还对36份系列正常样本进行了MDR1基因表达分析。采用逆转录-聚合酶链反应(RT-PCR)方法测定MDR1和TS基因的表达水平,并结合p53基因状态及患者的临床结局进行分析。治疗后,肿瘤样本(p = 0.0033)和正常样本(p = 0.0098)中的MDR1表达水平显著升高,而TS表达则显著下降(p = 0.0054)。MDR1或TS的表达与p53突变(24%的病例检测到)、化疗反应或生存率之间无显著相关性。仅p53突变与无病生存期缩短相关(p = 0.0473)。这些结果表明MDR1和TS基因表达受药物暴露影响,但不受p53基因状态影响。此外,正常组织和肿瘤组织中MDR1基因表达的增加支持诱导性MDR1表达,而非耐药肿瘤克隆的选择,这可能是MDR1表达与晚期乳腺癌患者临床结局缺乏相关性的原因。

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