聚合酶链反应在血液学恶性肿瘤中检测活化癌基因的应用。

F Ishikawa, Y Kobayashi
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引用次数: 0

摘要

应用聚合酶链反应(PCR)检测血液学恶性肿瘤和白血病前期癌基因激活的结构变化。采用寡核苷酸差异杂交联用PCR检测N-ras癌基因点突变。17例AML患者中有5例显示有N-ras基因突变。这些突变可作为残留恶性细胞诊断的遗传标记。采用cDNA合成和PCR技术对CML的费城染色体进行了检测。PCR是一种高度通用和敏感的方法,在临床诊断中具有不可估量的价值。
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Application of polymerase chain reaction to detect activated oncogenes in hematological malignancies.

Polymerase chain reaction (PCR) was applied to detect the structural change accompanying the activation of oncogenes in hematological malignancies and preleukemic states. Point mutation of N-ras oncogene was examined by oligonucleotide differential hybridization coupled with PCR. Five out of 17 AML patients were shown to have mutated N-ras gene. These mutations could be used as a genetic marker to diagnose the residual malignant cells. Philadelphia chromosome in CML was examined by cDNA synthesis and PCR with successful results. PCR was shown to be a highly versatile and sensitive method which would be invaluable in clinical diagnosis.

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The hematopoietic system [Application of nucleolar organizer region staining technique to air-dried blood smears]. [Biochemical and molecular biological studies on beta-glucuronidase in myelogenous leukemic cells]. [Production and secretion of BSF2/IL6 in a case of hairy cell leukemia with polyclonal hypergammaglobulinemia]. [Long-term cultures of marrow cells from the patients with aplastic anemia].
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