Research progress in Menin-MLL interaction and its inhibitors in MLL-rearranged leukemia

Acute leukemias caused by mixed lineage leukemia (MLL) gene rearrangements (MLL-r) are characterized by high invasiveness and a poor prognosis, with few specific treatment options available. MLL protein is essential in embryonic development and hematopoiesis. It exhibits histone methyltransferase ac...

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Main Authors: FANG Xinyue, SHI Lan, XIA Siyi, WANG Jiaxuan, WU Yingli, HE Kejun
Format: Article
Language:zho
Published: Editorial Office of Journal of Shanghai Jiao Tong University (Medical Science) 2024-10-01
Series:Shanghai Jiaotong Daxue xuebao. Yixue ban
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Online Access:https://xuebao.shsmu.edu.cn/CN/10.3969/j.issn.1674-8115.2024.10.011
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author FANG Xinyue
SHI Lan
XIA Siyi
WANG Jiaxuan
WU Yingli
HE Kejun
author_facet FANG Xinyue
SHI Lan
XIA Siyi
WANG Jiaxuan
WU Yingli
HE Kejun
author_sort FANG Xinyue
collection DOAJ
description Acute leukemias caused by mixed lineage leukemia (MLL) gene rearrangements (MLL-r) are characterized by high invasiveness and a poor prognosis, with few specific treatment options available. MLL protein is essential in embryonic development and hematopoiesis. It exhibits histone methyltransferase activity and can interact with various proteins through its functional domains, thus regulating downstream target gene expression through epigenetic modifications. MLL-r leads to the formation of MLL fusion proteins (MLL-FPs), in which the C-terminal is replaced by fusion partner proteins; over 100 such partner proteins have been identified to date. In numerous studies of the molecular mechanism, Menin serves as an important cofacter in the leukemogenesis of MLL-FPs and participates in forming the key complex when interacting with the N terminal of MLL protein, resulting in the disregulation of certain targeted genes, which makes the development of Menin-MLL inhibitors theoretically possible. To date, several small molecules have been identified that inhibit Menin-MLL interaction, including thienopyrimidine derivatives, piperidine derivatives, pyrimidine derivatives, and macrocyclic mimic peptides. Based on these prototypes, at least seven drugs are currently undergoing clinical evaluation, with some promising preliminary data regarding safety, tolerability, and efficacy. This review summarizes the structure and function of MLL, the mechanism of the occurrence of MLL-r leukemia, and current Menin-MLL inhibitors tested in MLL-r leukemia.
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spelling doaj-art-f9d854c8ca9b48b2a80ea198221bb7112024-11-13T03:13:33ZzhoEditorial Office of Journal of Shanghai Jiao Tong University (Medical Science)Shanghai Jiaotong Daxue xuebao. Yixue ban1674-81152024-10-0144101287129810.3969/j.issn.1674-8115.2024.10.0111674-8115(2024)10-1287-12Research progress in Menin-MLL interaction and its inhibitors in MLL-rearranged leukemiaFANG Xinyue0SHI Lan1XIA Siyi2WANG Jiaxuan3WU Yingli4HE Kejun5Faculty of Clinical Medicine, Shanghai Jiao Tong University School of Medicine, Shanghai200025, ChinaFaculty of Clinical Medicine, Shanghai Jiao Tong University School of Medicine, Shanghai200025, ChinaFaculty of Clinical Medicine, Shanghai Jiao Tong University School of Medicine, Shanghai200025, ChinaFaculty of Clinical Medicine, Shanghai Jiao Tong University School of Medicine, Shanghai200025, ChinaDepartment of Pathophysiology, Shanghai Jiao Tong University College of Basic Medical Sciences, Shanghai200025, ChinaPediatric Hematology and Oncology, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai200092, ChinaAcute leukemias caused by mixed lineage leukemia (MLL) gene rearrangements (MLL-r) are characterized by high invasiveness and a poor prognosis, with few specific treatment options available. MLL protein is essential in embryonic development and hematopoiesis. It exhibits histone methyltransferase activity and can interact with various proteins through its functional domains, thus regulating downstream target gene expression through epigenetic modifications. MLL-r leads to the formation of MLL fusion proteins (MLL-FPs), in which the C-terminal is replaced by fusion partner proteins; over 100 such partner proteins have been identified to date. In numerous studies of the molecular mechanism, Menin serves as an important cofacter in the leukemogenesis of MLL-FPs and participates in forming the key complex when interacting with the N terminal of MLL protein, resulting in the disregulation of certain targeted genes, which makes the development of Menin-MLL inhibitors theoretically possible. To date, several small molecules have been identified that inhibit Menin-MLL interaction, including thienopyrimidine derivatives, piperidine derivatives, pyrimidine derivatives, and macrocyclic mimic peptides. Based on these prototypes, at least seven drugs are currently undergoing clinical evaluation, with some promising preliminary data regarding safety, tolerability, and efficacy. This review summarizes the structure and function of MLL, the mechanism of the occurrence of MLL-r leukemia, and current Menin-MLL inhibitors tested in MLL-r leukemia.https://xuebao.shsmu.edu.cn/CN/10.3969/j.issn.1674-8115.2024.10.011mll-rearranged leukemiamenintargeted therapymenin-mll inhibitor
spellingShingle FANG Xinyue
SHI Lan
XIA Siyi
WANG Jiaxuan
WU Yingli
HE Kejun
Research progress in Menin-MLL interaction and its inhibitors in MLL-rearranged leukemia
Shanghai Jiaotong Daxue xuebao. Yixue ban
mll-rearranged leukemia
menin
targeted therapy
menin-mll inhibitor
title Research progress in Menin-MLL interaction and its inhibitors in MLL-rearranged leukemia
title_full Research progress in Menin-MLL interaction and its inhibitors in MLL-rearranged leukemia
title_fullStr Research progress in Menin-MLL interaction and its inhibitors in MLL-rearranged leukemia
title_full_unstemmed Research progress in Menin-MLL interaction and its inhibitors in MLL-rearranged leukemia
title_short Research progress in Menin-MLL interaction and its inhibitors in MLL-rearranged leukemia
title_sort research progress in menin mll interaction and its inhibitors in mll rearranged leukemia
topic mll-rearranged leukemia
menin
targeted therapy
menin-mll inhibitor
url https://xuebao.shsmu.edu.cn/CN/10.3969/j.issn.1674-8115.2024.10.011
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