黏附分子在多发性骨髓瘤肿瘤发生和靶向治疗中的作用

M. Bou Zerdan, L. Nasr, J. Kassab, Ludovic Saba, Myriam Ghossein, M. Yaghi, B. Dominguez, C. Chaulagain
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引用次数: 9

摘要

每一天,我们都离找到多发性骨髓瘤的治疗方法更近了一步。骨髓瘤细胞通过特化的细胞网络和细胞因子系统造成损伤。在这些相互作用中隐含着细胞粘附分子及其调节因子,包括但不限于整合素和syndecan-1/CD138,免疫球蛋白超家族细胞粘附分子,如CD44,钙粘蛋白,如n-钙粘蛋白,和选择蛋白,如e -选择素。几种粘附分子分别参与了骨髓瘤的形成过程,如从意义不明的前体疾病单克隆γ病到惰性无症状多发性骨髓瘤(阴性骨髓瘤)再到活动性多发性骨髓瘤或原发性浆细胞白血病的转变,以及多发性骨髓瘤的病理表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adhesion molecules in multiple myeloma oncogenesis and targeted therapy
Every day we march closer to finding the cure for multiple myeloma. The myeloma cells inflict their damage through specialized cellular meshwork and cytokines system. Implicit in these interactions are cellular adhesion molecules and their regulators which include but are not limited to integrins and syndecan-1/CD138, immunoglobulin superfamily cell adhesion molecules, such as CD44, cadherins such as N-cadherin, and selectins, such as E-selectin. Several adhesion molecules are respectively involved in myelomagenesis such as in the transition from the precursor disorder monoclonal gammopathy of undetermined significance to indolent asymptomatic multiple myeloma (smoldering myeloma) then to active multiple myeloma or primary plasma cell leukemia, and in the pathological manifestations of multiple myeloma.
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来源期刊
自引率
0.00%
发文量
3
审稿时长
13 weeks
期刊介绍: International Journal of Hematologic Oncology welcomes unsolicited article proposals. Email us today to discuss the suitability of your research and our options for authors, including Accelerated Publication. Find out more about publishing open access with us here.
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