Comprehensive genome- and transcriptome-wide analyses of mutations associated with microsatellite instability in Korean gastric cancers

被引:50
作者
Yoon, Kwiyeom [1 ]
Lee, Sunghoon [2 ,3 ]
Han, Tae-Su [4 ]
Moon, So Yeon [1 ]
Yun, Sun Mi [1 ,5 ]
Kong, Seong-Ho [4 ,6 ]
Jho, Sungwoong [2 ]
Choe, Jinny [1 ]
Yu, Jieun [4 ]
Lee, Hyuk-Joon [4 ,6 ]
Park, Ji Hyun [1 ]
Kim, Hak-Min [2 ]
Lee, So Yeun [1 ]
Park, Jongsun [2 ]
Kim, Woo-Ho [4 ,7 ]
Bhak, Jong [2 ,3 ]
Yang, Han-Kwang [4 ,6 ]
Kim, Seong-Jin [1 ,5 ]
机构
[1] CHA Univ, CHA Canc Inst, Seoul 135081, South Korea
[2] Genome Res Fdn, Personal Genom Inst, Suwon 443270, South Korea
[3] TheragenEtex Bio Inst Inc, Suwon 443270, South Korea
[4] Seoul Natl Univ, Canc Res Inst, Seoul 110799, South Korea
[5] CHA Univ, Coll Life Sci, Dept Biomed Sci, Seoul 135081, South Korea
[6] Seoul Natl Univ, Coll Med, Dept Surg, Seoul 110799, South Korea
[7] Seoul Natl Univ, Coll Med, Dept Pathol, Seoul 110799, South Korea
基金
新加坡国家研究基金会;
关键词
MESSENGER-RNA DECAY; SOMATIC MUTATIONS; MONONUCLEOTIDE REPEATS; 3'-UNTRANSLATED REGION; BETA RECEPTOR; COLON; GENES; EXPRESSION; IDENTIFICATION; SEQUENCES;
D O I
10.1101/gr.145706.112
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Microsatellite instability (MSI) is a critical mechanism that drives genetic aberrations in cancer. To identify the entire MS mutation, we performed the first comprehensive genome- and transcriptome-wide analyses of mutations associated with MSI in Korean gastric cancer cell lines and primary tissues. We identified 18,377 MS mutations of five or more repeat nucleotides in coding sequences and untranslated regions of genes, and discovered 139 individual genes whose expression was down-regulated in association with UTR MS mutation. In addition, we found that 90.5% of MS mutations with deletions in gene regions occurred in UTRs. This analysis emphasizes the genetic diversity of MSI-H gastric tumors and provides clues to the mechanistic basis of instability in microsatellite unstable gastric cancers.
引用
收藏
页码:1109 / 1117
页数:9
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