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散发性中国结直肠癌的体细胞突变图谱。

The landscape of somatic mutation in sporadic Chinese colorectal cancer.

作者信息

Liu Zhe, Yang Chao, Li Xiangchun, Luo Wen, Roy Bhaskar, Xiong Teng, Zhang Xiuqing, Yang Huanming, Wang Jian, Ye Zhenhao, Chen Yang, Song Jinghe, Ma Shuai, Zhou Yong, Yang Min, Fang Xiaodong, Du Jie

机构信息

Beijing Anzhen Hospital, Capital Medical University, The Key Laboratory of Remodeling-Related Cardiovascular Diseases, Ministry of Education, Beijing Collaborative Innovation Center for Cardiovascular Disorders, Beijing Institute of Heart, Lung and Blood Vessel Disease, Beijing, China.

Beijing Advanced Innovation Center for Big Data and Brain Computing (BDBC), Beihang University, Beijing, China.

出版信息

Oncotarget. 2018 Jun 8;9(44):27412-27422. doi: 10.18632/oncotarget.25287.

Abstract

Colorectal cancer is the fifth prevalent cancer in China. Nevertheless, a large-scale characterization of Chinese colorectal cancer mutation spectrum has not been carried out. In this study, we have performed whole exome-sequencing analysis of 98 patients' tumor samples with matched pairs of normal colon tissues using Illumina and Complete Genomics high-throughput sequencing platforms. Canonical CRC somatic gene mutations with high prevalence (>10%) have been verified, including , , , , and . is identified as a novel frequently mutated gene (10.6%). APC and Wnt signaling exhibit significantly lower mutation frequencies than those in TCGA data. Analysis with clinical characteristics indicates that gene and Wnt signaling display lower mutation rate in lymph node positive cancer than negative ones, which are not observed in TCGA data. gene and Wnt signaling are considered as the key molecule and pathway for colorectal cancer initiation, and these findings greatly undermine their importance in tumor progression for Chinese patients. Taken together, the application of next-generation sequencing has led to the determination of novel somatic mutations and alternative disease mechanisms in colorectal cancer progression, which may be useful for understanding disease mechanism and personalizing treatment for Chinese patients.

摘要

结直肠癌是中国第五大常见癌症。然而,尚未对中国结直肠癌突变谱进行大规模表征。在本研究中,我们使用Illumina和Complete Genomics高通量测序平台,对98例患者的肿瘤样本及其配对的正常结肠组织进行了全外显子组测序分析。已验证了高患病率(>10%)的典型结直肠癌体细胞基因突变,包括 、 、 、 、 和 。 被鉴定为一个新的高频突变基因(10.6%)。APC和Wnt信号通路的突变频率显著低于TCGA数据中的频率。临床特征分析表明, 基因和Wnt信号通路在淋巴结阳性癌症中的突变率低于阴性癌症,这在TCGA数据中未观察到。 基因和Wnt信号通路被认为是结直肠癌起始的关键分子和途径,而这些发现极大地削弱了它们在中国患者肿瘤进展中的重要性。综上所述,下一代测序的应用已导致确定了结直肠癌进展中的新体细胞突变和替代疾病机制,这可能有助于理解疾病机制并为中国患者进行个性化治疗。

需注意,原文中部分基因名称未完整给出,翻译时用“ ”代替。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e561/6007951/1be730ba7843/oncotarget-09-27412-g001.jpg

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