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环境介导的耐药性:多发性骨髓瘤治疗的靶点。

Environmental-mediated drug resistance: a target for multiple myeloma therapy.

机构信息

Departments of Experimental Therapeutics and Oncologic Sciences, H. Lee Moffitt Cancer Center and Research Institute, University of South Florida, 12902 Magnolia Drive, Tampa, FL 33612, USA.

出版信息

Expert Rev Hematol. 2009 Dec;2(6):649-62. doi: 10.1586/ehm.09.55.

Abstract

Multiple myeloma is an incurable malignancy of mature clonal B cells. The refractory nature of this disease has long been attributed to the acquisition of drug resistance. Traditionally, mechanisms of drug resistance have been defined by genetic, acquired changes in the expression or function of specific genes products. However, over the past 10 years a large body of evidence has emerged demonstrating that in addition to mechanisms of drug resistance intrinsic to the cancer cell, there exist dynamic, de novo mechanisms coordinated by the tumor microenvironment resulting in a environmental-mediated drug resistance (EM-DR). Within this review we will provide an overview of some of these mechanisms of drug resistance and how they contribute to minimal residual disease and subsequent treatment failure. By understanding mechanisms of EM-DR, therapeutic targets can be identified and interventions designed to reduce minimal residual disease and improve clinical outcomes.

摘要

多发性骨髓瘤是一种不可治愈的成熟克隆 B 细胞恶性肿瘤。这种疾病的难治性长期以来归因于获得性耐药。传统上,耐药机制是通过特定基因产物的表达或功能的遗传获得性改变来定义的。然而,在过去的 10 年中,大量证据表明,除了癌细胞固有的耐药机制外,还存在由肿瘤微环境协调的动态、新出现的机制,导致环境介导的耐药性(EM-DR)。在这篇综述中,我们将概述一些耐药机制以及它们如何导致微小残留病和随后的治疗失败。通过了解 EM-DR 的机制,可以确定治疗靶点,并设计干预措施来减少微小残留病并改善临床结果。

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