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韩国患者结直肠癌靶向测序的突变特征分析

Mutational Characterization of Colorectal Cancer from Korean Patients with Targeted Sequencing.

作者信息

Lee Jongmin, Choi Sangtae, Jung Donghae, Jung YunJae, Kim Jung Ho, Jung Sungwon, Lee Won-Suk

机构信息

Gachon Institute of Genome Medicine and Science, Gachon University Gil Medical Center, Incheon, Republic of Korea.

Gachon Advanced Institute for Health Science and Technology, Gachon University, Incheon, Republic of Korea.

出版信息

J Cancer. 2021 Oct 28;12(24):7300-7310. doi: 10.7150/jca.61324. eCollection 2021.

Abstract

Effective treatment of colorectal cancer could benefit from understanding molecular characteristics including mutation profiles of important genes. This study aimed to explore the molecular characteristics of colorectal cancer based on next generation sequencing. The mutational characteristics by targeted next generation sequencing in 172 colorectal tumor samples from Korean patients were evaluated to explore their associations with clinical features. Targeted sequencing of 375 genes was performed with an average target-depth of 800X. TP53 and APC showed higher mutation frequencies from the left-sided tumors, while CTNNB1 were more frequent from the right-sided tumors. The tumor suppressor NOTCH1 and the DNA strand break repair gene PALB2 were more frequently mutated in early onset tumors. KRAS and PTEN mutations were more frequent from patients with advanced cancers by cancer antigen markers. TP53 and BRAF mutations were more frequent from patients of T3 and T4 stages, where their variant allele fractions were generally higher in T4 tumors, implying that advanced tumors have higher fraction of cancer cells with TP53 and BRAF mutations. Mutational profiles of these patients were also assessed with other clinical features. Comparison of mutational characteristics with the Caucasian subjects from independent data showed that the identified mutational characteristics are largely Korean-specific except for a few key colorectal cancer genes. Next generation sequencing-based targeted sequencing can provide valuable information on molecular characterization of colorectal cancer patients, and its clinically relevant information can provide benefits to better understand colorectal cancer.

摘要

了解包括重要基因的突变谱在内的分子特征,可能有助于结直肠癌的有效治疗。本研究旨在基于二代测序探索结直肠癌的分子特征。对172例韩国患者的结直肠肿瘤样本进行靶向二代测序,评估其突变特征,以探索它们与临床特征的关联。对375个基因进行靶向测序,平均靶向深度为800倍。TP53和APC在左侧肿瘤中显示出较高的突变频率,而CTNNB1在右侧肿瘤中更常见。肿瘤抑制因子NOTCH1和DNA链断裂修复基因PALB2在早发性肿瘤中更频繁地发生突变。根据癌症抗原标志物,KRAS和PTEN突变在晚期癌症患者中更常见。TP53和BRAF突变在T3和T4期患者中更频繁,其中T4肿瘤中它们的变异等位基因分数通常更高,这意味着晚期肿瘤中具有TP53和BRAF突变的癌细胞比例更高。还根据其他临床特征评估了这些患者的突变谱。将突变特征与来自独立数据的白种人受试者进行比较,结果显示,除了少数关键的结直肠癌基因外,所确定的突变特征在很大程度上是韩国人特有的。基于二代测序的靶向测序可为结直肠癌患者的分子特征提供有价值的信息,其临床相关信息有助于更好地了解结直肠癌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31a6/8734410/809cb777b2fc/jcav12p7300g001.jpg

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