Role of SIRT1 in Chemoresistant Leukemia
-
Published:2023-09-23
Issue:19
Volume:24
Page:14470
-
ISSN:1422-0067
-
Container-title:International Journal of Molecular Sciences
-
language:en
-
Short-container-title:IJMS
Author:
Fajardo-Orduña Guadalupe Rosario1ORCID, Ledesma-Martínez Edgar1ORCID, Aguiñiga-Sanchez Itzen12ORCID, Weiss-Steider Benny1, Santiago-Osorio Edelmiro1ORCID
Affiliation:
1. Hematopoiesis and Leukemia Laboratory, Research Unit on Cell Differentiation and Cancer, Faculty of High Studies Zaragoza, National Autonomous University of Mexico, Mexico City 09230, Mexico 2. Department of Biomedical Sciences, School of Medicine, Faculty of High Studies Zaragoza, National Autonomous University of Mexico, Mexico City 56410, Mexico
Abstract
Leukemias of the AML, CML, and CLL types are the most common blood cancers worldwide, making them a major global public health problem. Furthermore, less than 24% of patients treated with conventional chemotherapy (low-risk patients) and 10–15% of patients ineligible for conventional chemotherapy (high-risk patients) survive five years. The low levels of survival are mainly due to toxicity and resistance to chemotherapy or other medication, the latter leading to relapse of the disease, which is the main obstacle to the treatment of leukemia. Drug resistance may include different molecular mechanisms, among which epigenetic regulators are involved. Silent information regulator 2 homolog 1 (SIRT1) is an epigenetic factor belonging to the sirtuin (SIRT) family known to regulate aspects of chromatin biology, genome stability, and metabolism, both in homeostasis processes and in different diseases, including cancer. The regulatory functions of SIRT1 in different biological processes and molecular pathways are dependent on the type and stage of the neoplasia; thus, it may act as both an oncogenic and tumor suppressor factor and may also participate in drug resistance. In this review, we explore the role of SIRT1 in drug-resistant leukemia and its potential as a therapeutic target.
Funder
General Directorate of Academic Personnel Affairs, National Autonomous University of Mexico
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis
Reference93 articles.
1. SIRT1 prevents genotoxic stress-induced p53 activation in acute myeloid leukemia;Sasca;Blood,2014 2. Tang, Y.-L., Zhang, C.G., Liu, H., Zhou, Y., Wang, Y.P., Li, Y., and Wang, C.L. (2020). Ginsenoside Rg1 Inhibits Cell Proliferation and Induces Markers of Cell Senescence in CD34+CD38− Leukemia Stem Cells Derived from KG1α Acute Myeloid Leukemia Cells by Activating the Sirtuin 1 (SIRT1)/Tuberous Sclerosis Complex 2 (TSC2) Signaling Pathway. Med. Sci. Monit. Int. Med. J. Exp. Clin. Res., 26. 3. A Therapeutically Targetable NOTCH1-SIRT1-KAT7 Axis in T-cell Leukemia;Lancho;Blood Cancer Discov.,2023 4. Wang, Z., Zhang, C., Warden, C.D., Liu, Z., Yuan, Y.-C., Guo, C., Wang, C., Wang, J., Wu, X., and Ermel, R. (2022). Loss of SIRT1 inhibits hematopoietic stem cell aging and age-dependent mixed phenotype acute leukemia. Commun. Biol., 5. 5. Role of SIRT1 in the growth and regulation of normal hematopoietic and leukemia stem cells;Li;Curr. Opin. Hematol.,2015
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|