TY - JOUR
T1 - Macrophages are an abundant component of myeloma microenvironment and protect myeloma cells from chemotherapy drug-induced apoptosis
AU - Zheng, Yuhuan
AU - Cai, Zhen
AU - Wang, Siqing
AU - Zhang, Xiang
AU - Qian, Jianfei
AU - Hong, Sungyoul
AU - Li, Haiyan
AU - Wang, Michael
AU - Yang, Jing
AU - Yi, Qing
N1 - Copyright:
Copyright 2021 Elsevier B.V., All rights reserved.
PY - 2009
Y1 - 2009
N2 - Multiple myeloma remains an incurable disease. One of the major problems is that myeloma cells develop drug resistance on interaction with bone marrow stromal cells. In this study, we examined the effects of macrophages (MΦs), a type of stromal cells, on myeloma cell survival and response to chemotherapy. We showed that MΦ, in particular tumorassociated MΦ, is a protector of myeloma cells. The protective effect was dependent on direct contact between MΦs and myeloma cells. MΦs protected both myeloma cell lines and primary myeloma cells from spontaneous and chemotherapy drug-induced apoptosis by attenuating the activation and cleavage of caspase-dependent apoptotic signaling. These findings are clinically relevant because we found that CD68+ MΦs heavily infiltrate the bone marrow of patients with myeloma but not the bone marrow of control patients. Thus, our results indicate that MΦs may contribute to myeloma cell survival and resistance to chemotherapeutic treatment in vivo.
AB - Multiple myeloma remains an incurable disease. One of the major problems is that myeloma cells develop drug resistance on interaction with bone marrow stromal cells. In this study, we examined the effects of macrophages (MΦs), a type of stromal cells, on myeloma cell survival and response to chemotherapy. We showed that MΦ, in particular tumorassociated MΦ, is a protector of myeloma cells. The protective effect was dependent on direct contact between MΦs and myeloma cells. MΦs protected both myeloma cell lines and primary myeloma cells from spontaneous and chemotherapy drug-induced apoptosis by attenuating the activation and cleavage of caspase-dependent apoptotic signaling. These findings are clinically relevant because we found that CD68+ MΦs heavily infiltrate the bone marrow of patients with myeloma but not the bone marrow of control patients. Thus, our results indicate that MΦs may contribute to myeloma cell survival and resistance to chemotherapeutic treatment in vivo.
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U2 - 10.1182/blood-2009-05-220285
DO - 10.1182/blood-2009-05-220285
M3 - Article
C2 - 19710503
AN - SCOPUS:70449477633
VL - 114
SP - 3625
EP - 3628
JO - Unknown Journal
JF - Unknown Journal
IS - 17
ER -