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前列腺癌中的多基因融合转录本和染色体重排。

Poly-gene fusion transcripts and chromothripsis in prostate cancer.

机构信息

Vancouver Prostate Centre and Department of Urologic Sciences, University of British Columbia, Vancouver, BC, Canada.

出版信息

Genes Chromosomes Cancer. 2012 Dec;51(12):1144-53. doi: 10.1002/gcc.21999. Epub 2012 Aug 25.

Abstract

Complex genome rearrangements are frequently observed in cancer but their impact on tumor molecular biology is largely unknown. Recent studies have identified a new phenomenon involving the simultaneous generation of tens to hundreds of genomic rearrangements, called chromothripsis. To understand the molecular consequences of these events, we sequenced the genomes and transcriptomes of two prostate tumors exhibiting evidence of chromothripsis. We identified several complex fusion transcripts, each containing sequence from three different genes, originating from different parts of the genome. One such poly-gene fusion transcript appeared to be expressed from a chain of small genomic fragments. Furthermore, we detected poly-gene fusion transcripts in the prostate cancer cell line LNCaP, suggesting they may represent a common phenomenon. Finally in one tumor with chromothripsis, we identified multiple mutations in the p53 signaling pathway, expanding on recent work associating aberrant DNA damage response mechanisms with chromothripsis. Overall, our data show that chromothripsis can manifest as massively rearranged transcriptomes. The implication that multigenic changes can give rise to poly-gene fusion transcripts is potentially of great significance to cancer genetics.

摘要

复杂的基因组重排经常在癌症中观察到,但它们对肿瘤分子生物学的影响在很大程度上是未知的。最近的研究发现了一种新的现象,涉及同时产生数十到数百个基因组重排,称为染色体重排。为了了解这些事件的分子后果,我们对两个表现出染色体重排证据的前列腺肿瘤进行了基因组和转录组测序。我们鉴定了几种复杂的融合转录本,每个转录本都包含来自基因组不同部分的三个不同基因的序列。这样的多基因融合转录本似乎是从一连串小的基因组片段表达而来的。此外,我们在前列腺癌细胞系 LNCaP 中检测到多基因融合转录本,表明它们可能代表一种常见现象。最后,在一个有染色体重排的肿瘤中,我们鉴定出 p53 信号通路中的多个突变,这扩展了最近将异常的 DNA 损伤反应机制与染色体重排联系起来的研究。总的来说,我们的数据表明染色体重排可以表现为大规模重排的转录组。多基因变化可能导致多基因融合转录本的出现,这对癌症遗传学具有潜在的重要意义。

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