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HA22 (Moxetumomab pasudotox) is a recombinant immunotoxin (RIT), composed of an anti-CD22 Fv fused to a truncated portion of Pseudomonas exotoxin A. HA22 is in clinical trials to treat patients with hairy cell leukemia and acute lymphoblastic leukemia (ALL). LMB-11 is an improved variant of HA22 with reduced immunogenicity, has a longer half-life in the blood and high activity in vitro and in a Burkitt lymphoma model in vivo. Searching for RIT enhancing combination therapies, we found the protein kinase A inhibitor H89 to enhance LMB-11 and HA22 activity 5- to 10-fold on ALL cell lines and on patient-derived ALL samples. In addition, H89 increased the activity of mesothelin-targeting RITs SS1P (38-fold) and RG7787 (7-fold) against the cervical cancer cell line KB31. Unexpectedly we found that the enhancement by H89 was not due to inhibition of protein kinase A; it was partially recapitulated by inhibition of S6K1, which led to inactivation of its down-stream targets rpS6 and GSK3β, resulting in a fall in MCL1 levels. H89 increased the rate of ADP-ribosylation of eukaryotic elongation factor 2, enhancing the arrest of protein synthesis and the reduction of MCL1 in synergy with the RIT. In summary, H89 increased RIT activity by enhancing the two key events: ADP-ribosylation of eEF2 and reduction of MCL1 levels. Significant enhancement was seen with both CD22- and mesothelin-targeting RITs, indicating that H89 might be a potent addition to RIT treatment of CD22-positive ALL and mesothelin-expressing solid tumors.
Acute lymphoblastic leukemia (ALL) is the most common childhood cancer (1). Current treatment regimens result in 80% long-term survival (2); however, disease relapse is associated with a poor outcome (3) and ALL remains the leading cause of cancer-related deaths in children and young adults (2, 4). To further improve response rates, novel treatment options have been developed which are currently in clinical evaluation (5–10).
As part of the effort to find new ALL therapeutics, we generated Pseudomonas exotoxin A (PE)-derived recombinant immunotoxins (RITs). To do this, the binding domain of the toxin is replaced with an FV portion of a monoclonal antibody, which is chosen to target cancer cells, but not normal essential tissues (11, 12). For targeting B-ALL and other B cell malignancies, CD22 is a favorable target molecule (13, 14). HA22 (also known as CAT-8015 or Moxetumomab pasudotox (15)) is a CD22-targeting RIT in which an anti-CD22 FV is fused to a 38 kDa fragment of PE. HA22 produced complete remissions in nearly 50% of patients with drug resistant HCL (15) and in 24% of children with chemotherapy-refractory ALL (5, 16). In attempt to improve the activity of CD22-targeting RITs, we developed LMB-11 in which the Fv was replaced with an Fab, and immunogenicity was reduced by deleting most of domain II and modifying seven B-cell epitopes in domain III (17). LMB-11 is more active than HA22 in a CA46 Burkitt lymphoma animal model, where it produced complete regressions of tumors (18).
The mechanism by which RITs kill cells is complex and not completely understood. After binding to the surface receptor and internalization, RITs are cleaved by furin and traverse cells through various endocytic compartments using retrograde trafficking to reach the endoplasmic reticulum and ultimately the cytosol. There, PE catalyzes ADP-ribosylation of eukaryotic elongation factor 2 (eEF2), which arrests protein synthesis and leads to apoptosis (5, 12, 19).
Protein kinases play an essential role in all aspects of signal transduction pathways involving cell growth, proliferation, metabolism, and disease. Similarly, protein kinases also modulate how effectively RITs traverse the various cellular compartments. We showed that small GTPases ARF1 and ARF4 are involved in the regulation of RIT trafficking (20) and have identified the insulin receptor (21) and the Src-family kinase HCK (22) as important modulators of the activity of HA22 as well as the mesothelin-targeting RIT SS1P. Protein kinase A (PKA) has been implicated in numerous cellular processes. The study of PKA function has been dominated by the use of pharmacological inhibitors. One of these, H89, is a strong PKA inhibitor with the ability to readily cross the cell membrane, with pre-clinical activity demonstrated in vitro and in vivo (23–26).
