Goh Hyun-Gyung, Hwang Ji-Yeon, Kim Soo-Hyun, Lee Young-Hoon, Kim Yoo-Li, Kim Dong-Wook
Division of Hematology, St. Mary's Hospital, The Catholic University of Korea, Youngdeungpo-gu, Seoul, Korea.
Transl Res. 2006 Nov;148(5):249-56. doi: 10.1016/j.trsl.2006.07.002.
Diagnosis of chronic myeloid leukemia (CML) is based on the detection of BCR-ABL gene or Philadelphia chromosome (Ph chromosome), and fusion proteins with different sizes are encoded depending on the breakpoint in the BCR gene. In general, 3 breakpoint cluster regions in the BCR gene have been described: major (M-bcr), minor (m-bcr), and micro (mu-bcr). This study was designed to determine the frequency of BCR-ABL transcripts using one-step multiplex reverse transcription polymerase chain reaction (RT-PCR). Bone marrow (BM) or peripheral blood (PB) samples at diagnosis from 548 patients were obtained with a referring diagnosis of Ph-positive (Ph+) CML, and multistep RT-PCR and newly developed one-step multiplex RT-PCR were applied on each sample. Compared with the previous multistep RT-PCR, one-step multiplex RT-PCR with the primers is the more rapid and accurate method to identify the BCR-ABL breakpoints. Most patients (538/548, 98.18%) were found to have b3a2 or b2a2, and total frequency of occurrence of c3a2, e1a2, b2a3, b1a1, and e1a3 or coexpression of b2a2 and b3a2 was less than 2.00%. No differences were observed between women and men. As the multiplex RT-PCR technique distinguishes BCR-ABL transcripts in all samples with high sensitivity and specificity, it easily could be applied at early stages of diagnosis. The incidence of one or the other rearrangement in CML patients varies in different reported series, and the frequency in each type of BCR-ABL transcript in Korean CML patients seems to be different from those of Western countries.
慢性髓性白血病(CML)的诊断基于BCR-ABL基因或费城染色体(Ph染色体)的检测,根据BCR基因中的断点可编码不同大小的融合蛋白。一般来说,已描述了BCR基因中的3个断点簇区域:主要(M-bcr)、次要(m-bcr)和微小(μ-bcr)。本研究旨在使用一步多重逆转录聚合酶链反应(RT-PCR)确定BCR-ABL转录本的频率。从548例诊断为Ph阳性(Ph+)CML的患者中获取诊断时的骨髓(BM)或外周血(PB)样本,并对每个样本应用多步RT-PCR和新开发的一步多重RT-PCR。与之前的多步RT-PCR相比,使用引物的一步多重RT-PCR是鉴定BCR-ABL断点更快速、准确的方法。大多数患者(538/548,98.18%)被发现有b3a2或b2a2,c3a2、e1a2、b2a3、b1a1和e1a3的总发生率或b2a2和b3a2的共表达低于2.00%。未观察到男女之间的差异。由于多重RT-PCR技术能以高灵敏度和特异性区分所有样本中的BCR-ABL转录本,因此很容易应用于诊断早期。CML患者中一种或另一种重排的发生率在不同报道系列中有所不同,韩国CML患者中每种类型BCR-ABL转录本的频率似乎与西方国家不同。