Bansal Manvi, Verma Malkhey
School of Biotechnology, Banaras Hindu University, Varanasi, U.P., 221005, India.
Med Oncol. 2025 Jul 17;42(8):344. doi: 10.1007/s12032-025-02895-y.
Chronic myeloid leukemia (CML) is driven by the BCR::ABL fusion oncoprotein, caused by a reciprocal translocation between chromosomes no. 9 and 22, leading to the formation of the Philadelphia chromosome having aberrant tyrosine kinase activity. Tyrosine kinase inhibitors (TKIs) revolutionized the CML treatment and helped patients to achieve a higher survival rate. However, TKI resistance, leukemia stem cell (LSC) persistence, and disease relapse highlight the necessity for alternative treatment strategies. Furthermore, oxidative stress pathways are critical in promoting leukemic development and resistance, offering an emerging avenue for targeted intervention. This review explores several promising therapeutic targets in CML, such as suppressor pathways, autophagy modulation, the BCL-2 family proteins, and microRNAs (miRNAs) modulation. Restoring the function of tumor suppressors, such as PTPRG and p53, may complement current therapies since they are essential in regulating cell proliferation and apoptosis. Tumor suppressors offer the potential to enhance apoptosis, while the precise modulation of autophagy, a complex cellular process with context-dependent roles, can regulate cell survival under therapeutic pressure. The BCL-2 family proteins regulate apoptosis by the mitochondrial intrinsic apoptosis pathway, representing a critical target for overcoming apoptotic resistance in CML cells. Meanwhile, miRNAs emerge as potent modulators of oncogenic and apoptotic pathways by acting as tumor suppressors or oncomiRs, presenting an opportunity for advanced treatment. This review also includes gene editing to target oncogenic drivers or correcting mutations and USP inhibition to overcome resistance. Finally, it concludes by emphasizing the importance of combining these diverse therapeutic approaches with ongoing next-generation TKIs and comprehensive and personalized approaches for CML treatment, offering a path toward deeper remissions and ultimately achieving curative outcomes for CML patients.
慢性髓性白血病(CML)由BCR::ABL融合癌蛋白驱动,该蛋白由9号和22号染色体之间的相互易位引起,导致具有异常酪氨酸激酶活性的费城染色体形成。酪氨酸激酶抑制剂(TKIs)彻底改变了CML的治疗方式,帮助患者获得了更高的生存率。然而,TKI耐药、白血病干细胞(LSC)持续存在和疾病复发凸显了采用替代治疗策略的必要性。此外,氧化应激途径在促进白血病发展和耐药方面至关重要,为靶向干预提供了一条新途径。本综述探讨了CML中几个有前景的治疗靶点,如抑制途径、自噬调节、BCL-2家族蛋白和微小RNA(miRNAs)调节。恢复肿瘤抑制因子如PTPRG和p53的功能可能会补充当前的治疗方法,因为它们在调节细胞增殖和凋亡中至关重要。肿瘤抑制因子具有增强凋亡的潜力,而对自噬(一个具有依赖于上下文的作用的复杂细胞过程)的精确调节可以在治疗压力下调节细胞存活。BCL-2家族蛋白通过线粒体内在凋亡途径调节凋亡,是克服CML细胞凋亡抗性的关键靶点。同时,miRNAs通过作为肿瘤抑制因子或致癌miRNAs成为致癌和凋亡途径的有效调节因子,为先进治疗提供了机会。本综述还包括靶向致癌驱动因子或纠正突变的基因编辑以及克服耐药性的USP抑制。最后,它强调了将这些不同的治疗方法与正在进行的下一代TKIs以及CML治疗的全面和个性化方法相结合的重要性,为实现CML患者更深的缓解并最终实现治愈结果提供了一条途径。