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[Blimp1、ATF4和CHOP在多发性骨髓瘤细胞中的表达及阿司匹林对其表达的影响]

[Expression of Blimp1、ATF4 and CHOP in Multiple Myeloma Cells and Effect of Aspirin on Their Expression].

作者信息

Liu Hong-Chun, Xiong Chao, Geng Jie, Liu Jun-Wen, Ren Zhen-Zhen, Li Jin, Pei Lu

机构信息

Department of Clinical Laboratorial of Examination, The First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, Henan Province, China,E-mail:

Department of Clinical Laboratorial Examination, Henan University of Traditional Chinese Medicine, ZhengZhou 450002, Henan Province, China.

出版信息

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020 Feb;28(1):165-170. doi: 10.19746/j.cnki.issn.1009-2137.2020.01.028.

Abstract

OBJECTIVE

To explore the expression of Blimp1, ATF4 and CHOP in bone marrow mononuclear cells from patients with multiple myeloma as well as the effect of aspirin on their expression.

METHODS

Sixty untreated patients with multiple myeloma and 30 patients with relatively normal bone marrow were selected. Mononuclear cells from the bone marrow fluid were separated using Ficoll separation solution. CD138 plasma cells were sorted by immunomagnetic beads method. RT-PCR was used to detect the expression levels of Blimp1, ATF4 and CHOP mRNA in U266 cells cultured in vitro. The cells were divided into blank control group, negative control group (no-loaded virus transfection) and positive experimental group [LV-Blimp1-RNAi (40051-2) transfection] by lentivirus transfection. RT-PCR was used to detect the expression of Blimp1, ATF4 and CHOP mRNA in cells of different groups. U266 cells were stimulated in vitro with different concentrations of aspirin solution (0, 0.5 mmol/L, 2.5 mmol/L, 5.0 mmol/L) for 24, 48 h and 72 h, respectively. The ability of cell proliferation in different groups was measured by CCK-8. U266 cells were stimulated with different concentrations of aspirin for 48 hours. And the mRNA expression of Blimp1, ATF4 and CHOP was detected by RT-PCR.

RESULTS

Compared with plasma cells in normal group, the expression of Blimp1 mRNA in CD138 plasma cells of MM patients significantly increased (8.040±1.878), and the mRNA expression levels of ATF4 and CHOP significantly decreased (0.735±0.089; 0.837±0.062) (P<0.05). U266 cells were cultured in vitro. Compared with the blank control group and the negative control group, the mRNA expression level of Blimp in the positive experimental group was significantly down-regulated after infection with LV-Blimp1-RNAi (40051-2) lentiviral expression vector (0.637±0.021). ATF4 and CHOP mRNA expression levels were significantly increased (1.452 ± 0.027; 1.721 ± 0.038) (P<0.05). The proliferation of U266 cells decreased after stimulation with aspirin. In the range of (0.5-5) mmol/L, aspirin could significantly inhibit the proliferation of U266 cells. The inhibition effect of aspirin was increased along with prolongation of time and increase of concentrations. After aspirin stimulation of different concentrations for 48 hours, the expression level of Blimp1 in U266 cells decreased with increasing of drug concentration, while the expression levels of ATF4 and CHOP increased with increasing of drug concentration.

CONCLUSION

Inhibition of Blimp1 expression in multiple myeloma cells can promote the expression of ATF4 and CHOP. Aspirin can inhibit the proliferation activity of myeloma cells by down-regulating Blimp1 expression in myeloma cells and up-regulating ATF4 and CHOP expression, therefore plays an anti-tumor rote.

摘要

目的

探讨Blimp1、ATF4及CHOP在多发性骨髓瘤患者骨髓单个核细胞中的表达情况以及阿司匹林对其表达的影响。

方法

选取60例初治多发性骨髓瘤患者及30例骨髓相对正常患者。采用Ficoll分离液分离骨髓液中的单个核细胞。通过免疫磁珠法分选CD138浆细胞。采用RT-PCR检测体外培养的U266细胞中Blimp1、ATF4及CHOP mRNA的表达水平。通过慢病毒转染将细胞分为空白对照组、阴性对照组(未加载病毒转染)和阳性实验组[LV-Blimp1-RNAi(40051-2)转染]。采用RT-PCR检测不同组细胞中Blimp1、ATF4及CHOP mRNA的表达。分别用不同浓度阿司匹林溶液(0、0.5 mmol/L、2.5 mmol/L、5.0 mmol/L)体外刺激U266细胞24、48 h及72 h。采用CCK-8法检测不同组细胞增殖能力。用不同浓度阿司匹林刺激U266细胞48小时。采用RT-PCR检测Blimp1、ATF4及CHOP的mRNA表达。

结果

与正常组浆细胞相比,MM患者CD138浆细胞中Blimp1 mRNA表达显著升高(8.040±1.878),ATF4及CHOP mRNA表达水平显著降低(0.735±0.089;0.837±0.062)(P<0.05)。体外培养U266细胞。与空白对照组和阴性对照组相比,感染LV-Blimp1-RNAi(40051-2)慢病毒表达载体后,阳性实验组中Blimp的mRNA表达水平显著下调(0.637±0.021)。ATF4及CHOP mRNA表达水平显著升高(1.452±0.027;1.721±0.038)(P<0.05)。阿司匹林刺激后U266细胞增殖降低。在(0.5 - 5)mmol/L范围内,阿司匹林可显著抑制U266细胞增殖。阿司匹林的抑制作用随时间延长和浓度增加而增强。不同浓度阿司匹林刺激48小时后,U266细胞中Blimp1表达水平随药物浓度增加而降低,而ATF4及CHOP表达水平随药物浓度增加而升高。

结论

抑制多发性骨髓瘤细胞中Blimp1表达可促进ATF4及CHOP表达。阿司匹林可通过下调骨髓瘤细胞中Blimp1表达、上调ATF4及CHOP表达抑制骨髓瘤细胞增殖活性,从而发挥抗肿瘤作用。

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