Innovative strategies for mitochondrial dysfunction in myeloproliferative neoplasms a step toward precision medicine.

IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL
Annals of Medicine and Surgery Pub Date : 2025-08-19 eCollection Date: 2025-09-01 DOI:10.1097/MS9.0000000000003365
Shinto Bosco, Shreya Singh Beniwal, Samid Soeb Munshi, Daniela Castro Calderón, Yujin Jeong, Alyanna Cabe Cacas, Sandeep Kumar, Pedro Henrique Serra Carvalho Dos Santos, Saif Syed, Ayush Dwivedi, Mahmoud Einieh
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引用次数: 0

Abstract

Myeloproliferative neoplasms (MPNs) are clonal disorders of hematopoietic stem cells characterized by aberrant proliferation of myeloid lineages, driven primarily by mutations in JAK2, CALR, and myeloproliferative leukemia, leading to constitutive activation of the JAK-STAT pathway. Emerging evidence highlights mitochondrial dysfunction as a key factor in MPN pathogenesis, contributing to increased reactive oxygen species production, mitochondrial DNA mutations, and dysregulated mitochondrial dynamics, which collectively promote clonal expansion and apoptosis resistance. Targeting mitochondrial pathways has gained attention as a therapeutic strategy, with approaches including mitochondria-targeted antioxidants, metabolic inhibitors, and modulation of mitophagy and mitochondrial fission/fusion dynamics. However, challenges such as drug delivery specificity, therapeutic resistance, and off-target effects remain significant. Recent advances in precision medicine, incorporating genomic, transcriptomic, and proteomic profiling, offer a more personalized approach to MPN treatment by tailoring interventions to individual mutation patterns. Additionally, novel therapeutic strategies, including gene editing technologies, RNA-based therapies, and nanoparticle-mediated drug delivery systems, hold promise for overcoming current treatment limitations. The integration of artificial intelligence in drug discovery and biomarker identification further enhances the potential for targeted therapies. Future research should focus on refining these strategies, developing reliable biomarkers for patient stratification, and exploring combination therapies that enhance treatment efficacy while minimizing adverse effects. By addressing mitochondrial dysfunction as an underlying driver of MPNs, these emerging approaches have the potential to improve disease management, extend patient survival, and enhance quality of life. Also, this new approach of precision medicine allows patient stratification and ensures that treatments are formed according to the individual disease biology of each patient, which results in overall better outcomes.

Abstract Image

髓增生性肿瘤线粒体功能障碍的创新策略是迈向精准医学的一步。
骨髓增殖性肿瘤(mpn)是一种以骨髓谱系异常增殖为特征的造血干细胞克隆性疾病,主要由JAK2、CALR和骨髓增殖性白血病的突变驱动,导致JAK-STAT通路的组成性激活。新出现的证据表明,线粒体功能障碍是MPN发病的关键因素,有助于活性氧产生增加、线粒体DNA突变和线粒体动力学失调,这些因素共同促进克隆扩增和细胞凋亡抵抗。靶向线粒体途径作为一种治疗策略已经引起了人们的关注,包括靶向线粒体抗氧化剂、代谢抑制剂、线粒体自噬和线粒体裂变/融合动力学的调节。然而,诸如药物递送特异性、治疗耐药性和脱靶效应等挑战仍然显著。精确医学的最新进展,结合基因组学、转录组学和蛋白质组学分析,通过针对个体突变模式定制干预措施,为MPN治疗提供了更加个性化的方法。此外,新的治疗策略,包括基因编辑技术、基于rna的治疗和纳米颗粒介导的药物传递系统,有望克服当前的治疗局限性。人工智能在药物发现和生物标志物鉴定中的整合进一步增强了靶向治疗的潜力。未来的研究应侧重于完善这些策略,开发可靠的患者分层生物标志物,并探索提高治疗效果同时最小化不良反应的联合疗法。通过将线粒体功能障碍作为mpn的潜在驱动因素,这些新兴方法有可能改善疾病管理,延长患者生存期,提高生活质量。此外,这种精准医疗的新方法允许患者分层,并确保根据每个患者的个体疾病生物学形成治疗方法,从而获得更好的整体效果。
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
Annals of Medicine and Surgery
Annals of Medicine and Surgery MEDICINE, GENERAL & INTERNAL-
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5.90%
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