Ramakrishnan Vijay, D'Souza Anita
Division of Hematology, Mayo Clinic, 200, First Street SW, Rochester, MN, 55905, USA.
Medical College of Wisconsin Milwaukee, Milwaukee, WI, 53226, USA.
Curr Hematol Malig Rep. 2016 Apr;11(2):156-64. doi: 10.1007/s11899-016-0315-4.
Multiple myeloma (MM) is a devastating malignancy of antibody-producing plasma cells. In the absence of a single unifying genetic event contributing to disease manifestation, efforts have focused on understanding signaling events deregulated in myeloma plasma cells. MM cells are dependent on both cellular and non-cellular components of the tumor microenvironment such as bone marrow stromal cells, endothelial cells, and cytokines such as interleukin 6 (IL6), vascular endothelial growth factor (VEGF), and insulin-like growth factor (IGF) for their growth and survival. The cumulative effect of such interactions is the aberrant activation of numerous signal transduction pathways within the MM plasma cells leading to uncontrolled growth and prevention of apoptosis. Here, we will review our current understanding of some of the key signal transduction pathways dysregulated in MM and emerging therapies targeting these pathways in MM.
多发性骨髓瘤(MM)是一种由产生抗体的浆细胞引发的毁灭性恶性肿瘤。由于缺乏导致疾病表现的单一统一遗传事件,研究重点已集中在了解骨髓瘤浆细胞中失调的信号传导事件。MM细胞的生长和存活依赖于肿瘤微环境的细胞和非细胞成分,如骨髓基质细胞、内皮细胞以及白细胞介素6(IL6)、血管内皮生长因子(VEGF)和胰岛素样生长因子(IGF)等细胞因子。这种相互作用的累积效应是MM浆细胞内众多信号转导通路的异常激活,导致生长失控和细胞凋亡受阻。在此,我们将综述目前对MM中一些关键信号转导通路失调的理解以及针对这些通路的MM新兴疗法。