Suppr超能文献

[维甲酸与急性早幼粒细胞白血病]

[Retinoids and acute promyelocytic leukemia].

作者信息

Hashimoto Y, Shudo K

机构信息

Institute of Applied Microbiology, University of Tokyo.

出版信息

Gan To Kagaku Ryoho. 1991 Oct;18(13):2203-9.

PMID:1656889
Abstract

Retinoic acid and its analogs, retinoids, have been shown to be useful in the treatment of several types of tumors. Retinoids elicit their biological activities by binding to their specific nuclear receptors, denoted as RAR-alpha, beta and gamma. RAR's have been established to be retinoid-dependent transcription factors which belong to the steroid/thyroid nuclear receptor superfamily. Recently, retinoic acid has been reported to be extremely effective in the treatment of acute promyelocytic leukemia (APL) giving more than 70% complete remission efficiency. APL has been characterized by the specific chromosomal translocation, t(15;17). Analysis of the t(15;17) breaking point revealed that (i) either RAR-alpha on chromosome 17 or the gene named myl on chromosome 15 is abnormal in APL cells, and (ii) the abnormal fused protein myl/RAR-alpha is expressed, which is suspected to cause the APL. Thus, RAR-alpha gene may be now regarded as one of tumor suppressor genes.

摘要

维甲酸及其类似物类视黄醇已被证明可用于治疗多种类型的肿瘤。类视黄醇通过与它们特定的核受体(称为RAR-α、β和γ)结合来发挥其生物活性。RAR已被确定为依赖视黄酸的转录因子,属于类固醇/甲状腺核受体超家族。最近,据报道维甲酸在治疗急性早幼粒细胞白血病(APL)方面极其有效,完全缓解率超过70%。APL的特征是特定的染色体易位t(15;17)。对t(15;17)断裂点的分析表明:(i)在APL细胞中,17号染色体上的RAR-α或15号染色体上名为myl的基因是异常的;(ii)异常的融合蛋白myl/RAR-α被表达,怀疑它会导致APL。因此,RAR-α基因现在可能被视为肿瘤抑制基因之一。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验