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依托泊苷对白血病细胞中两种半胱天冬酶-2 mRNA 亚型的差异影响。

Differential influence of etoposide on two caspase-2 mRNA isoforms in leukemic cells.

作者信息

Wotawa Anne, Solier Stéphanie, Logette Emmanuelle, Solary Eric, Corcos Laurent

机构信息

INSERM U517, IFR 100, Faculty of Medicine, 7 boulevard Jeanne d'Arc, 21000, Dijon, France.

出版信息

Cancer Lett. 2002 Nov 28;185(2):181-9. doi: 10.1016/s0304-3835(02)00287-2.

Abstract

Etoposide (VP-16) is an anticancer agent that induces apoptosis in human leukemic cell lines such as U937 and HL60. We performed RNase protection assays, with two distinct cRNA panels covering most of caspase and BCL-2-related genes, using total RNA from cell lines exposed to various concentrations of the drug. Our results show that VP-16 down-regulates expression of most surveyed genes with the noticeable exception of casp-2S mRNA that is up regulated whereas casp-2L mRNA is decreased. Since these mRNAs are produced by the alternative splicing of exon 9, we devised a reverse transcriptase-polymerase chain reaction method using primers from exons 8 and 10 to demonstrate that VP-16 stimulates the production of exon 9-containing sequences, irrespective of active transcription. However, this effect is specific of the 3'-end of the CASP-2 gene since no difference in the relative amounts of the 5'-end of the mRNA species is detected. Nevertheless, the level of full-length casp-2L mRNA together with that of procaspase-2L protein, which is pro-apoptotic, are decreased under VP-16 treatment, suggesting that an early cell response to treatment by cytotoxic agents is to down-regulate expression of selected pro-apoptotic proteins.

摘要

依托泊苷(VP - 16)是一种抗癌药物,可诱导人白血病细胞系(如U937和HL60)发生凋亡。我们使用来自暴露于不同浓度该药物的细胞系的总RNA,进行了核糖核酸酶保护分析,使用了两个不同的覆盖大多数半胱天冬酶和BCL - 2相关基因的cRNA组。我们的结果表明,VP - 16下调了大多数检测基因的表达,但显著例外的是casp - 2S mRNA上调,而casp - 2L mRNA减少。由于这些mRNA是由外显子9的可变剪接产生的,我们设计了一种逆转录聚合酶链反应方法,使用来自外显子8和10的引物来证明VP - 16刺激含外显子9序列的产生,而与活性转录无关。然而,这种效应是CASP - 2基因3'端特有的,因为未检测到mRNA种类5'端相对量的差异。尽管如此,在VP - 16处理下,全长casp - 2L mRNA水平以及具有促凋亡作用的procaspase - 2L蛋白水平均降低,这表明细胞对细胞毒性药物处理的早期反应是下调选定促凋亡蛋白的表达。

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