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Subasumstat (Synonyms: TAK-981)

Catalog No.GC64972 Copy One-Click Copy Product Info

Subasumstat is a selective inhibitor of the SUMOylation enzyme cascade with potent anti-leukemic activity.

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Subasumstat Chemical Structure

Cas No.: 1858276-04-6

Size Price Stock Qty
10mM (in 1mL DMSO)
$229.00
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1mg
$53.00
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5mg
$149.00
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10mg
$279.00
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50mg
$855.00
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100mg
$1,485.00
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Sample solution is provided at 25 µL, 10mM.



Description of Subasumstat

Subasumstat is a selective inhibitor of the SUMOylation enzyme cascade with potent anti-leukemic activity[1]. SUMOylation is a reversible post-translational modification that is involved in the regulation of multiple cellular processes, including inflammatory responses and type 1 interferon (IFN1) expression[2]. Subasumstat can induce the expression of natural killer cell (NK cell) ligands on acute myeloid leukemia cells and activate NK cell cytotoxicity[3].

In vitro, treatment of human NK cells with Subasumstat (1μM) for 24h significantly increased the intracellular mRNA expression of interferon-γ-induced protein 10 (IP-10) and cluster of differentiation 69 (CD69)[4]. Subasumstat (1μM) treatment of T cells from patients with chronic lymphocytic leukemia (CLL) significantly reduced regulatory T cell (Treg) differentiation and induced IFNγ secretion by CD4+ and CD8+ T cells[5].

In vivo, Subasumstat (15mg/kg) was treated intravenously in THP-1 xenograft mice, which significantly inhibited tumor progression in mice, prolonged the survival of mice, and exerted a synergistic effect with 5-azacytidine (AZA)[6]. Subasumstat (25mg/kg) was treated intravenously in multiple myeloma (MM) cell xenograft mice for 7 days, which significantly inhibited tumor growth and induced apoptosis of primary MM cells[7].

References:
[1] Kotani H, Oshima H, Boucher J C, et al. Dual inhibition of SUMOylation and MEK conquers MYC-expressing KRAS-mutant cancers by accumulating DNA damage[J]. Journal of Biomedical Science, 2024, 31(1): 68.
[2] Du L, Liu W, Rosen S T, et al. Mechanism of SUMOylation-mediated regulation of type I IFN expression[J]. Journal of Molecular Biology, 2023, 435(5): 167968.
[3] Hallal R, De Toledo M, Tempe D, et al. The SUMOylation inhibitor TAK-981 (Subasumstat) triggers IFN-I-dependent activation of Natural Killer cells against Acute Myeloid Leukemias[J]. bioRxiv, 2024: 2024.02. 19.580882.
[4] Nakamura A, Grossman S, Song K, et al. The SUMOylation inhibitor subasumstat potentiates rituximab activity by IFN1-dependent macrophage and NK cell stimulation[J]. Blood, The Journal of the American Society of Hematology, 2022, 139(18): 2770-2781.
[5] Lam V, Roleder C, Liu T, et al. T cell–intrinsic immunomodulatory effects of TAK-981 (subasumstat), a SUMO-activating enzyme inhibitor, in chronic lymphocytic leukemia[J]. Molecular cancer therapeutics, 2023, 22(9): 1040-1051.
[6] Gabellier L, De Toledo M, Chakraborty M, et al. SUMOylation inhibitor TAK-981 (subasumstat) synergizes with 5-azacytidine in preclinical models of acute myeloid leukemia[J]. Haematologica, 2023, 109(1): 98.
[7] Heynen G J J E, Baumgartner F, Heider M, et al. SUMOylation inhibition overcomes proteasome inhibitor resistance in multiple myeloma[J]. Blood Advances, 2023, 7(4): 469-481.

Protocol of Subasumstat

Cell experiment [1]:

Cell lines

Human NK cells

Preparation Method

Human NK cells were treated with 20μg/mL AIFNAR2- and/or 1μM Subasumstat for 24h, and the mRNA expression of IP-10 and CD69 was analyzed by Western blot.

Reaction Conditions

1μM; 24h

Applications

Subasumstat treatment of NK cells resulted in a robust increase in IP-10 and CD69 expression without a significant impact on cell viability.

Animal experiment [2]:

Animal models

NSG mice

Preparation Method

NSG mice were injected with THP-1 cells and treated with Subasumstat (15mg/kg, i.v.), 5-azacytidine (AZA) (2mg/kg, i.p.) or the combination. Quantification, as relative luminescence units, of tumor burden evolution monitored by luminescence intensity in mice injected with bioluminescent THP-1 cells. Overall survival after treatment start of mice injected with bioluminescent THP-1 cells was estimated in each group and compared using Kaplan-Meier method and log-rank test.

Dosage form

15mg/kg; i.v.

Applications

Subasumstat and AZA monotherapy limited tumor progression in THP-1 and significantly prolonged the survival of mice. The combination of Subasumstat+AZA had a higher anti-leukemic effect than monotherapy.

References:
[1]Nakamura A, Grossman S, Song K, et al. The SUMOylation inhibitor subasumstat potentiates rituximab activity by IFN1-dependent macrophage and NK cell stimulation[J]. Blood, The Journal of the American Society of Hematology, 2022, 139(18): 2770-2781.
[2]Gabellier L, De Toledo M, Chakraborty M, et al. SUMOylation inhibitor TAK-981 (subasumstat) synergizes with 5-azacytidine in preclinical models of acute myeloid leukemia[J]. Haematologica, 2023, 109(1): 98.

Chemical Properties of Subasumstat

Cas No. 1858276-04-6 SDF
Synonyms TAK-981
Formula C25H28ClN5O5S2 M.Wt 578.1
Solubility DMSO : 16.67 mg/mL (28.84 mM; ultrasonic and warming and heat to 80°C) Storage Store at -20°C
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of Subasumstat

Prepare stock solution
1 mg 5 mg 10 mg
1 mM 1.7298 mL 8.649 mL 17.298 mL
5 mM 346 μL 1.7298 mL 3.4596 mL
10 mM 173 μL 864.9 μL 1.7298 mL
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Average Rating: 5 ★★★★★ (Based on Reviews and 30 reference(s) in Google Scholar.)

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