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. 2014 Mar 17;25(3):366-78.
doi: 10.1016/j.ccr.2014.01.032. Epub 2014 Mar 6.

Clonal evolution enhances leukemia-propagating cell frequency in T cell acute lymphoblastic leukemia through Akt/mTORC1 pathway activation

Jessica S Blackburn  1 , Sali Liu  2 , Jayme L Wilder  3 , Kimberly P Dobrinski  4 , Riadh Lobbardi  1 , Finola E Moore  1 , Sarah A Martinez  5 , Eleanor Y Chen  6 , Charles Lee  7 , David M Langenau  8
Affiliations

Clonal evolution enhances leukemia-propagating cell frequency in T cell acute lymphoblastic leukemia through Akt/mTORC1 pathway activation

Jessica S Blackburn et al. Cancer Cell. .

Abstract

Clonal evolution and intratumoral heterogeneity drive cancer progression through unknown molecular mechanisms. To address this issue, functional differences between single T cell acute lymphoblastic leukemia (T-ALL) clones were assessed using a zebrafish transgenic model. Functional variation was observed within individual clones, with a minority of clones enhancing growth rate and leukemia-propagating potential with time. Akt pathway activation was acquired in a subset of these evolved clones, which increased the number of leukemia-propagating cells through activating mTORC1, elevated growth rate likely by stabilizing the Myc protein, and rendered cells resistant to dexamethasone, which was reversed by combined treatment with an Akt inhibitor. Thus, T-ALL clones spontaneously and continuously evolve to drive leukemia progression even in the absence of therapy-induced selection.

