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氯化锂通过激活Wnt/β-连环蛋白通路抑制多发性骨髓瘤细胞的存活、克服耐药性并引发细胞凋亡。

Lithium chloride inhibits cell survival, overcomes drug resistance, and triggers apoptosis in multiple myeloma via activation of the Wnt/β-catenin pathway.

作者信息

Yao Ruosi, Sun Xiaoyang, Xie Yu, Liu Linlin, Han Danyang, Yao Yao, Li Hujun, Li Zhenyu, Xu Kailin

机构信息

Blood Diseases Institute, Xuzhou Medical University Xuzhou, Jiangsu, China.

Department of Hematology, The Affiliated Hospital of Xuzhou Medical University Xuzhou, Jiangsu, China.

出版信息

Am J Transl Res. 2018 Aug 15;10(8):2610-2618. eCollection 2018.

Abstract

Multiple myeloma (MM) is an extremely malignant plasma cell disease, which is still incurable due to its drug resistance. Lithium chloride (LiCl) functions in many pathological processes, including bipolar disorder, acute brain injuries, and chronic neurodegenerative diseases, but its antagonistic role in MM progression has not been reported thus far. In this study, we found that LiCl inhibited MM cell proliferation and induced MM cell cycle G2/M phase arrest in a dose-dependent manner. Moreover, LiCl overcomes bortezomib (BTZ)-mediated resistance in MM cells and induces apoptosis in BTZ-resistant cells. Our data preliminarily indicate that LiCl induces MM cell apoptosis via activating the Wnt/β-catenin signaling pathway. Overall, our results define LiCl as an inducer of MM cell apoptosis and unveil a crosstalk between BTZ and LiCl in facilitating cell apoptosis.

摘要

多发性骨髓瘤(MM)是一种极其恶性的浆细胞疾病,由于其耐药性,目前仍然无法治愈。氯化锂(LiCl)在许多病理过程中发挥作用,包括双相情感障碍、急性脑损伤和慢性神经退行性疾病,但迄今为止,其在MM进展中的拮抗作用尚未见报道。在本研究中,我们发现LiCl以剂量依赖性方式抑制MM细胞增殖并诱导MM细胞周期G2/M期阻滞。此外,LiCl克服了硼替佐米(BTZ)介导的MM细胞耐药性,并诱导BTZ耐药细胞凋亡。我们的数据初步表明,LiCl通过激活Wnt/β-连环蛋白信号通路诱导MM细胞凋亡。总体而言,我们的结果将LiCl定义为MM细胞凋亡的诱导剂,并揭示了BTZ与LiCl在促进细胞凋亡方面的相互作用。

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