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急性髓系白血病中ATP结合盒转运蛋白的表达:与体外细胞毒性及预后标志物的关联

ATP-binding casette transporter expression in acute myeloid leukemia: association with in vitro cytotoxicity and prognostic markers.

作者信息

Varatharajan Savitha, Abraham Ajay, Karathedath Sreeja, Ganesan Sukanya, Lakshmi Kavitha M, Arthur Nancy, Srivastava Vivi M, George Biju, Srivastava Alok, Mathews Vikram, Balasubramanian Poonkuzhali

机构信息

Department of Haematology, Christian Medical College, Vellore, India.

Cytogenetics Unit, Christian Medical College, Vellore, India.

出版信息

Pharmacogenomics. 2017 Feb;18(3):235-244. doi: 10.2217/pgs-2016-0150. Epub 2017 Jan 23.

Abstract

INTRODUCTION

Drug resistance and relapse are considered to be the major reasons for treatment failure in acute myeloid leukemia (AML). There is limited data on the role of ABC transporter expression on in vitro sensitivity to cytarabine (Ara-C) and daunorubicin (Dnr) in primary AML cells.

PATIENTS & METHODS: RNA expression levels of 12 ABC transporters were analyzed by real-time quantitative PCR in 233 de novo adult acute myeloid leukemia patients. Based on cytarabine or Dnr IC, the samples were categorized as sensitive, intermediate and resistant. Role of candidate ABC transporter RNA expression on in vitro cytotoxicity, treatment outcome post therapy as well as the influence of various prognostic markers on ABC transporter expression were analyzed.

RESULTS

Expression of ABCC3 and ABCB6 were significantly higher in Dnr-resistant samples when compared with Dnr-sensitive samples. Increased ABCC1 expression was associated with poor disease-free survival in this cohort of patients.

CONCLUSION

This comprehensive analysis suggests ABCC1, ABCC3, ABCB6 and ABCA5 as probable targets which can be modulated for improving chemotherapeutic responses.

摘要

引言

耐药性和复发被认为是急性髓系白血病(AML)治疗失败的主要原因。关于ABC转运蛋白表达对原发性AML细胞体外对阿糖胞苷(Ara-C)和柔红霉素(Dnr)敏感性的作用的数据有限。

患者与方法

通过实时定量PCR分析了233例初发成年急性髓系白血病患者中12种ABC转运蛋白的RNA表达水平。根据阿糖胞苷或柔红霉素的IC,将样本分为敏感、中度和耐药。分析了候选ABC转运蛋白RNA表达对体外细胞毒性、治疗后治疗结果的作用以及各种预后标志物对ABC转运蛋白表达的影响。

结果

与Dnr敏感样本相比,Dnr耐药样本中ABCC3和ABCB6的表达显著更高。在这组患者中,ABCC1表达增加与无病生存期差相关。

结论

这项综合分析表明ABCC1、ABCC3、ABCB6和ABCA5可能是可调节的靶点,以改善化疗反应。

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