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Figures

Figure 1
Figure 1. Clonal evolution drives intratumoral heterogeneity and can lead to increased leukemia propagating frequency
(A) A schematic of the cell transplantation screen designed to identify phenotypic differences between single leukemic clones. (B, C) Schematic of results from primary T-ALL #1 (B) and T-ALL #9 (C). * denotes a significant reduction in LPC frequency from monoclonal primary to secondary transplant (p=0.02). ** denote a significant reduction in LPC frequency from monoclonal primary transplant T-ALL compared with tertiary transplanted leukemia (p<0.0001). Clones are color-coded based on tcrβ-rearrangements. See also Figures S1 and Table S1.
Figure 2
Figure 2. Mechanisms that drive leukemia propagating cell frequency and latency can evolve independently
(A) Fish were transplanted with 25 LPCs from various clones and assessed for time to leukemia onset (n=8-10 animals transplanted per individual clone). * denotes significant differences in latency between clones that have low (upper left panel) or high (lower left panel) LPC frequencies (<0.001). Representative fluorescent images of animals following 28 days of engraftment are shown. (B) Correlation between LPC frequency and T-ALL latency across all clones. (C) EDU analysis of selected clones and correlation with LPC frequency and latency. Each datum point represents a single clone. NS=not significant. ** denote a significant difference in the percent of cells that are EDU-positive (p=0.0004). (D) Animals were transplanted with 25 LPCs from clone 11.2 (dsRED-positive, 1:78 LPC frequency, 88 days latency) and 25 LPCs from clone 4.3 (GFP-positive, 1:246 LPC frequency, 28 days latency). Representative images of whole fish and confocal images of T-ALL cells harvested at 15 days and 45 days post-transplantation. The percentages of dsRED-positive and GFP-positive cells at 15 days and 45 days were analyzed by FACS. Data are represented as ± SE (n= 4-7 transplant recipients per time-point). (E) 25 LPCs from clone 1.3 (zsYellow-positive, 1:13 LPC frequency, 58 days latency) were competed with 25 LPCs from clone 5.1 (amCyan-positive, 1:184 LPC frequency, 30 days latency), and analyzed as in (D). Scale bars, 5 mm in images of whole fish and 40 μm in confocal images. See also Figure S2.
Figure 3
Figure 3. LPC frequency and latency are regulated cell-autonomously in T-ALL
(A) Schematic of the experimental design. (B) Summary of results with 95% confidence intervals shown in parenthesis. § indicates an independent limiting dilution cell transplantation experiment confirming similar results as those shown in Table S1. (C) Kaplan Meier analyses of leukemia re-growth in animals transplanted with individual clones alone or following mixing. Tumor-negative animals were excluded from analysis. See also Figure S3.
Figure 4
Figure 4. Akt pathway activation is acquired by a subset of cells following clonal evolution and drives elevated LPC frequency and growth
(A) Graphical summary of pAkt(S473) IHC from 46 monoclonal T-ALL. Green denotes samples that are pAkt-positive, and black have low or absent pAkt staining. Triangles represent clones that were confirmed for pAkt status by Western blot analysis. The vertical dotted line demarcates clones with short (<45 days) or long latencies, and the horizontal dotted line identifies clones with low (<1.0%) or high LPC frequency. pAkt-positivity is significantly associated with high LPC frequency (p<0.0001) and short latency (p=0.017), by Fisher Exact Test. (B) IHC analysis of pAkt staining in T-ALL clones. Scale bar, 50 μm. (C) Western blot analysis of selected clones from (B). (D) Animals were transplanted with the clones indicated and treated with MK2206 or DMSO for 5 days. Representative images at 28 days post-transplantation with LPC frequencies noted. * denotes a significant change in LPC frequency following MK2206 treatment (p<0.001). Scale bar, 5 mm. (E-G) Kaplan-Meier analyses for T-ALL regrowth following DMSO or MK2206 treatment for clone 2.2 (E), primary monoclonal transplant clone 10.1 (F), and tertiatry transplant clone 10.1 (G). ** denotes a significant change in T-ALL latency following MK2206 treatment (p<0.0001). See also Figure S4 and Table S2-S3.
Figure 5
Figure 5. The Akt pathway increases LPC frequency through downstream activation of mTORC1 and shortens latency by augmenting Myc stability
(A) Representative images of zebrafish that were transplanted with 25 LPCs from T-ALL expressing GFP and the indicated constructs (3 T-ALL per genotype, n=35 animals transplanted per primary leukemia) at 28 days post-transplantation. (B) Kaplan-Meier analyses of time to T-ALL regrowth for each genotype and compared to Myc alone expressing T-ALL. * denotes a significant difference in latency of p<0.0001, and ** indicate a significant difference in latency of p=0.003. (C) EDU analysis of transgenic T-ALL. Each datum point represents the percent EDU-positive cells for one T-ALL. § represents a significant difference of p<0.0001 and §§ denote a significant difference of p=0.004, when compared to Myc alone expressing T-ALL. (D) Graph showing LPC frequency within each transgenic group. Each point represents data for one primary T-ALL. # denotes a significant difference in LPC frequency of p<0.0001 and ## indicate a significant difference in LPC frequency of p=0.0025 when compared to Myc alone expressing T-ALL. NS denotes no significant difference. (E) Western blot analysis. See also Figure S5 and Table S4.
Figure 6
Figure 6. Dexamethasone resistance is acquired following Akt pathway activation in clonally evolved cells and can be overcome by combined treatment with MK2206
(A) Primary monoclonal T-ALL that were pAkt-negative (red) and tertiary transplanted T-ALL that were pAkt-positive (green) were treated ex vivo as indicated and assessed for viability (n=6 replicates per clone). Error bars are ± SE. (B) Human cell lines with (green) or without (red) active Akt signaling were treated in vitro as indicated. Each point is the average viability after 24 hr of drug treatment (n=3 replicates per cell line). Error bars ± SE. (C) Representative images of leukemic fish prior to or 4 days after drug treatment with DMSO, 350 mg/L Dexamethasone, 3.5 μM MK2206 or 350 mg/L Dexamethasone+3.5 μM MK2206. Clone name and pAkt status are shown to the left. Waterfall plots at the bottom summarize the in vivo T-ALL responses. Each bar denotes the percent change in T-ALL burden within a single animal, those with diagonal lines indicate >50% reduction in T-ALL burden. See also Figure S6.
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Comment in

  • Leukemia propagating cells Akt up.
    Gutierrez A, Roderick JE, Kelliher MA. Gutierrez A, et al. Cancer Cell. 2014 Mar 17;25(3):263-5. doi: 10.1016/j.ccr.2014.02.022. Cancer Cell. 2014. PMID: 24651006

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