[Adiponectin Receptor Agonist AdipoRon Inhibits the Proliferation of Myeloma Cells via the AMPK/Autophagy Pathway]

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020 Feb;28(1):171-176. doi: 10.19746/j.cnki.issn.1009-2137.2020.01.029.
[Article in Chinese]

Abstract

Objective: To investigate the inhibitory effect of adiponectin receptor agonist AdipoRon on proliferation of myeloma cell lines and its possible mechanism.

Methods: The myeloma cell lines Sp2/0-Ag14 and MPC-11 were treated with different concentration of AdipoRon. The cell proliferation was detected by CCK-8. Western blot was used to determine the protein level of the signaling pathway. RT-PCR was used to quantify the mRNA copy number of adiponectin receptor AdipoR1 and AdipoR2 in the bone marrow cells from 21 patients with multiple myeloma (MM). Twenty-three normal bone marrow samples were served as control.

Results: AdipoRon significantly inhibited the proliferation of MM cell lines Sp2/0-Ag14 and MPC-11 in a concentration-dependent and time-dependent manner. Western blot showed that AdipoRon induced an increase of the expression levels of apoptosis-related proteins cleaved caspase-3 and cleaved PARP. AdipoRon upregulated p-AMPK and its downstream p-ACC in MPC-11. In addition, AdipoRon upregulated LC3-II/LC3-I level and down-regulated the protein level of p62. The expression level of AdipoR1 in MM cells was significantly higher than that in normal controls, and the expression level of AdipoR2 in MM cells was significantly lower than that in normal controls.

Conclusion: Adiponectin receptors are expressed differentially between MM patients and normal subjects. AdipoRon, an adiponectin receptor agonist, can inhibit myeloma cell proliferation and induce apoptosis, and AMPK/autophagy pathway may be one of its mechanisms.

题目: 脂联素受体激动剂AdipoRon通过AMPK/自噬途径抗骨髓瘤细胞增殖.

目的: 探讨脂联素受体激动剂AdipoRon对骨髓瘤细胞系的增殖抑制作用及其可能的机制.

方法: 将不同浓度AdipoRon作用于骨髓瘤细胞系Sp2/0-Ag14和MPC-11,采用CCK-8法检测细胞增殖,Western blot检测信号通路蛋白表达水平,采用RT-PCR方法检测脂联素受体AdipoR1和AdipoR2在23例正常对照和21例多发性骨髓瘤(MM)患者骨髓单个核细胞中的表达情况.

结果: AdipoRon能显著抑制小鼠骨髓瘤细胞系Sp2/0-Ag14和MPC-11的增殖,且呈浓度依赖性和时间依赖性(r=-0.951/-0.950,r=-0.993/-0.969);AdipoRon可诱导凋亡相关蛋白cleaved caspase-3和cleaved PARP的表达水平升高;AdipoRon可上调MPC-11的p-AMPK及其下游的p-ACC磷酸化水平,且可上调LC3-II/LC3-I的水平,下调p62的蛋白水平。脂联素受体AdipoR1在MM细胞中的表达水平显著高于正常对照,而AdipoR2在MM细胞中的表达水平显著低于正常对照.

结论: 脂联素受体在MM患者和正常人之间存在差异性表达。脂联素受体激动剂AdipoRon能够抑制骨髓瘤细胞增殖及诱导细胞凋亡,AMPK/自噬途径可能是其作用机制之一.

MeSH terms

  • AMP-Activated Protein Kinases
  • Apoptosis
  • Autophagy*
  • Cell Proliferation
  • Humans
  • Multiple Myeloma*
  • Piperidines
  • Receptors, Adiponectin
  • Signal Transduction

Substances

  • AdipoRon
  • Piperidines
  • Receptors, Adiponectin
  • AMP-Activated Protein Kinases