Identification of super enhancer-associated key genes for prognosis of germinal center B-cell type diffuse large B-cell lymphoma by integrated analysis

Abstract Background The pathogenesis of germinal center B-cell type diffuse large B-cell lymphoma (GCB-DLBCL) is not fully elucidated. This study aims to explore the regulation of super enhancers (SEs) on GCB-DLBCL by identifying specific SE-target gene. Methods Weighted gene co-expression network a...

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Main Authors: Xi Li (Author), Yan Duan (Author), Yuxia Hao (Author)
Format: Book
Published: BMC, 2021-03-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Xi Li  |e author 
700 1 0 |a Yan Duan  |e author 
700 1 0 |a Yuxia Hao  |e author 
245 0 0 |a Identification of super enhancer-associated key genes for prognosis of germinal center B-cell type diffuse large B-cell lymphoma by integrated analysis 
260 |b BMC,   |c 2021-03-01T00:00:00Z. 
500 |a 10.1186/s12920-021-00916-z 
500 |a 1755-8794 
520 |a Abstract Background The pathogenesis of germinal center B-cell type diffuse large B-cell lymphoma (GCB-DLBCL) is not fully elucidated. This study aims to explore the regulation of super enhancers (SEs) on GCB-DLBCL by identifying specific SE-target gene. Methods Weighted gene co-expression network analysis (WGCNA) was used to screen modules associated with GCB subtype. Functional analysis was performed by gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment. H3K27ac peaks were used to identify SEs. Overall survival analysis was performed using Kaplan-Meier curve with log-rank and Breslow test. The effect of ADNP, ANKRD28 and RTN4IP1 knockdown on Karpas 422 and SUDHL-4 cells proliferation was analyzed by CCK-8. Karpas 422 and SUDHL-4 cells were treated with bromodomain and extra-terminal domain (BET) inhibitor JQ1, and the expression of ADNP, ANKRD28 and RTN4IP1was measured by qRT-PCR. Results A total of 26 modules were screened in DLBCL. Turquoise module was closely related to GCB-DLBCL, and its eigengenes were mainly related to autophagy. There were 971 SEs in Karpas 422 cell and 1088 SEs in SUDHL-4 cell. Function of the nearest genes of overall SEs were related to cancer. Six SE-related genes associated with GCB-DLBCL were identified as prognostic markers. Knockdown of ADNP, ANKRD28 and RTN4IP1 inhibited the proliferation of Karpas 422 and SUDHL-4 cells. JQ1 treatment suppressed ADNP, ANKRD28 and RTN4IP1 expression in Karpas 422 and SUDHL-4 cells. Conclusions A total of 6 SE-related genes associated with GCB-DLBCL overall survival were identified in this study. These results will serve as a theoretical basis for further study of gene regulation and function of GCB-DLBCL. 
546 |a EN 
690 |a Diffuse large B-cell lymphoma 
690 |a Germinal center B-cell type 
690 |a Super enhancers 
690 |a Weighted gene co-expression network analysis 
690 |a Overall survival 
690 |a Internal medicine 
690 |a RC31-1245 
690 |a Genetics 
690 |a QH426-470 
655 7 |a article  |2 local 
786 0 |n BMC Medical Genomics, Vol 14, Iss 1, Pp 1-14 (2021) 
787 0 |n https://doi.org/10.1186/s12920-021-00916-z 
787 0 |n https://doaj.org/toc/1755-8794 
856 4 1 |u https://doaj.org/article/e7c4db9fa1c843f28c3a0931523b64dc  |z Connect to this object online.