RNA processing genes characterize RNA splicing and further stratify colorectal cancer

被引:3
|
作者
Lu, Xiaofan [1 ]
Zhou, Yujie [2 ]
Meng, Jialin [3 ,4 ,5 ]
Jiang, Liyun [1 ,6 ]
Gao, Jun [1 ]
Cheng, Yu [1 ]
Yan, Hangyu [1 ]
Wang, Yang [7 ]
Zhang, Bing [7 ]
Li, Xiaobo [2 ]
Yan, Fangrong [1 ]
机构
[1] China Pharmaceut Univ, Res Ctr Biostat & Computat Pharm, State Key Lab Nat Med, Nanjing, Peoples R China
[2] Shanghai Jiao Tong Univ, Key Lab Gastroenterol & Hepatol, Div Gastroenterol & Hepatol, Shanghai Inst Digest Dis,Minist Hlth,Renji Hosp,S, Shanghai, Peoples R China
[3] Anhui Med Univ, Inst Urol, Affiliated Hosp 1, Dept Urol, Hefei, Peoples R China
[4] Anhui Med Univ, Anhui Prov Key Lab Genitourinary Dis, Hefei, Peoples R China
[5] Univ Rochester, Med Ctr, Dept Pathol & Urol, Rochester, NY 14642 USA
[6] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[7] Nanjing Univ, Affiliated Nanjing Drum Tower Hosp, Med Sch, Dept Radiol, Nanjing, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
alternative splicing events; colorectal cancer; prognostic value; restricted mean survival; RNA processing genes; DNA-DAMAGE; GENOME STABILITY; R PACKAGE; SURVIVAL; EXPRESSION; SIGNATURE; METASTASIS; SRSF1; DYSREGULATION; ACTIVATION;
D O I
10.1111/cpr.12861
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Objectives Due to the limited evaluation of the prognostic value of RNA processing genes (RPGs), which are regulators of alternative splicing events (ASEs) that have been shown to be associated with tumour progression, this study sought to determine whether colorectal cancer (CRC) could be further stratified based on the expression pattern of RPGs. Materials and Methods The gene expression profiles of CRCs were collected from TCGA (training set) and three external validation cohorts, representing 1060 cases totally. Cox regression with least absolute shrinkage and selection operator (LASSO) penalty was used to develop an RNA processing gene index (RPGI) risk score. Kaplan-Meier curves, multivariate Cox regression and restricted mean survival (RMS) analyses were harnessed to evaluate the prognostic value of the RPGI. Results A 22-gene RPGI signature was developed, and its risk score served as a strong independent prognostic factor across all data sets when adjusted for major clinical variables. Moreover, ASEs for certain genes, such asFGFR1and theRASoncogene family, were significantly correlated with RPGI. Expression levels of genes involved in splicing- and tumour-associated pathways were significantly correlated with RPGI score. Furthermore, a combination of RPGI with age and tumour stage resulted in significantly improved prognostic accuracy. Conclusions Our findings highlighted the prognostic value of RPGs for risk stratification of CRC patients and provide insights into specific ASEs associated with the development of CRC.
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页数:13
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