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癌症中染色体易位断裂点区域的潜在 G-四链体形成可能解释了它们的脆弱性。

Potential G-quadruplex formation at breakpoint regions of chromosomal translocations in cancer may explain their fragility.

机构信息

Department of Biochemistry, Indian Institute of Science, Bangalore-560 012, India.

出版信息

Genomics. 2012 Aug;100(2):72-80. doi: 10.1016/j.ygeno.2012.05.008. Epub 2012 May 30.

Abstract

Genetic alterations like point mutations, insertions, deletions, inversions and translocations are frequently found in cancers. Chromosomal translocations are one of the most common genomic aberrations associated with nearly all types of cancers especially leukemia and lymphoma. Recent studies have shown the role of non-B DNA structures in generation of translocations. In the present study, using various bioinformatic tools, we show the propensity of formation of different types of altered DNA structures near translocation breakpoint regions. In particular, we find close association between occurrence of G-quadruplex forming motifs and fragile regions in almost 70% of genes involved in rearrangements in lymphoid cancers. However, such an analysis did not provide any evidence for the occurrence of G-quadruplexes at the close vicinity of translocation breakpoint regions in nonlymphoid cancers. Overall, this study will help in the identification of novel non-B DNA targets that may be responsible for generation of chromosomal translocations in cancer.

摘要

基因突变,如点突变、插入、缺失、倒位和易位,在癌症中经常被发现。染色体易位是与几乎所有类型的癌症(尤其是白血病和淋巴瘤)相关的最常见的基因组异常之一。最近的研究表明,非 B-DNA 结构在易位的产生中起作用。在本研究中,我们使用各种生物信息学工具,显示了在易位断点区域附近形成不同类型改变的 DNA 结构的倾向。特别是,我们发现,在涉及淋巴癌重排的基因中,约 70%的基因中存在 G-四链体形成基序和脆弱区域之间存在密切关联。然而,这种分析并没有为非淋巴癌中易位断点区域附近发生 G-四链体提供任何证据。总的来说,这项研究将有助于确定可能导致癌症中染色体易位产生的新型非 B-DNA 靶标。

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