Kotliar N, Koziner B
Unidad de Investigaciones Oncohematológicas-ONCOLAB, Buenos Aires, Argentina.
Medicina (B Aires). 1995;55(2):159-66.
The early detection of clonogenic cells able to survive cytotoxic therapy and to initiate a neoplastic process, defined as Minimal Residual Disease (MRD), represents a major objective for the development of new and more sensitive diagnostic methods. The cloning of different chromosomal translocations along with the application of the Polymerase Chain Reaction (PCR) technique has allowed the characterization of various hematological disorders at the molecular level. This approach has led to the development of PCR based assays able to detect a minimum number of malignant cells with very high specificity. In the present paper we discuss the use of PCR and its value as a predictor for relapse in lymphomas, chronic myelogenous leukemia and acute promyelocytic leukemia, characterized by the t(14;18) t(9;22) and t(15;17) translocations, respectively.
能够在细胞毒性治疗后存活并引发肿瘤过程的克隆源性细胞的早期检测,即微小残留病(MRD),是开发更新、更敏感诊断方法的主要目标。不同染色体易位的克隆以及聚合酶链反应(PCR)技术的应用,使得在分子水平上对各种血液系统疾病进行特征描述成为可能。这种方法促成了基于PCR的检测方法的发展,该方法能够以非常高的特异性检测到最少数量的恶性细胞。在本文中,我们讨论了PCR的应用及其作为淋巴瘤、慢性粒细胞白血病和急性早幼粒细胞白血病复发预测指标的价值,这些疾病分别以t(14;18)、t(9;22)和t(15;17)易位为特征。