Kang Ho-Young, Hwang Ji-Yeon, Kim Su-Hyun, Goh Hyun-gyung, Kim Myungshin, Kim Dong-Wook
Division of Hematology, Uijeongbu St. Mary's Hospital, The Catholic University of Korea, 65-1 Kumoh-dong, Ujeongbu-si, Kyonggi-do, Korea.
Haematologica. 2006 May;91(5):659-62. Epub 2006 Apr 19.
To identify a fast and sensitive method for screening for mutations in patients with imatinib- resistant chronic myeloid leukemia (CML), we compared allele specific oligonucleotide- polymerase chain reaction (ASO-PCR) assay with conventional direct sequencing. Among the 68 imatinib resistant CML patients studied, 18 amino acid substitutions were detected in 44 patients by two assays. The sensitivity of ASO-PCR was superior to that of direct sequencing as it could detect one mutant allele in 100 approximately 100,000 wild type sequences. The fastness, simplicity, and sensitivity of ASO-PCR assays will be useful for routine monitoring of mutations, especially for frequently identified mutations.
为了确定一种快速且灵敏的方法来筛查伊马替尼耐药慢性髓性白血病(CML)患者的突变,我们将等位基因特异性寡核苷酸聚合酶链反应(ASO-PCR)检测与传统直接测序法进行了比较。在所研究的68例伊马替尼耐药CML患者中,两种检测方法在44例患者中检测到了18个氨基酸替代。ASO-PCR的灵敏度优于直接测序法,因为它能够在大约100,000个野生型序列中检测到1个突变等位基因。ASO-PCR检测的快速性、简便性和灵敏性将有助于对突变进行常规监测,尤其是对于经常鉴定出的突变。