Ghadyani Nejhad Laya, Sohani Mahsa, Ghandforoush Nasrin Alizad, Nikbakht Mohsen, Mohammadi Saeed, Vaezi Mohammad, Rostami Shahrbano, Chahardouli Bahram
Hematologic Malignancies Research Center, Research Institute for Oncology, Hematology and Cell Therapy, Tehran University of Medical Sciences, Iran.
Student Research Committee, Department of Hematology and Blood Banking, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Leuk Res Rep. 2025 May 9;23:100513. doi: 10.1016/j.lrr.2025.100513. eCollection 2025.
Chronic myeloid leukemia (CML), is a myeloproliferative disease characterized by unregulated growth of blood forming cells in bone marrow and blood. The t(9;22)(q34;q11.2) translocation, which results in the formation of a hyperactive tyrosine kinase (), is a hallmark of this disorder. Tyrosine kinase inhibitors such as imatinib has shown a great promise in reduction of CML cells. However, development of resistance to tyrosine kinase inhibitors has raised a great clinical concern about their future applications. Recently, non-coding RNAs, have shown to play significant regulatory roles in development of chemoresistance in CML cells. Discovering the underlying mechanisms of these non-coding RNAs might provide new opportunities for treating chemo-resistant forms of CML. These non-coding RNAs could be considered valuable therapeutic targets if they are found to play a role in the development of chemoresistance in CML cells. We mentioned the identified non-coding RNAs in development of chemoresistance in CML cells.
慢性髓性白血病(CML)是一种骨髓增殖性疾病,其特征是骨髓和血液中造血细胞的生长不受调控。t(9;22)(q34;q11.2)易位导致形成一种活性过高的酪氨酸激酶,这是该疾病的一个标志。酪氨酸激酶抑制剂如伊马替尼在减少CML细胞方面显示出巨大前景。然而,对酪氨酸激酶抑制剂产生耐药性的问题引发了人们对其未来应用的重大临床担忧。最近,非编码RNA已被证明在CML细胞化疗耐药性的发展中发挥重要调节作用。发现这些非编码RNA的潜在机制可能为治疗化疗耐药型CML提供新机会。如果发现这些非编码RNA在CML细胞化疗耐药性的发展中起作用,它们可被视为有价值的治疗靶点。我们提到了在CML细胞化疗耐药性发展中已鉴定出的非编码RNA。