Here, we show that H89 strongly enhances the activity of the CD22 targeting RITs LMB-11 and HA22 on ALL cell lines and patient-derived ALL cells and of a mesothelin-targeting RIT on a cervical cancer cell line. The strong enhancement is due to more efficient ADP-ribosylation of eEF2 by RIT in combination with a synergistic reduction of MCL1 by the two drugs in combination.
HA22 (27), LMB-11 (18), LMB-31 and SS1P (28, 29) were purified as described (30). Immunotoxin LMB-31, an inactive form of LMB-11, was generated by site directed mutagenesis changing E553 to D553 in the PE fragment. RG7787 (huSS1(Fab)-LR-GGS-LO10-PE24) was supplied by Roche Innovation Center Penzberg, Germany under a Cooperative Research and Development Agreement (31).
Antibodies detecting p-S6K1(T389), S6K1, p-CREB(S133)/ATF-1, p-rpS6(S240/244), rpS6, p-GSK3β (S9), GSK3β, Bcl2, PARP, cleaved caspase 3, Bax, Bcl-xL, and MCL1 were purchased from Cell Signaling (Danvers, MA); H89 from Selleck (Houston, TX); 8-Br-cAMP, Dibutyl-cAMP and anti-β-Tubulin from Sigma (St. Louis, MO); anti-Actin from Abcam (Cambridge, MA); and inhibitors PKI-myristoylated (14–22) amide and S6K1 inhibitor PF4708671 from Tocris Sciences (Pittsburgh, PA).
Human ALL cell lines HAL-01, KOPN-8, REH, SEM, NALM-6, and cervical cancer cell line KB31 were cultured in RPMI and supplemented with 10% fetal bovine serum and 1% penicillin-streptomycin at 37°C. The cell lines HAL-01 (32), NALM-6 (9) and KB31 (21) cells were described previously. KOPN-8 and SEM cells were purchased from DSMZ (Germany); REH was obtained from ATCC. All the cell lines identities were confirmed by short tandem repeat analysis at the Frederick National Laboratory for Cancer Research in 2012 or 2013. The cells were then frozen in aliquots and thawed as needed.
Cytotoxic activity of RITs in combination with inhibitors was determined by growth inhibition assays as described (18). Briefly, 10,000 ALL cells or 5,000 KB31 cells were plated per well in a 96 well format. Treatment was added to the wells 5 hours after plating. Inhibitor or vehicle was added first for 1 hour or as indicated, followed by RIT or 100 μg/ml Cycloheximid for positive control. After 72 hours of incubation, WST8 was added. Resulting OD450-values were normalized to Cycloheximid and medium control.
Cells were washed in phosphate buffered saline (PBS) and lysed for 30 minutes on ice in modified RIPA buffer (50 mM Tris HCl, 150 mM NaCl, 5 mM EDTA, 1% NP40, 5 μg/ml leupeptin, 5 μg/ml aprotinin, 10 μM PMSF). After high-speed centrifugation, supernatants were analyzed by SDS-PAGE, transferred to PVDF membranes, and subjected to western blot analysis.
Internalization of LMB-11 was measured as described (33). Briefly, KOPN-8 cells were treated with or without 10 μM H89 for 1 hour in 6-well plates, 1 μg/ml of LMB-11-Alexa647 was added and cells were incubated at 37°C for the indicated times. Cells were washed with PBS and stripped 10 minutes with 0.2 M Glycine-HCl (pH2.5) to remove surface bound LMB-11, washed with FACS buffer (PBS with 5% FBS, 0.1% NaN3) and analyzed by flow cytometry using a FACS Calibur (Becton Dickinson, Franklin Lakes, NJ).
