Long noncoding RNA and mRNA profiling in cetuximab-resistant colorectal cancer cells by RNA sequencing analysis

被引:30
作者
Jing, Changwen [1 ,2 ,3 ]
Ma, Rong [1 ,2 ,3 ]
Cao, Haixia [1 ,2 ,3 ]
Wang, Zhuo [1 ,2 ,3 ]
Liu, Siwen [1 ,2 ,3 ]
Chen, Dan [1 ,2 ,3 ]
Wu, Yang [1 ,2 ,3 ]
Zhang, Junying [1 ,2 ,3 ]
Wu, Jianzhong [1 ,2 ,3 ]
机构
[1] Nanjing Med Univ, Jiangsu Canc Hosp, Clin Canc Res Ctr, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Jiangsu Inst Canc Res, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Med Univ, Affiliated Canc Hosp, Nanjing, Jiangsu, Peoples R China
关键词
cetuximab; colorectal cancer; lncRNA; mRNA; RNA-Seq; PROGNOSIS; THERAPY;
D O I
10.1002/cam4.2004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To gain an insight into the molecular mechanisms of cetuximab resistance in colorectal cancer, we generated a cetuximab-resistant cell line (H508/ CR) and performed RNA sequencing to identify the differential expression patterns of noncoding RNAs ( ncRNAs) and mRNAs between cetuximab-sensitive and resistant cells. A total of 278 ncRNA transcripts and 1,059 mRNA transcripts were dysregulated in the cetuximab- resistant cells. The expression levels of nine selected long noncoding RNAs ( lncRNAs) were validated using quantitative real-time PCR. Functional analysis revealed that several groups of lncRNAs might be involved in pathways associated with cetuximab resistance. Increased glucose consumption and lactate secretion in cetuximab-resistant cells suggested that glucose metabolism might be involved in cetuximab resistance. In addition, lncRNA LINC00973 was upregulated in the H508/ CR cell line and cells transfected with a LINC00973 short interfering RNA exhibited reduced cell viability, increased apoptosis, and decreased glucose consumption and lactate secretion. Our results provide essential data regarding differentially expressed lncRNAs and mRNAs in cetuximab-resistant cells, which may provide new potential candidates for cetuximab therapy.
引用
收藏
页码:1641 / 1651
页数:11
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