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RAR-α基因重排作为急性早幼粒细胞白血病诊断和监测的遗传标志物。

RAR-alpha gene rearrangements as a genetic marker for diagnosis and monitoring in acute promyelocytic leukemia.

作者信息

Biondi A, Rambaldi A, Alcalay M, Pandolfi P P, Lo Coco F, Diverio D, Rossi V, Mencarelli A, Longo L, Zangrilli D

机构信息

Clinica Pediatrica Università di Milano, Ospedale S. Gerardo, Monza, Italy.

出版信息

Blood. 1991 Apr 1;77(7):1418-22.

PMID:1849030
Abstract

Acute promyelocytic leukemias (APLs) are characterized by a translocation that involves chromosomes 15 and 17. The translocation breakpoints have recently been identified and shown to involve the RAR-alpha gene on 17 and myl on 15. Here we report Southern blotting analysis of 26 APLs, including cases with normal karyotypes and atypical morphology, which showed RAR-alpha rearrangements in 92% cases, myl rearrangements in 73%, and either RAR-alpha or myl rearrangements in 100%. Despite a negative clinical and morphologic picture, DNA rearrangement analysis showed that neoplastic promyelocytes persisted in the bone marrow of two patients sampled after induction chemotherapy. Therefore, the RAR-alpha and myl rearrangements provide molecular markers for accurately diagnosing APLs and monitoring the course of the disease during and after chemotherapy.

摘要

急性早幼粒细胞白血病(APL)的特征是涉及15号和17号染色体的易位。最近已确定了易位断点,显示其涉及17号染色体上的RAR-α基因和15号染色体上的myl基因。在此,我们报告了对26例APL进行的Southern印迹分析,包括核型正常和形态不典型的病例,结果显示92%的病例有RAR-α重排,73%有myl重排,100%有RAR-α或myl重排。尽管临床和形态学表现为阴性,但DNA重排分析显示,两名诱导化疗后取样的患者骨髓中仍存在肿瘤性早幼粒细胞。因此,RAR-α和myl重排为准确诊断APL以及监测化疗期间和化疗后的疾病进程提供了分子标志物。

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