Total Saponins of Rubus Parvifolius L. Exhibited Anti-Leukemia Effect in vivo through STAT3 and eIF4E Signaling Pathways

被引:5
|
作者
Xu Xiao-feng [1 ]
Cheng Ru-bin [2 ]
Zhang Xue-jin [1 ]
Gao Rui-lan [3 ]
机构
[1] Hangzhou Red Cross Hosp, Dept Hematol, Hangzhou 310003, Zhejiang, Peoples R China
[2] Zhejiang Chinese Med Univ, Coll Pharmaceut Sci, Hangzhou 310053, Zhejiang, Peoples R China
[3] Zhejiang Chinese Med Univ, Affiliated Hosp 1, Hangzhou 310006, Zhejiang, Peoples R China
关键词
total saponins of Rubus parvifolius L; xenograft model; apoptosis; signal transducer and activator of transcription 3; eukaryotic initiation factor 4E; HUMAN LEUKEMIA-CELLS; APOPTOSIS; ACTIVATION; EXPRESSION; BCL-2;
D O I
10.1007/s11655-018-2563-8
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Objective: To investigate the anti-leukemia effect of total saponins of Rubus parvifolius L. (TSRP) on K562 cell xenografts in nude mice and the mechanisms of action. Methods: The K562 cell xenografts in nude mice were established, and then randomly divided into 5 groups, the control group, the cytosine arabinoside group(Ara-c) and 3 TSRP groups (20, 40 and 100 mg/kg). The tumor volume and mass of each group of nude mice were measured and the anti-tumor rates of TSRP were calculated subsequently. The apoptosis status of tumor cells was detected by hematoxylin-eosin (HE) and terminal dexynucleotidyl transferase (TdT)-mediated dUTP nick end labeling (TUNEL) staining analysis. Finally, the activities of apoptosis related signaling of signal transducer and activator of transcription 3 (STAT3), eukaryotic initiation factor 4E (eIF4E) and B-cell lymphoma-2 (bcl-2) were determined with immunohistochemistry tests. Results: Subcutaneous injection of K562 cells induced tumor formation in nude mice, and the TSRP treated group showed a significant inhibitory effect on tumor formation. The nude mice treated with TSRP showed a significant decrease in tumor growth rate and tumor weight in comparison to the control group (all P<0.05). The HE staining and TUNEL assay showed that TSRP induced cell death by apoptosis. The immunohistochemical assay showed down-regulation of the bcl-2 gene in the TSRP treated cells. The phosphorylation levels of eIF4E and STAT3 were decreased obviously after the treatment of TSRP. Conclusion: TSRP had an excellent tumor-suppressing effect on K562 cells in the nude mice xenograft model, suggesting that TSPR can be developed as a promising anti-chronic myeloide leukemia drug.
引用
收藏
页码:920 / 924
页数:5
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