Lin Ming-Tseh, Tseng Li-Hui, Beierl Katie, Harada Shuko, Hafez Michael J, Eshleman James R, Gocke Christopher D
Department of Pathology, Johns Hopkins University School of Medicine, Johns Hopkins Hospital, Baltimore, Maryland, USA.
Diagn Mol Pathol. 2011 Dec;20(4):194-202. doi: 10.1097/PDM.0b013e31821dac16.
Polymorphic short tandem repeat (STR), or microsatellite, loci have been widely used to analyze chimerism status after allogeneic hematopoietic stem cell transplantation. The presence of a patient's DNA, as identified by STR analysis, may indicate residual or recurrent malignant disease or may represent normal hematopoiesis of patient origin. The ratio of patient-derived to donor-derived alleles is used to calculate the relative amount of patient cells (both benign and malignant) to donor cells. STRs on chromosomes known to be gained or lost in a patient's tumor are generally ignored because it is difficult to perform meaningful calculations of mixed chimerism. However, in this study, we present evidence that STR loci on gained or lost chromosomes are useful in distinguishing the benign or malignant nature of chimeric DNA. In the peripheral blood or bone marrow of 4 hematopoietic stem cell transplantation patients with leukemia or lymphoma, we identified tumor DNA on the basis of STR loci showing copy number alteration. We propose that a targeted evaluation of STR loci showing altered copy number in posttransplant chimerism analysis can provide evidence of residual cancer cells.
多态性短串联重复序列(STR),即微卫星位点,已被广泛用于分析异基因造血干细胞移植后的嵌合状态。通过STR分析鉴定出的患者DNA的存在,可能表明残留或复发性恶性疾病,也可能代表患者来源的正常造血。患者来源与供体来源等位基因的比例用于计算患者细胞(包括良性和恶性)与供体细胞的相对数量。已知在患者肿瘤中获得或丢失的染色体上的STR通常被忽略,因为难以对混合嵌合体进行有意义的计算。然而,在本研究中,我们提供证据表明,获得或丢失染色体上的STR位点有助于区分嵌合DNA的良性或恶性性质。在4例患有白血病或淋巴瘤的造血干细胞移植患者的外周血或骨髓中,我们基于显示拷贝数改变的STR位点鉴定出肿瘤DNA。我们提出,在移植后嵌合分析中对显示拷贝数改变的STR位点进行靶向评估,可以提供残留癌细胞的证据。