Bone marrow microenvironment in myelodysplastic neoplasms: insights into pathogenesis, biomarkers, and therapeutic targets.

IF 5.3 2区 医学 Q1 ONCOLOGY
Forouzan Bahmani, Maryam Shayanmanesh, Mahdi Safari, Amirarsalan Alaei, Yasaman Pouriafar, Zahra Rasti, Farhad Zaker, Shahrbano Rostami, Fatemeh Damerchiloo, Majid Safa
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引用次数: 0

Abstract

Myelodysplastic neoplasms (MDS) represent a heterogeneous group of malignant hematopoietic stem and progenitor cell (HSPC) disorders characterized by cytopenia, ineffective hematopoiesis, as well as the potential to progress to acute myeloid leukemia (AML). The pathogenesis of MDS is influenced by intrinsic factors, such as genetic insults, and extrinsic factors, including altered bone marrow microenvironment (BMM) composition and architecture. BMM is reprogrammed in MDS, initially to prevent the development of the disease but eventually to provide a survival advantage to dysplastic cells. Recently, inflammation or age-related inflammation in the bone marrow has been identified as a key pathogenic mechanism for MDS. Inflammatory signals trigger stress hematopoiesis, causing HSPCs to emerge from quiescence and resulting in MDS development. A better understanding of the role of the BMM in the pathogenesis of MDS has opened up new avenues for improving diagnosis, prognosis, and treatment of the disease. This article provides a comprehensive review of the current knowledge regarding the significance of the BMM to MDS pathophysiology and highlights recent advances in developing innovative therapies.

骨髓增生异常肿瘤的骨髓微环境:发病机制、生物标志物和治疗靶点的见解。
骨髓增生异常肿瘤(MDS)是一种异质性的恶性造血干细胞和祖细胞(HSPC)疾病,其特征是细胞减少、造血功能无效,以及进展为急性髓性白血病(AML)的潜力。MDS的发病机制受遗传损伤等内在因素和骨髓微环境(BMM)组成和结构改变等外在因素的影响。BMM在MDS中被重新编程,最初是为了防止疾病的发展,但最终为发育不良的细胞提供生存优势。近年来,骨髓炎症或与年龄相关的炎症已被确定为MDS的关键致病机制。炎症信号触发应激造血,导致HSPCs从静止状态出现并导致MDS的发展。更好地了解BMM在MDS发病机制中的作用,为改善该病的诊断、预后和治疗开辟了新的途径。这篇文章提供了关于BMM对MDS病理生理意义的当前知识的全面回顾,并强调了开发创新疗法的最新进展。
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
CiteScore
10.90
自引率
1.70%
发文量
360
审稿时长
1 months
期刊介绍: Cancer Cell International publishes articles on all aspects of cancer cell biology, originating largely from, but not limited to, work using cell culture techniques. The journal focuses on novel cancer studies reporting data from biological experiments performed on cells grown in vitro, in two- or three-dimensional systems, and/or in vivo (animal experiments). These types of experiments have provided crucial data in many fields, from cell proliferation and transformation, to epithelial-mesenchymal interaction, to apoptosis, and host immune response to tumors. Cancer Cell International also considers articles that focus on novel technologies or novel pathways in molecular analysis and on epidemiological studies that may affect patient care, as well as articles reporting translational cancer research studies where in vitro discoveries are bridged to the clinic. As such, the journal is interested in laboratory and animal studies reporting on novel biomarkers of tumor progression and response to therapy and on their applicability to human cancers.
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