Update on the Progress of Musashi-2 in Malignant Tumors

Since the discovery of the Musashi (MSI) protein, its ability to affect the mitosis of Drosophila progenitor cells has garnered significant interest among scientists. In the following 20 years, it has lived up to expectations. A substantial body of evidence has demonstrated that it is closely relate...

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Main Authors: Yiting Niu, Tao Zhou, Yanjun Li
Format: Article
Language:English
Published: IMR Press 2025-01-01
Series:Frontiers in Bioscience-Landmark
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Online Access:https://www.imrpress.com/journal/FBL/30/1/10.31083/FBL24928
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author Yiting Niu
Tao Zhou
Yanjun Li
author_facet Yiting Niu
Tao Zhou
Yanjun Li
author_sort Yiting Niu
collection DOAJ
description Since the discovery of the Musashi (MSI) protein, its ability to affect the mitosis of Drosophila progenitor cells has garnered significant interest among scientists. In the following 20 years, it has lived up to expectations. A substantial body of evidence has demonstrated that it is closely related to the development, metastasis, migration, and drug resistance of malignant tumors. In recent years, research on the MSI protein has advanced, and many novel viewpoints and drug resistance attempts have been derived; for example, tumor protein p53 mutations and MSI-binding proteins lead to resistance to protein arginine N-methyltransferase 5-targeted therapy in lymphoma patients. Moreover, the high expression of MSI2 in pancreatic cancer might suppress its development and progression. As a significant member of the MSI family, MSI2 is closely associated with multiple malignant tumors, including hematological disorders, common abdominal tumors, and other tumor types (e.g., glioblastoma, breast cancer). MSI2 is highly expressed in the majority of tumors and is related to a poor disease prognosis. However, its specific expression levels and regulatory mechanisms may differ based on the tumor type. This review summarizes the research progress related to MSI2 in recent years, including its occurrence, migration mechanism, and drug resistance, as well as the prospect of developing tumor immunosuppressants and biomarkers.
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spelling doaj-art-52e52b431fc0446bb2948f4eda82cc772025-01-25T08:55:52ZengIMR PressFrontiers in Bioscience-Landmark2768-67012025-01-013012492810.31083/FBL24928S2768-6701(24)01442-4Update on the Progress of Musashi-2 in Malignant TumorsYiting Niu0Tao Zhou1Yanjun Li2Department of Hepatobiliary and Pancreatic Surgery, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, 030032 Taiyuan, Shanxi, ChinaDepartment of Hepatobiliary Surgery, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, 030032 Taiyuan, Shanxi, ChinaDepartment of Hepatobiliary and Pancreatic Surgery, Shanxi Bethune Hospital, Shanxi Academy of Medical Sciences, Tongji Shanxi Hospital, Third Hospital of Shanxi Medical University, 030032 Taiyuan, Shanxi, ChinaSince the discovery of the Musashi (MSI) protein, its ability to affect the mitosis of Drosophila progenitor cells has garnered significant interest among scientists. In the following 20 years, it has lived up to expectations. A substantial body of evidence has demonstrated that it is closely related to the development, metastasis, migration, and drug resistance of malignant tumors. In recent years, research on the MSI protein has advanced, and many novel viewpoints and drug resistance attempts have been derived; for example, tumor protein p53 mutations and MSI-binding proteins lead to resistance to protein arginine N-methyltransferase 5-targeted therapy in lymphoma patients. Moreover, the high expression of MSI2 in pancreatic cancer might suppress its development and progression. As a significant member of the MSI family, MSI2 is closely associated with multiple malignant tumors, including hematological disorders, common abdominal tumors, and other tumor types (e.g., glioblastoma, breast cancer). MSI2 is highly expressed in the majority of tumors and is related to a poor disease prognosis. However, its specific expression levels and regulatory mechanisms may differ based on the tumor type. This review summarizes the research progress related to MSI2 in recent years, including its occurrence, migration mechanism, and drug resistance, as well as the prospect of developing tumor immunosuppressants and biomarkers.https://www.imrpress.com/journal/FBL/30/1/10.31083/FBL24928musashi-2hepatocellular carcinomacancerepithelial–mesenchymal transition
spellingShingle Yiting Niu
Tao Zhou
Yanjun Li
Update on the Progress of Musashi-2 in Malignant Tumors
Frontiers in Bioscience-Landmark
musashi-2
hepatocellular carcinoma
cancer
epithelial–mesenchymal transition
title Update on the Progress of Musashi-2 in Malignant Tumors
title_full Update on the Progress of Musashi-2 in Malignant Tumors
title_fullStr Update on the Progress of Musashi-2 in Malignant Tumors
title_full_unstemmed Update on the Progress of Musashi-2 in Malignant Tumors
title_short Update on the Progress of Musashi-2 in Malignant Tumors
title_sort update on the progress of musashi 2 in malignant tumors
topic musashi-2
hepatocellular carcinoma
cancer
epithelial–mesenchymal transition
url https://www.imrpress.com/journal/FBL/30/1/10.31083/FBL24928
work_keys_str_mv AT yitingniu updateontheprogressofmusashi2inmalignanttumors
AT taozhou updateontheprogressofmusashi2inmalignanttumors
AT yanjunli updateontheprogressofmusashi2inmalignanttumors