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人肝癌细胞中异常的半胱天冬酶激活的脱氧核糖核酸酶(CAD)转录本。

Aberrant caspase-activated DNase (CAD) transcripts in human hepatoma cells.

作者信息

Hsieh S Y, Liaw S F, Lee S N, Hsieh P S, Lin K H, Chu C M, Liaw Y F

机构信息

Liver Research Unit, Chang Gung Memorial Hospital, Taipei, Taiwan.

出版信息

Br J Cancer. 2003 Jan 27;88(2):210-6. doi: 10.1038/sj.bjc.6600695.

Abstract

The gene of caspase-activated DNase (CAD), the key enzyme for nucleosome cleavage during apoptosis, is mapped at chromosome 1p36, a region usually associated with hemizygous deletions in human cancers, particularly in hepatoma (HCC). It is tempting to speculate that CAD plays a tumour-suppressive role in hepatocarcinogenesis. To address this, we examined the CAD transcripts in six human HCC cell lines, one liver tissue from a non-HCC subject, and peripheral blood leukocytes (PBL) from three healthy individuals. Alternatively spliced CAD transcripts with fusion of exon 1 to exon 7 were isolated in most of the examined samples including HCC cells and normal controls. However, relatively abundant alternatively spliced CAD transcripts with fusion of exon 2 to exon 6 or 7, in which the corresponding domain directing CAD interaction with ICAD was preserved, were found only in poorly differentiated Mahlavu and SK-Hep1 cells. Interestingly, an abnormal CAD transcript with its exon 3 replaced by a truncated transposable Alu repeat was isolated in Hep3B cells, indicative of the implication of an Alu-mediated genomic mutation. Moreover, mis-sense mutations in the CAD genes were identified in all six HCC cell lines. Upon UV-induced apoptosis, DNA fragmentation efficiency was found to be intact, partially reduced and remarkably reduced in Huh7 and J328, Hep3B and HepG2, and Mahlavu cells, respectively. That mutations and aberrantly spliced transcripts for the CAD gene are frequently present in human HCC cells, especially in poorly differentiated HCC cells, suggests a significant role of CAD in human hepatocarcinogenesis.

摘要

半胱天冬酶激活的脱氧核糖核酸酶(CAD)基因是细胞凋亡过程中核小体裂解的关键酶,定位于1p36染色体区域,该区域通常与人类癌症尤其是肝癌(HCC)中的半合子缺失相关。因此很容易推测CAD在肝癌发生过程中发挥肿瘤抑制作用。为了验证这一点,我们检测了6种人类肝癌细胞系、1份非肝癌患者的肝组织以及3名健康个体外周血白细胞(PBL)中的CAD转录本。在包括肝癌细胞和正常对照在内的大多数检测样本中均分离出了外显子1与外显子7融合的可变剪接CAD转录本。然而,仅在低分化的Mahlavu和SK - Hep1细胞中发现了相对丰富的外显子2与外显子6或7融合的可变剪接CAD转录本,其中指导CAD与ICAD相互作用的相应结构域得以保留。有趣的是,在Hep3B细胞中分离出了一种异常的CAD转录本,其外显子3被截短的转座Alu重复序列取代,这表明存在Alu介导的基因组突变。此外,在所有6种肝癌细胞系中均鉴定出了CAD基因的错义突变。紫外线诱导细胞凋亡后,发现Huh7和J328、Hep3B和HepG2以及Mahlavu细胞中的DNA片段化效率分别保持完整、部分降低和显著降低。CAD基因的突变和异常剪接转录本在人类肝癌细胞中频繁出现,尤其是在低分化肝癌细胞中,这表明CAD在人类肝癌发生过程中具有重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b9a/2377037/a7be185f3de9/88-6600695f1.jpg

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