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慢性粒细胞白血病中与长慢性期相关的bcr和c-abl分子异常。

Molecular abnormalities of bcr and c-abl in chronic myelogenous leukemia associated with a long chronic phase.

作者信息

Dreazen O, Berman M, Gale R P

机构信息

Department of Medicine, UCLA School of Medicine 90024.

出版信息

Blood. 1988 Mar;71(3):797-9.

PMID:2449925
Abstract

Median duration of the chronic phase of chronic myelogenous leukemia (CML) is 3 years; less than 20% of patients have a chronic phase greater than 7 years. It is unknown whether the length of chronic phase is stochastic or is predetermined for each patient. Since molecular abnormalities of bcr and c-abl occur in CML, we sought to determine whether there were differences in bcr and c-abl translocation or transcription in individuals with long v short chronic phase. These studies were performed in six patients with CML in whom chronic phase was 7+ to 26 years and 20 patients in whom chronic phase was less than 7 years. All patients had translocation of c-abl to within bcr. The distribution of breakpoints in bcr were similar in both groups. Transcription of the chimeric bcr/c-abl mRNA was comparable. These data suggest that changes in bcr or c-abl alone do not determine the duration of chronic phase in CML; other factors are likely involved.

摘要

慢性粒细胞白血病(CML)慢性期的中位持续时间为3年;不到20%的患者慢性期超过7年。慢性期的长度是随机的还是每个患者预先确定的尚不清楚。由于CML中存在bcr和c-abl的分子异常,我们试图确定慢性期长与短的个体在bcr和c-abl易位或转录方面是否存在差异。这些研究在6例慢性期为7年以上至26年的CML患者和20例慢性期小于7年的患者中进行。所有患者均有c-abl易位至bcr内。两组bcr中断点的分布相似。嵌合bcr/c-abl mRNA的转录相当。这些数据表明,仅bcr或c-abl的变化并不能决定CML慢性期的持续时间;可能涉及其他因素。

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