The synergistic antitumor effects of all-trans retinoic acid and C-phycocyanin on the lung cancer A549 cells in vitro and in vivo

被引:69
作者
Li, Bing [1 ]
Gao, Mei-Hua [2 ]
Chu, Xian-Ming [3 ]
Teng, Lei [1 ]
Lv, Cong-Yi [1 ]
Yang, Peng [1 ]
Yin, Qi-Feng [1 ]
机构
[1] Qingdao Univ, Coll Med, Dept Biol, Qingdao 266021, Peoples R China
[2] Qingdao Univ, Coll Med, Dept Immunol, Qingdao 266021, Peoples R China
[3] Qingdao Univ, Affiliated Hosp, Coll Med, Dept Cardiol, Qingdao 266021, Peoples R China
基金
中国国家自然科学基金;
关键词
All-trans retinoic acid; C-phycocyanin; A-549 cancer cells; Apoptosis; Cell proliferation; MOLECULAR-MECHANISMS; INDUCED APOPTOSIS; MYELOID-LEUKEMIA; FAMILY; ATRA; MODULATION; RAT;
D O I
10.1016/j.ejphar.2015.01.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The anticancer effects and mechanism of all trans retinoic acid (ATRA), C-phycocyanin (C-PC) ATRA + C-PC on the growth of A549 cells were studied in in vitro and in vivo experiments. The effects of C-PC and ATRA on the growth of A549 cells were determined. The expression of CDK-4 and caspase-3, and the cellular apoptosis levels were detected. The tumor model was established by subcutaneous injection of A549 cells to the left axilla of the NU/NU mice. The weights of tumor and the spleen were tested. The viabilities of T-cells and spleen cells, TNF levels, the expression of Bcl-2 protein and Cyclin D1 gene were examined. Results showed both C-PC and ATRA could inhibit the growth of tumor cells in vivo and in vitro. ATRA I C-PC cooperatively showed a higher antitumor activity. The dosage of ATRA was reduced when it was administered with C-PC together, and the toxicity was reduced as well. ATRA I C-PC could decrease CDK-4 but increase caspase-3 protein expression level and induce cell apopLosis. ATRA alone could lower the activities of T lymphocytes and spleen weights, but the combination with C-PC could effectively promote viability of T cells and spleen. C-PC I ATRA could up regulate TNF, and down regulate Bcl-2 and Cyclin D1 gene. The combination might inhibit tumor growth by inhibiting the progress of cell cycle, inducing cell apopLosis and enhancing the body immunity. (C) 2015 Elsevier B.V All rights reserved.
引用
收藏
页码:107 / 114
页数:8
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