The rate of furin-cleavage was determined as described (21). KOPN-8 cells were treated with 10 μM H89 or vehicle for 1 hour. One μg/ml of HA22 was added and cells incubated on ice for 30 minutes to saturate HA22 binding. Cells were washed, medium changed, and incubated at 37°C for the indicated times before cell lysis and western blot analysis.
Cells were lysed in modified RIPA buffer; 5 μg protein from the cell lysates was incubated with 50 ng LMB-11 in ADP-ribosylation buffer (20 mM Tris-HCl (pH 7.4), 1 mM EDTA, 50 mM DTT) with 0.3 μM of 6-biotin-17-NAD (Trevigen, Gaithersburg, MD) for 60 min at 25°C. Samples were subjected to SDS-PAGE, followed by western blotting with HRP-conjugated streptavidin to detect biotin-ADP-ribose-eEF2.
Protein synthesis inhibition was performed using a 3H-leucine incorporation assay as described (30). 5,000 KOPN-8 cells were plated per well of a 96 well plate with 10 μM H89 or vehicle and treated with various concentrations of LMB-11. After 16 hours, wells were pulsed with 2 μCi 3H-Leucine for 2 hours at 37°C. Plates were harvested for readout using a liquid scintillation counter (Wallac, Wellesely, MA).
KOPN-8 cells in 6 well plates were treated with LMB-11 in combination with 10 μM H89 or vehicle for indicated times. Cells were harvested and stained with Annexin V-PE and 7-AAD according to kit instructions (BD Biosciences, San Jose, CA). Cells were run on a FACS Calibur and data analyzed in FlowJo (Tree Star Inc, San Carlos, CA).
Primary ALL blast samples were collected from four patients with CD22 positive pre-BALL under protocols approved by the NCI Institutional Review Board. Samples that had been viably cryopreserved and stored in liquid nitrogen were thawed, washed, resuspended in PBS and injected IV in immunodeficient (NSG) mice. Mice were euthanized at disease progression, and whole spleen and bone marrow extracted (spine, hip, and femur by crushing with mortar and pestle). Cells were analyzed by flow for hu-CD19, hu-CD22, and hu-CD10, and viably frozen in RPMI-1640 containing 10% DMSO and stored in liquid nitrogen. All animals were handled according to the National Institutes of Health guidelines and studies were approved by the Animal Care and Use Committee of the NCI.
For apoptosis studies, 300,000 cells were plated in α-MEM media containing 20% FBS in a 96-well format. The cells were treated with 15 μM H89 for 30 min after which HA22 or LMB-11 was added. After 72 hours, cells were harvested, stained with anti-human-CD19-FITC, Annexin V-PE, and 7-AAD. The CD19 positive population was defined as ALL cells, of which the % living cells was determined as double negative for Annexin V-PE and 7-AAD. Results were analyzed in Prism Graph and all values were normalized to only vehicle treated sample.
Figure 1 shows that H89 greatly increased the activity of CD22-targeting RITs. The IC50 of LMB-11 on KOPN-8 was enhanced 9-fold from 1.1 ng/ml to 0.13 ng/ml by 10 μM H89 (Fig. 1A). Cytotoxic activity of HA22 was shifted from 0.08 ng/ml to 0.03 ng/ml (Fig. 1B). To test if the enhancing effect of CD22-RITs was depending on a catalytically active PE, we combined H89 with the inactive LMB-11-E553D mutant LMB-31 (34). Neither LMB-31 alone nor the combination with H89 showed cytotoxic activity (Fig. 1C). To show that the H89 effect was target-dependent, we tested the mesothelin-targeting RIT RG7787. RG7787 had no cytotoxic effect against mesothelin-negative KOPN-8 and there was no increase in RG7787 cytotoxicity by the addition of H89 (Fig. 1D). We also examined the effect of H89 on Cycloheximide, an agent that inhibits protein synthesis by a different mechanism than RITs and found no enhancement (Fig. 1E). H89 itself had minimal inhibitory effects on KOPN-8 growth rate at 2.5 or 5 μM. At 10 μM H89, KOPN-8 cell growth was inhibited 20% (data not shown). These data together indicated that H89 specifically enhanced the activity of CD22-targeted RITs against KOPN-8 cells. We then examined the effects of H89 on four other ALL cell lines, Hal-01, NALM-6, SEM and REH. As shown in Figure 1F, H89 enhanced LMB-11 activity by 3- to 10-fold. The enhancement of H89 on different cell types (IC50) is summarized in Supplementary Table S1.
