The MLLT (Mixed Lineage Leukemia Translocated) family, part of the broader MLL (Mixed Lineage Leukemia) network, plays a crucial role in hematopoiesis and leukemogenesis. Members of the MLLT family, such as MLLT1, MLLT3, and MLLT10, are frequently involved in chromosomal translocations associated with various forms of leukemia, particularly acute lymphoblastic and myeloid leukemias. These translocations often result in the formation of fusion proteins combining MLL with MLLT family proteins, leading to altered gene expression. The MLLT proteins, through these fusions, contribute to the dysregulation of gene transcription, particularly affecting genes involved in cell growth and differentiation. Such dysregulation is primarily mediated by altered histone methylation patterns, as MLLT proteins interact with chromatin-modifying complexes, influencing epigenetic regulation. The critical role of MLLT family signaling in the pathogenesis of leukemia makes it a significant target for developing targeted therapies and understanding cancer biology.
MLLT (Mixed Lineage Leukemia Translocated) family inhibitors are designed to interfere with the aberrant protein-protein interactions and epigenetic modifications induced by MLLT fusion proteins. For example, inhibitors that disrupt the interaction between MLLT fusion proteins and key cofactors like DOT1L or menin can hinder the leukemogenic process by normalizing gene expression patterns. Additionally, targeting the downstream effects of MLLT translocations, such as through histone modification enzymes like HDACs or bromodomain-containing proteins, can also be effective.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
9-[5-Deoxy-5-[[cis-3-[2-[6-(1,1-dimethylethyl)-1H-benzimidazol-2-yl]ethyl]cyclobutyl](1-methylethyl)amino]-β-D-ribofuranosyl]-9H-purin-6-amine | 1380288-87-8 | sc-500607 | 50 mg | $13500.00 | ||
This small molecule inhibitor targets the DOT1L enzyme, which is involved in the regulation of AF-It has been investigated for its potential for MLL-rearranged leukemia. | ||||||
Epz004777 | 1338466-77-5 | sc-507560 | 100 mg | $575.00 | ||
This compound targets the AF10-BRD9 interaction and has been investigated for its anti-leukemic effects. | ||||||
GSK J1 | 1373422-53-7 | sc-391113 sc-391113A | 10 mg 50 mg | $193.00 $813.00 | ||
Although primarily known as a histone demethylase inhibitor, GSK-J1 has been studied for its impact on MLL-AF10 leukemia. | ||||||
UNC1999 | 1431612-23-5 | sc-475314 | 5 mg | $142.00 | 1 | |
This compound is a potent inhibitor of the menin-MLL interaction, which is relevant in MLL-fusion leukemias. | ||||||
(±)-JQ1 | 1268524-69-1 | sc-472932 sc-472932A | 5 mg 25 mg | $231.00 $863.00 | 1 | |
Bromodomain Inhibitors targeting bromodomains that recognize acetylated lysines, these inhibitors can disrupt the chromatin-associated functions of MLL fusion proteins. | ||||||
Panobinostat | 404950-80-7 | sc-208148 | 10 mg | $200.00 | 9 | |
Histone Deacetylase (HDAC) Inhibitors by altering histone acetylation, these compounds can impact the chromatin modifications and gene expression patterns driven by MLLT fusion proteins. | ||||||
PKC-412 | 120685-11-2 | sc-200691 sc-200691A | 1 mg 5 mg | $52.00 $114.00 | 10 | |
FLT3 Inhibitors in cases where FLT3 mutations co-occur with MLL rearrangements, targeting FLT3 can be an effective strategy. | ||||||
R788 | 901119-35-5 | sc-364597 sc-364597A | 2 mg 50 mg | $405.00 $4000.00 | 2 | |
Spleen tyrosine kinase (Syk) can be involved in signaling pathways associated with MLL-rearranged leukemias. | ||||||
Flavopiridol | 146426-40-6 | sc-202157 sc-202157A | 5 mg 25 mg | $78.00 $259.00 | 41 | |
Targeting CDK9 can disrupt transcription elongation, a process crucial for the expression of genes controlled by MLLT fusion proteins. | ||||||