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Ph阳性慢性髓性白血病祖细胞对bcr-abl转录的研究。

Investigation of bcr-abl transcription by Ph-positive chronic myeloid leukemia progenitors.

作者信息

Keating A

机构信息

Toronto Hospital, Ontario, Canada.

出版信息

Stem Cells. 1993 Oct;11 Suppl 3:31-3. doi: 10.1002/stem.5530110910.

Abstract

It is now feasible to investigate bcr-abl transcription by the progeny of Ph-positive (Ph+) early and committed hemopoietic progenitor cells from patients with chronic myeloid leukemia (CML). Cells from individual colonies can be bisected and each half analyzed by cytogenetics or the reverse transcriptase-polymerase chain reaction (RT-PCR) method to detect the bcr-abl transcript using internal nested oligonucleotide primers that flank the chimeric gene junction. We previously showed that some Ph+ colonies have undetectable PCR products for bcr-abl. When colonies are generated in the presence of alpha interferon (IFN-alpha) bcr-abl transcripts are undetectable in the majority of Ph+ colonies. These data suggest a potential mechanism for the action of IFN-alpha in Ph+ CML and indicate the need for a combined approach with cytogenetics and RT-PCR in analyzing the bcr-abl gene.

摘要

现在,通过慢性粒细胞白血病(CML)患者的Ph阳性(Ph+)早期和定向造血祖细胞的后代来研究bcr-abl转录是可行的。来自单个集落的细胞可以一分为二,每一半通过细胞遗传学或逆转录聚合酶链反应(RT-PCR)方法进行分析,使用位于嵌合基因连接处两侧的内部巢式寡核苷酸引物来检测bcr-abl转录本。我们之前表明,一些Ph+集落无法检测到bcr-abl的PCR产物。当在α干扰素(IFN-α)存在的情况下产生集落时,大多数Ph+集落中无法检测到bcr-abl转录本。这些数据提示了IFN-α在Ph+ CML中发挥作用的潜在机制,并表明在分析bcr-abl基因时需要将细胞遗传学和RT-PCR结合起来。

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