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.
产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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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 | ¥152307.00 | ||
这种小分子抑制剂以 DOT1L 酶为靶标,该酶参与 AF-I 的调控,已被研究用于治疗 MLL 重排白血病。 | ||||||
Epz004777 | 1338466-77-5 | sc-507560 | 100 mg | ¥6487.00 | ||
该化合物以 AF10-BRD9 相互作用为靶点,其抗白血病作用已得到研究。 | ||||||
GSK J1 | 1373422-53-7 | sc-391113 sc-391113A | 10 mg 50 mg | ¥2132.00 ¥8992.00 | ||
虽然 GSK-J1 主要是一种组蛋白去甲基化酶抑制剂,但也有人研究过它对 MLL-AF10 白血病的影响。 | ||||||
UNC1999 | 1431612-23-5 | sc-475314 | 5 mg | ¥1602.00 | 1 | |
该化合物是 Menin-MLL 相互作用的强效抑制剂,与 MLL 融合型白血病有关。 | ||||||
(±)-JQ1 | 1268524-69-1 | sc-472932 sc-472932A | 5 mg 25 mg | ¥2550.00 ¥9545.00 | 1 | |
溴结构域 抑制剂靶向识别乙酰化赖氨酸的溴结构域,这些抑制剂可破坏 MLL 融合蛋白的染色质相关功能。 | ||||||
Panobinostat | 404950-80-7 | sc-208148 | 10 mg | ¥2211.00 | 9 | |
组蛋白去乙酰化酶(HDAC)抑制剂通过改变组蛋白乙酰化,这些化合物可以影响染色质修饰和由 MLLT 融合蛋白驱动的基因表达模式。 | ||||||
PKC-412 | 120685-11-2 | sc-200691 sc-200691A | 1 mg 5 mg | ¥575.00 ¥1264.00 | 10 | |
FLT3 抑制剂 在 FLT3 突变与 MLL 重排同时出现的病例中,靶向 FLT3 是一种有效的策略。 | ||||||
R788 | 901119-35-5 | sc-364597 sc-364597A | 2 mg 50 mg | ¥4569.00 ¥45128.00 | 2 | |
脾酪氨酸激酶(Syk)可参与与 MLL 重组白血病相关的信号通路。 | ||||||
Flavopiridol | 146426-40-6 | sc-202157 sc-202157A | 5 mg 25 mg | ¥880.00 ¥2866.00 | 41 | |
以 CDK9 为靶标可破坏转录延伸,而转录延伸是由 MLLT 融合蛋白控制的基因表达的关键过程。 |