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靶向多发性骨髓瘤中的自噬

Targeting autophagy in multiple myeloma.

作者信息

Yun Zhuang, Zhichao Jin, Hao Yao, Ou Ji, Ran Yang, Wen Dong, Qun Shen

机构信息

Hematology Department, The First Affiliated Hospital of Nanjing University of Chinese Medicine, Hanzhong Road No.155, Baixia District, Nanjing 210029, Jiangsu Province, China; Nanjing University of Traditional Chinese Medicine, Xianlin Avenue No.138, Qixia District, Nanjing 210046, Jiangsu Province, China.

Department of Oncology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, No. 5 Beixiange, Xicheng District, Beijing 100053, China.

出版信息

Leuk Res. 2017 Aug;59:97-104. doi: 10.1016/j.leukres.2017.06.002. Epub 2017 Jun 3.

Abstract

Autophagy plays an important role in plasma cell ontogeny and in the pathophysiology of multiple myeloma. Autophagy is usually considered a pro-survival mechanism, and cooperates with the ubiquitin proteasome system in maintaining the homeostasis of myeloma cells by degrading excessive and misfolded proteins for energy recycling. Therefore, the inhibition of autophagy could effectively induce death in myeloma cells, and could synergize with proteasome inhibitors. However, the excessive activation of autophagy could also lead to the extreme degradation of the organelles that induce autophagic cell death. Hence, the activation of autophagic cell death might also represent a promising approach for treating myeloma. Recent studies have demonstrated that autophagy also mediates drug resistance in myeloma cells and the complications of myeloma, while the inhibition of autophagy may reverse the response to drugs. In this study, we have mainly reviewed recent research on autophagy in relationship to the therapeutic effect, the reversal of drug resistance, and the mediation of complications.

摘要

自噬在浆细胞发生及多发性骨髓瘤的病理生理学中发挥着重要作用。自噬通常被认为是一种促生存机制,它与泛素蛋白酶体系统协同作用,通过降解过量及错误折叠的蛋白质以进行能量循环,从而维持骨髓瘤细胞的稳态。因此,抑制自噬可有效诱导骨髓瘤细胞死亡,并可与蛋白酶体抑制剂产生协同作用。然而,自噬的过度激活也可能导致细胞器的过度降解,进而诱导自噬性细胞死亡。因此,激活自噬性细胞死亡也可能是治疗骨髓瘤的一种有前景的方法。最近的研究表明,自噬还介导骨髓瘤细胞的耐药性及骨髓瘤的并发症,而抑制自噬可能会逆转对药物的反应。在本研究中,我们主要综述了近期关于自噬与治疗效果、耐药性逆转及并发症介导相关的研究。

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