To investigate the mechanism of cytotoxicity enhancement by H89, we first evaluated the internalization rate of Alexa647-labeled LMB-11. Figure 2A shows that the amount of internalized LMB-11-Alexa647 over time was the same for H89 or vehicle treated KOPN-8. After RIT internalization, the protease furin cleaves PE between residues 279 and 280 which liberates the catalytically active 35 kDa PE fragment from the antibody moiety (19). Because LMB-11 was de-immunized by removing B-cell epitopes (17), antibodies against PE recognize this immunotoxin and its cleaved fragment very weakly, and thus cannot be used to detect the cleaved product of LMB-11. However, our antibodies bind strongly to the wild-type HA22. Because the rate of internalization was similar for Alexa647-labeled HA22 or LMB-11 and enhancement of their cytotoxic activity by H89 was comparable, we measured changes in the rate of furin-cleavage for HA22. As shown in Figure 2B, the cleaved 35 kDa fragment became detectable after 30 minutes and increased up to 2 hours. There was no difference between control and H89 treated samples in the rate of furin cleavage.
We next evaluated if H89 enhanced the ability of RIT to arrest protein synthesis in KOPN-8 cells. We measured the rate of 3H-Leucine incorporation after cells were treated with LMB-11 with or without H89 and found that arrest of protein synthesis was enhanced 10-fold by H89 (Fig. 2C); H89 itself did not inhibit protein synthesis in KOPN-8 (Fig. 2C).
Because protein synthesis arrest by RIT is a result of ADP-ribosylation of eEF2, we determined if the increased arrest of protein synthesis by H89 correlated with an increase in the level of eEF2-ADP-ribose. KOPN-8 cells were incubated with LMB-11 and 10 μM H89 or vehicle for up to 10 hours. Cell lysates were prepared at various times and the cell extract treated with biotinylated NAD and RIT to ADP-ribosylate unmodified eEF2. In untreated cells, eEF2 is not ADP-ribosylated, so RIT added biotin-ADP-ribose maximally on eEF2 in the cell free reaction. Figure 3A shows that in cells treated with LMB-11 alone, the level of ADP-eEF2 fell slowly and even after 10 hours of treatment, 20% of the eEF2 could still be modified with biotin-ADP-ribose. In cells treated with H89 and LMB-11, there was a very rapid fall in the amount of eEF2 that could be ADP-ribosylated. The signal for biotin-ADP-ribose was undetectable from 8 hours with the combination (Fig. 3A). This increase in ADP-ribosylation corresponded to the increased arrest of protein synthesis (Fig. 2C). To assess whether the H89-effect was observed with another cell line, we examined LMB-11 treated SEM cells and found that H89 similarly increased ADP-ribosylation of eEF2 (Supplementary Fig. S1).
As a result of RIT-induced arrest of protein synthesis, MCL1 levels fall, which triggers induction of intrinsic apoptosis (35). As shown in Figure 3A, KOPN-8 cells treated with LMB-11 alone showed a reduction of MCL1 levels after 10 hours. With the addition of H89, the level of MCL1 fell very rapidly below the detection limit after only 4 hours. Accordingly, cleaved PARP was detected earlier with combination treatment (Fig. 3A). Because high doses of LMB-11 (200 ng/ml) with H89 eliminated MCL1 levels, we studied combination treatment using a lower concentration of LMB-11 (5 ng/ml). Each agent alone reduced MCL1 by approximately 50% after 24 hours, and when combined, MCL1 was no longer detectable (Supplementary Fig. S2A). Levels of other apoptosis regulating proteins such as Bcl2, Bax and Bak did not change within 24 hours.
