Stirewalt Derek L, Meshinchi Soheil, Kussick Steven J, Sheets Kayla M, Pogosova-Agadjanyan Era, Willman Cheryl L, Radich Jerald P
Clinical Research Division, Fred Hutchinson Cancer Research Center, and Division of Oncology, University of Washington, Seattle, WA 98109, USA.
Br J Haematol. 2004 Feb;124(4):481-4. doi: 10.1111/j.1365-2141.2004.04808.x.
Internal tandem duplications in FLT3 are the most common mutation in acute myeloid leukaemia (AML), with agarose gel electrophoresis of polymerase chain reaction products (PCR/agarose) being the screening method of choice for these mutations. As PCR/agarose screening does not detect small mutations, single-stranded conformational polymorphism analyses (PCR/SSCP) were used in an attempt to identify previously unrecognized point mutations in FLT3 exons 14 and 15 of 140 AML patients, using newly designed primers that anneal within intron sequences. Novel missense point mutations were found in exon 14, suggesting additional investigations should be performed in AML and other haematopoietic malignancies, using this sensitive technique.
FLT3内部串联重复是急性髓系白血病(AML)中最常见的突变,聚合酶链反应产物的琼脂糖凝胶电泳(PCR/琼脂糖)是检测这些突变的首选筛查方法。由于PCR/琼脂糖筛查无法检测到小的突变,因此使用单链构象多态性分析(PCR/SSCP),通过新设计的在内含子序列内退火的引物,试图鉴定140例AML患者FLT3外显子14和15中先前未识别的点突变。在外显子14中发现了新的错义点突变,这表明应使用这种敏感技术,对AML和其他血液系统恶性肿瘤进行进一步研究。