Figure 1
Figure 1. Transcriptomic landscapes of CBF and RUNX1-CBFA2T3 AML. (A) Characteristics of CBF and non-CBF AML cohorts. (B-C) Comparative analyses of expressed genes in t(8;21) (B) and inv(16) (C) AML subgroups. Diamonds correspond to differentially expressed genes (difference ≥1 or ≤−1) listed in supplemental Tables 1 and 2 for panels B and C, respectively. Scales: mean{log10[(RPKM+0.0001)*10 000]}. (D) PCA performed in the Leucegene cohort (n = 415) using the 145-gene signature that characterizes AML with t(8;21)/RUNX1-RUNX1T1 (red dots). One sample with a t(16;21)/RUNX1-CBFA2T3 (lime green dot) clustered with t(8;21) AML. (E) PCA performed in the same cohort using the 127-gene signature that characterizes AML with inv(16)/CBFB-MYH11 (steel blue dots). A small constant of 0.0001 was added to all RPKM values prior to log10 transformation. FAB, French-American-British; RPKM, reads per kilobase per million mapped reads; T-AML, therapy-related AML; WBC, white blood cell.

Transcriptomic landscapes of CBF and RUNX1-CBFA2T3 AML. (A) Characteristics of CBF and non-CBF AML cohorts. (B-C) Comparative analyses of expressed genes in t(8;21) (B) and inv(16) (C) AML subgroups. Diamonds correspond to differentially expressed genes (difference ≥1 or ≤−1) listed in supplemental Tables 1 and 2 for panels B and C, respectively. Scales: mean{log10[(RPKM+0.0001)*10 000]}. (D) PCA performed in the Leucegene cohort (n = 415) using the 145-gene signature that characterizes AML with t(8;21)/RUNX1-RUNX1T1 (red dots). One sample with a t(16;21)/RUNX1-CBFA2T3 (lime green dot) clustered with t(8;21) AML. (E) PCA performed in the same cohort using the 127-gene signature that characterizes AML with inv(16)/CBFB-MYH11 (steel blue dots). A small constant of 0.0001 was added to all RPKM values prior to log10 transformation. FAB, French-American-British; RPKM, reads per kilobase per million mapped reads; T-AML, therapy-related AML; WBC, white blood cell.

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