The experiments described above measure early and intermediate events in RIT action, but do not measure cell death. To ensure that the changes in biochemical events studied ultimately resulted in an earlier and higher rate of apoptosis, we quantified cell death after 24 or 48 hours of treatment using flow cytometry. Figure 3B shows that 3 or 6 ng/ml LMB-11 alone had little effect on KOPN-8 after 24 hours of treatment. But at 48 hours there was 50% death with 3 ng/ml and 75% with 6 ng/ml. When 10 μM H89 was added to LMB-11, significant cell death was observed after 24 hours and most cells were dead at 48 hours. H89 itself did not induce any cell death up to 48 hr.
We next investigated which of the H89 targets was responsible for the observed enhancing effects. H89 has been developed as PKA inhibitor, but it also inhibits other kinases (36). We tested if other PKA regulators would modulate RIT activity. To our surprise, the addition of a more specific PKA inhibitor, PKI, did not enhance LMB-11 (Fig. 4A). Furthermore, the PKA activating molecules dibutyryl-cAMP (Fig. 4B), 8-Br-cAMP, or Forskolin (Supplementary Fig. S3A & B) did not decrease the cytotoxic activity of LMB- 11. These data indicate that inhibition of PKA is not likely responsible for the H89-associated increase in LMB-11 activity.
To investigate which kinases besides PKA were inhibited by H89, we screened a panel of 359 protein kinases for H89 inhibitory activity. Supplementary Table S2 shows that H89 inhibited 21 kinases by 90% or more. To examine the relevance of these kinases, we measured RNA levels of the 21 kinases in an internal RNA deep sequencing dataset. The RPKM-values for the 21 kinases from the ALL cells KOPN-8, REH, NALM-6, SEM, and HAL-01 were averaged. We defined the threshold for relevant mRNA levels to be greater than an RPKM of 10 (31). Fourteen of the kinases that were inhibited more than 90% by H89 had an average RPKM above 10. We tested these 14 kinases for their RIT-enhancing activity using pharmacological inhibitors. Two of the 14 kinases partially recapitulated the H89 induced LMB-11 enhancement. p70S6-kinase (S6K1) inhibitor PF4708671 enhanced LMB-11 activity up to 2-fold in a concentration dependent manner and the ROCK2 kinase inhibitor, Stemolecule, also produced a 2-fold enhancement of LMB-11 activity (Supplementary Fig. S3C & D). However, neither of the kinase inhibitors alone or in combination (data not shown) replicated the strong enhancement of LMB-11 by H89 against KOPN-8 cells.
We analyzed the phospho-protein levels of relevant targets by western blot to determine biochemical changes under H89 treatment. As shown in Figure 4C, phospho-CREB and phospho-ATF1, two targets of PKA, underwent only minor changes in cells treated with H89. Vehicle treated cells showed an elevation of the level of S6K1-(T389)-phosphorylation after 15 min which increased further up to 2 hours. With the addition of H89, the p-S6K1-(T389) elevation was largely reduced while total S6K1 remained unaltered. The phosphorylation levels of S6K1 targets rpS6 (ribosomal protein S6) and p-GSK3β fell rapidly within 5 minutes and stayed low (p-GSK3β) or undetectable (p-rpS6) for 120 minutes. The total level of the anti-apoptotic protein MCL1 was decreased 5 minutes after the addition of H89 and remained low for the 2 hour treatment period. In accordance with our inhibitor studies, phosphorylation of PKA targets changed very little which supports our earlier conclusion that PKA-inhibition is not responsible for the enhancement by H89.
