4.7 Article

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

Journal

EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 749, Issue -, Pages 107-114

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejphar.2015.01.009

Keywords

All-trans retinoic acid; C-phycocyanin; A-549 cancer cells; Apoptosis; Cell proliferation

Funding

  1. National Natural Science Foundation of China [81471546, 81001346]
  2. Medical Health Science and Technology Development Plan Project of Shandong Province [2011HZ023]
  3. Science and Technology Development Plan of Qingdao City [2012-1-3-5-(4)-nsh]
  4. Science and Technology Development Projects of Shandong province [2012YD18035]

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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.

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