Skip to main content
. 2023 Mar 16;11:31. doi: 10.1186/s40364-023-00461-0

Table 1.

Comparison of significant pathways enriched by DEGs associated with cytogenetic risk in paired bulk MNCs versus VLBs

Cytogenetic-Related Genes in MNCs (N = 392) Cytogenetic-Related Genes in VLBs (N = 455)
Pathway Rank (N = 835) Pathway Name Entities FDR Pathway Rank (N = 1020) Pathway Name Entities FDR
1 Phosphorylation of CD3 and TCR zeta chains 1.09E-11 1 Transcriptional regulation of granulopoiesis 8.70E-05
2 Translocation of ZAP-70 to Immunological synapse 2.46E-11 2 NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport & efflux 0.003861
3 PD-1 signaling 4.86E-11 3 NR1H2 and NR1H3-mediated signaling 0.006610
4 Generation of second messenger molecules 2.46E-09 4 RUNX3 regulates CDKN1A transcription 0.061994
5 Neutrophil degranulation 4.79E-07 13 Neutrophil degranulation 0.450842
6 MHC class II antigen presentation 4.79E-07 53 Cytokine Signaling in Immune system 0.593232
7 Costimulation by the CD28 family 4.94E-07 90 Immune System 0.593232
8 Downstream TCR signaling 6.04E-05 128 Interferon Signaling 0.593232
9 TCR signaling 1.22E-04 359 MHC class II antigen presentation 0.593232
10 Interferon Signaling 7.42E-04 535 Generation of second messenger molecules 0.626337
11 Immune System 7.42E-04 687 Translocation of ZAP-70 to Immunological synapse 0.779539
12 Interferon gamma signaling 0.001212 718 Phosphorylation of CD3 and TCR zeta chains 0.802141
13 Cytokine Signaling in Immune system 0.003510 799 Costimulation by the CD28 family 0.871081
17 RUNX3 regulates CDKN1A transcription 0.107059 828 TCR signaling 0.898506
41 Transcriptional regulation of granulopoiesis 0.500239 991 Interferon gamma signaling 0.998825
55 NR1H2 and NR1H3-mediated signaling 0.557604 Not Identified PD-1 signaling N/A
59 NR1H3 & NR1H2 regulate gene expression linked to cholesterol transport & efflux 0.557604 Not Identified Downstream TCR signaling N/A

The lists of DEGs significantly associated with cytogenetic risk groups from paired bulk MNCs and VLBs were downloaded into Reactome to identify pathways enriched in the lists. Pathways significantly associated with cytogenetic risk in bulked MNCs and VLBs were examined separately. Table shows the significance and rank by FDR of individual pathways that were significant in MNCs and VLBs using the list derived from bulk MNCs (left columns) and VLBs (right columns). Those pathways significant associated with the list of genes from bulk MNCs and VLBs are highlighted in light blue and gold, respectively. The significant pathways identified in the bulk MNCs (N = 13) were not significantly enriched for in the VLBs, and vice versa