To determine if the robust enhancement of cytotoxicity was specific to CD22-targeting RITs, we studied H89 in combination with anti-mesothelin RITs that target epithelial cancers. As shown in Figure 5A, SS1P (28, 29), which is similar in structure to HA22, has an IC50 on KB31 cells of 11 ng/ml, which is lowered 9-fold to1.3 ng/ml by 10 μM H89 and 38-fold to 0.3 ng/ml by 15 μM H89. Similarly, the IC50 of RG7787, an Fab containing mesothelin-targeting RIT the construct of which resembles LMB-11 (31), was reduced from 12 ng/ml to 3 and 1.2 ng/ml by 10 or 15 μM H89, respectively (Fig. 5B).
Because WST8 assays measure mainly cell growth inhibition, we confirmed improved cell killing by H89 using light microscopy. KB31 cells treated with RG7787 at 20 ng/ml or H89 at 15 μM alone were not killed in 3 days. But when H89 and RG7787 at these same concentrations were combined, cells died within 3 days (Fig. 5C). Induction of cell death after treatment with the combination of H89 and RG7787 was also confirmed by flow cytometry after staining with 7-AAD and Annexin V. We also analyzed biochemical changes for the combination treatment against KB31 to confirm the mechanism of action. As seen in KOPN-8, MCL1 was only marginally reduced after 24 hours of treatment with either H89 or RIT alone, but was abolished when the two were combined (Supplementary Fig. S2B). The combination of RIT and H89 was also more potent in inducing PARP-cleavage than either drug alone.
We tested H89 on patient-derived ALL samples to determine if the effects of H89 might be clinically relevant. Because these ALL cells had been propagated through murine xenografts, we used flow cytometry to determine the living cells of the human ALL population for each sample. We treated four patient-derived samples in vitro with immunotoxins HA22 or LMB-11 in combination with H89. H89 greatly enhanced RIT-activity in all four samples (Fig. 6A & B). H89 by itself did not kill patient samples 1, 2, and 4 (all data in Figure 6 were normalized to only vehicle treated cells), but significantly increased both HA22 and LMB-11 killing 3–10 fold. Cells from patient 3 were resistant to both HA22 and LMB-11. When H89 was added, 40% of the cells died within 3 days due to the inhibitor alone. The combination of H89 with either HA22 or LMB-11 resulted in a dose dependent killing of most of the prior RIT-resistant cells.
We show that the protein kinase inhibitor H89 enhances the cytotoxic activity of CD22-targeting immunotoxins LMB-11 and HA22 on ALL cell lines and the cytotoxic activity of mesothelin-targeting RITs SS1P and RG7787 on KB31 cells. Additionally, H89 enhances RIT-induced cell killing on patient-derived ALL cells, which supports the clinical relevance of these findings. We demonstrated the H89 effect to be dependent on a catalytically active PE and specific for PE-induced arrest of protein synthesis on eEF2. Cell death produced by Cycloheximide, a protein synthesis inhibitor that has a different mechanism of action, was not enhanced by H89. H89 activity was partially recapitulated by inhibition of S6K1, resulting in a fall in MCL1. This S6K1 induced reduction of MCL1 worked together with the fall in MCL1 due to arrest of protein synthesis by RIT, ultimately increasing apoptosis.
H89 was developed as a competitive inhibitor for ATP-binding to PKA. It is now known that H89 also inhibits other kinases such as ROCK2, S6K1, MSK1/2, or RSK (36–38). Our in vitro kinase screen confirmed that H89 not only inhibited these kinases, but also other AGC kinase subfamily members (39) including AKT, PKC, PKN, PKG, LATS, PRKX, and NDR2, as well as kinases unrelated to the AGC subfamily including FAK/PTK2 and ARK5/NUAK1.
