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Aberrant Methylation of LINE-1 Transposable Elements: A Search for Cancer Biomarkers

机译:DINE-1转置元素的异常甲基化:寻找癌症生物标志物

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摘要

Cancer remains one of the main causes of human mortality despite significant progress in its diagnostics and therapy achieved in the past decade. Massive hypomethylation of retrotransposons, in particular LINE-1, is considered a hallmark of most malignant transformations as it results in the reactivation of retroelements and subsequent genomic instability. Accumulating data on LINE-1 aberrant methylation in different tumor types indicates its significant role in cancer initiation and progression. However, direct evidence that LINE-1 activation can be used as a cancer biomarker is still limited. The objective of this review was to critically evaluate the published results regarding the diagnostic/prognostic potential of the LINE-1 methylation status in cancer. Our analysis indicates that LINE-1 hypomethylation is a promising candidate biomarker of cancer development, which, however, needs validation in both clinical and laboratory studies to confirm its applicability to different cancer types and/or stages. As LINE-1 is present in multiple cell-free copies in blood, it has advantages over single-copy genes regarding perspectives of using its methylation status as an epigenetic cancer biomarker for cell-free DNA liquid biopsy.
机译:癌症仍然是人类死亡率的主要原因之一,尽管在过去十年的诊断和治疗方面取得了显着进展。重复转换的大规模低甲基化,特别是线-1,被认为是最恶性转化的标志,因为它导致逆压力的再激活和随后的基因组不稳定性。在不同肿瘤类型中累积关于线 - 1异常甲基化的数据表明其在癌症起始和进展中的重要作用。然而,直接证据可以用作癌症生物标志物的直接证据仍然有限。本综述的目的是重新评估关于癌症中甲基化状态的诊断/预后潜力的公布结果。我们的分析表明,Line-1低甲基化是癌症发育的有希望的候选生物标志物,然而,在临床和实验室研究中需要验证,以证实其对不同癌症类型和/或阶段的适用性。由于线-1存在于血液中的多个无细胞拷贝中,它具有关于使用其甲基化状态作为外观遗传癌生物标志物的单拷贝基因的单拷贝基因的优势,用于无细胞DNA液体活组织检查。

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