Role of SIRT1 in Chemoresistant Leukemia.
Guadalupe Rosario Fajardo-OrduñaEdgar Ledesma-MartínezItzen Aguiñiga-SánchezBenny Weiss-SteiderEdelmiro Santiago-OsorioPublished in: International journal of molecular sciences (2023)
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.
Keyphrases
- end stage renal disease
- drug resistant
- public health
- newly diagnosed
- ejection fraction
- oxidative stress
- gene expression
- peritoneal dialysis
- bone marrow
- prognostic factors
- healthcare
- ischemia reperfusion injury
- multidrug resistant
- squamous cell carcinoma
- dna damage
- emergency department
- genome wide
- locally advanced
- acute lymphoblastic leukemia
- young adults
- acinetobacter baumannii
- smoking cessation
- combination therapy
- electronic health record
- allogeneic hematopoietic stem cell transplantation