Because we found the S6K1 inhibitor PF4708671 was a less potent RIT activator than H89 we tested the biochemical changes produced when it was combined with LMB-11. As expected from the S6K1 inhibition, the combination of PF4708671 with LMB-11 resulted in a rapid fall in MCL1 (Supplementary Fig. S4) similar to the effects of H89. But PF4708671 only slightly enhanced the ADP-ribosylation of eEF2 showing a striking difference between the two S6K1 inhibiting molecules. We interpret this as a possible explanation for the stronger RIT enhancement with H89 than with PF4708671. That none of the tested inhibitors for GSK3β, S6K1, or ROCK2 alone or in combination were able to mimic the enhancement of LMB-11 by H89 suggest that the strong RIT enhancing effects by H89 are based on the inhibition of more than one kinase.
The mechanism by which H89 enhances RIT activity appears to involve at least two major events in RIT-induced cell death, ADP-ribosylation and MCL1 degradation. H89 enhances ADP-ribosylation of eEF2 by RITs, which leads to an enhanced arrest of protein synthesis (5, 12). That H89 did not enhance the catalytically inactive LMB-31 highlights the necessity of ADP-ribosylation as a key event in the cell killing associated with the combination of H89 and LMB-11. Notably, H89 alone did not affect ADP-ribosylation (Fig. 3A, time point 0). Together, these data suggest that a RIT–related process that precedes actual ADP-ribosylation is altered by H89. This could be related to enhanced RIT transport to the endoplasmic reticulum or from the endoplasmic reticulum to the cytosol where eEF2 is located. Following protein synthesis inhibition due to the inactivation of eEF2, protein levels of the PEST-sequence containing MCL1 fall because of its rapid turnover (35).
Although H89 alone did not itself arrest protein synthesis, we observed that it had several effects of its own on cells. H89 reduced the phosphorylation of rpS6(240/244) and abolished p-GSK3β(S9) at their respective S6K1 phosphorylation sites (40). This indicates that the activity of these well-established S6K1 targets is modulated by H89. The reduction of phosphorylation at Ser(9) of GSK3β results in an increase in its kinase activity. GSK3β phosphorylates MCL1 at Ser(159) within the PEST sequence which increases ubiquitination and degradation of MCL1 (41–43). We showed this synergistic decrease of MCL1 for both mesothelin- and CD22-targeting RITs. Of note, the levels of other apoptosis modulators like Bax, Bak, or Bcl2 were not changed; emphasizing the central role of MCL1 in the mechanism of H89 enhanced apoptosis induction by RITs.
MCL1 plays a pivotal role in protecting cells from apoptosis and this protein is overexpressed in many cancers (35, 44–46) including ALL subsets (47). Targeting MCL1 degradation represents an important pharmacological approach in cancer drug development (48). Therefore, the rapid fall of MCL1 with H89 treatment could explain the effective killing of cells from patient 3 that were otherwise RIT-resistant.
H89 strongly enhanced immunotoxin activity against ALL cell lines and patient derived cells as well as against an epithelial cancer cell line in vitro. These data strongly support further pre-clinical development of H89 for combination treatment with Pseudomonas exotoxin A based immunotoxins that target CD22 and mesothelin expressing tumors.
Financial support: The work was supported in part by award number P30CA014089 from the National Cancer Institute, the Intramural Research Program of the NIH, National Cancer Institute, and the Center for Cancer Research, and by a Cooperative Research and Development Agreement (#1975) with MedImmune, LLC. F.Müller was supported in part by the German Research Foundation, award number MU 3619/1-1.
The authors wish to thank Richard Beers for the cloning and expression of LMB-31.
Conflict-of-Interest: A.S.W. and I.P. are co-inventors on patents assigned to the NIH for the investigational products. A.S.W. has received from MedImmune: research support, honorarium, travel support; Pfizer, Kite Pharma, and Spectrum Pharmaceuticals: honorarium and travel support. X.L., F.M., and I.P. declare no financial interests.