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乳腺癌耐药蛋白(BCRP)基因表达与儿童急性髓系白血病缓解诱导治疗反应不佳相关。

BCRP gene expression is associated with a poor response to remission induction therapy in childhood acute myeloid leukemia.

作者信息

Steinbach D, Sell W, Voigt A, Hermann J, Zintl F, Sauerbrey A

机构信息

University Children's Hospital, Jena, Germany.

出版信息

Leukemia. 2002 Aug;16(8):1443-7. doi: 10.1038/sj.leu.2402541.

Abstract

Breast cancer resistance protein (BCRP), also known as mitoxantrone resistance protein (MRX) or placenta ABC protein (ABC-P), is the second member of the ABCG subfamily of ABC transport proteins (gene symbol ABCG2). Transfection and enforced expression of BCRP in drug-sensitive cells confers resistance to mitoxantrone, doxorubicin, daunorubicin and topotecan. In this study the expression of BCRP gene was measured using TaqMan real-time PCR in 59 children with newly diagnosed AML. Nine patients were also analyzed in relapse. The median of BCRP gene expression was more than 10 times higher in patients who did not achieve remission after the first phase of chemotherapy (n = 24) as compared to patients who did achieve remission at this stage (n = 21; P = 0.012). In first relapse the expression of the BCRP gene was higher than at diagnosis (P = 0.038). Although high levels of BCRP gene expression were more frequent in subtypes of AML with a favorable prognosis, we found that within both risk groups (high and low risk), patients who expressed high levels of BCRP had a worse prognosis (P = 0.023). Our results strongly suggest that the expression of the BCRP gene reduces the response to chemotherapy in AML and that BCRP expression is higher at the time of relapse.

摘要

乳腺癌耐药蛋白(BCRP),也被称为米托蒽醌耐药蛋白(MRX)或胎盘ABC蛋白(ABC-P),是ABC转运蛋白ABCG亚家族的第二个成员(基因符号ABCG2)。在药物敏感细胞中转染并强制表达BCRP可赋予对米托蒽醌、阿霉素、柔红霉素和拓扑替康的耐药性。在本研究中,使用TaqMan实时PCR检测了59例新诊断急性髓系白血病(AML)患儿的BCRP基因表达。9例复发患者也进行了分析。与在化疗第一阶段达到缓解的患者(n = 21;P = 0.012)相比,在化疗第一阶段未达到缓解的患者(n = 24)中,BCRP基因表达中位数高出10倍以上。在首次复发时,BCRP基因表达高于诊断时(P = 0.038)。尽管BCRP基因高表达在预后良好的AML亚型中更常见,但我们发现在两个风险组(高风险和低风险)中,BCRP高表达的患者预后更差(P = 0.023)。我们的结果强烈表明,BCRP基因表达降低了AML对化疗的反应,且在复发时BCRP表达更高。

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