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结直肠癌转移的全基因组DNA甲基化图谱

Landscape of Genome-Wide DNA Methylation of Colorectal Cancer Metastasis.

作者信息

Ili Carmen, Buchegger Kurt, Demond Hannah, Castillo-Fernandez Juan, Kelsey Gavin, Zanella Louise, Abanto Michel, Riquelme Ismael, López Jaime, Viscarra Tamara, García Patricia, Bellolio Enrique, Saavedra David, Brebi Priscilla

机构信息

Laboratory of Integrative Biology (LIBi), Centro de Excelencia en Medicina Traslacional (CEMT), Scientific and Technological Bioresource Nucleus (BIOREN), Universidad de La Frontera, Temuco 4810296, Chile.

Departamento Ciencias Básicas, Facultad de Medicina, Universidad de La Frontera, Temuco 4811230, Chile.

出版信息

Cancers (Basel). 2020 Sep 22;12(9):2710. doi: 10.3390/cancers12092710.

Abstract

Colorectal cancer is a heterogeneous disease caused by both genetic and epigenetics factors. Analysing DNA methylation changes occurring during colorectal cancer progression and metastasis formation is crucial for the identification of novel epigenetic markers of patient prognosis. Genome-wide methylation sequencing of paired samples of colon (normal adjacent, primary tumour and lymph node metastasis) showed global hypomethylation and CpG island (CGI) hypermethylation of primary tumours compared to normal. In metastasis we observed high global and non-CGI regions methylation, but lower CGI methylation, compared to primary tumours. Gene ontology analysis showed shared biological processes between hypermethylated CGIs in metastasis and primary tumours. After complementary analysis with The Cancer Genome Atlas (TCGA) cohort, , , , and genes were found associated with poor survival. We mapped the methylation landscape of colon normal tissues, primary tumours and lymph node metastasis, being capable of identified methylation changes throughout the genome. Furthermore, we found five genes with potential for methylation biomarkers of poor prognosis in colorectal cancer patients.

摘要

结直肠癌是一种由遗传和表观遗传因素共同引起的异质性疾病。分析结直肠癌进展和转移形成过程中发生的DNA甲基化变化对于识别患者预后的新型表观遗传标志物至关重要。对结肠配对样本(正常相邻组织、原发性肿瘤和淋巴结转移灶)进行全基因组甲基化测序显示,与正常组织相比,原发性肿瘤呈现整体低甲基化和CpG岛(CGI)高甲基化。在转移灶中,与原发性肿瘤相比,我们观察到整体和非CGI区域的甲基化程度较高,但CGI甲基化程度较低。基因本体分析显示转移灶和原发性肿瘤中高甲基化CGI之间存在共同的生物学过程。在与癌症基因组图谱(TCGA)队列进行补充分析后,发现 、 、 、 和 基因与不良生存相关。我们绘制了结肠正常组织、原发性肿瘤和淋巴结转移灶的甲基化图谱,能够识别全基因组的甲基化变化。此外,我们发现了五个有潜力作为结直肠癌患者预后不良甲基化生物标志物的基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0450/7564781/05d31788a206/cancers-12-02710-g001.jpg

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