Mechanisms and signaling pathways of tyrosine kinase inhibitor resistance in chronic myeloid leukemia: A comprehensive review.

IF 0.9 Q4 HEMATOLOGY
Leukemia Research Reports Pub Date : 2025-08-05 eCollection Date: 2025-01-01 DOI:10.1016/j.lrr.2025.100533
Meriem Lahmouad, Zahrae Rachid, Rawane Bellemrrabet, Jihane Zerrouk, Khan Wen Goh, Abdelhakim Bouyahya, Youssef Aboussalah
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引用次数: 0

Abstract

Chronic Myeloid Leukemia (CML) is characterized by aberrant BCR::ABL1 tyrosine kinase activity in hematopoietic stem cells. Although tyrosine kinase inhibitors (TKIs) have revolutionized CML treatment, resistance remains a major clinical challenge. This review provides a comprehensive overview of CML, including its epidemiology, pathophysiology, diagnosis, and treatment, as outlined in the latest WHO consensus classification. Current treatment paradigms and the prospects for treatment-free remission (TFR) are also explored. The primary focus is on elucidating the molecular mechanisms of TKI resistance, emphasizing both well-known pathways such as PI3K/AKT, MAPK, JAK/STAT, and alternative pathways including SRC/AKT. This review stands out by integrating recent discoveries regarding genetic mutations within the BCR::ABL1 gene, alongside other molecular alterations contributing to resistance. By synthesizing this knowledge, it aims to guide clinical practitioners, investigators, and translational researchers in developing innovative strategies to overcome resistance and improve patient outcomes in CML.

慢性髓性白血病中酪氨酸激酶抑制剂耐药的机制和信号通路综述。
慢性髓系白血病(CML)以造血干细胞中BCR::ABL1酪氨酸激酶活性异常为特征。虽然酪氨酸激酶抑制剂(TKIs)已经彻底改变了CML的治疗,但耐药性仍然是一个主要的临床挑战。本综述提供了CML的全面概述,包括其流行病学、病理生理学、诊断和治疗,概述了最新的世卫组织共识分类。目前的治疗模式和前景的无治疗缓解(TFR)也进行了探讨。主要重点是阐明TKI耐药的分子机制,强调PI3K/AKT、MAPK、JAK/STAT等众所周知的途径,以及包括SRC/AKT在内的替代途径。这篇综述通过整合最近关于BCR::ABL1基因突变的发现,以及其他有助于耐药的分子改变,脱颖而出。通过综合这些知识,它旨在指导临床从业者,研究者和转化研究人员开发创新策略来克服耐药性并改善CML患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Leukemia Research Reports
Leukemia Research Reports Medicine-Oncology
CiteScore
1.70
自引率
0.00%
发文量
70
审稿时长
23 weeks
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