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April 2012 Volume 5 Issue 4

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Article

Tanshinone IIA inhibits human breast cancer MDA-MB-231 cells by decreasing LC3-II, Erb-B2 and NF-κBp65

  • Authors:
    • Chin-Cheng Su
    • Su-Yu Chien
    • Shou-Jen Kuo
    • Yao-Li Chen
    • Chun-Yuan Cheng
    • Dar-Ren Chen
  • View Affiliations / Copyright

    Affiliations: Department of Surgery, Comprehensive Breast Cancer Center, Laboratory of Integrative Medicine Cancer Research, Changhua Christian Hospital, Changhua 500-06, Taiwan, R.O.C., Department of Pharmacy, Comprehensive Breast Cancer Center, Changhua Christian Hospital, Changhua 500-06, Taiwan, R.O.C., Department of Surgery, Comprehensive Breast Cancer Center, Changhua Christian Hospital, Changhua 500-06, Taiwan, R.O.C.
  • Pages: 1019-1022
    |
    Published online on: January 13, 2012
       https://doi.org/10.3892/mmr.2012.756
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Abstract

The ability of tanshinone IIA (Tan-IIA) to inhibit the proliferation of human breast cancer cell lines in vitro and in vivo is well documented. However, the molecular mechanisms have not been fully elucidated. In the present study, MDA-MB-231 cells were treated with different concentrations of Tan-IIA for 48 h, followed by protein extraction for western blotting. For an in vivo study, MDA-MB-231 cells were implanted directly into female SCID mice which were divided randomly into three groups to be treated with vehicle, Tan-IIA (20 mg/kg) and Tan-IIA (60 mg/kg) every other day orally, with treatment starting 4 weeks after inoculation with the MDA-MB-231 cells. The results showed that Tan-IIA inhibited the proliferation of MDA-MB-231 cells and decreased the protein expression of LC3-II and Erb-B2 in vitro. Treatment with Tan-IIA (20 or 60 mg/kg) for 90 days resulted in a reduction in tumor size and weight compared to the control group. The protein expression of NF-κBp65 was reduced, while caspase-3 was up-regulated compared to the control group. These findings indicate that Tan-IIA inhibits tumor growth in a MDA-MB-231 xenograft animal model. One of the molecular mechanisms may be through a decrease in NF-κBp65 and an increase in caspase-3 expression.
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Copy and paste a formatted citation
Spandidos Publications style
Su C, Chien S, Kuo S, Chen Y, Cheng C and Chen D: Tanshinone IIA inhibits human breast cancer MDA-MB-231 cells by decreasing LC3-II, Erb-B2 and NF-κBp65. Mol Med Rep 5: 1019-1022, 2012.
APA
Su, C., Chien, S., Kuo, S., Chen, Y., Cheng, C., & Chen, D. (2012). Tanshinone IIA inhibits human breast cancer MDA-MB-231 cells by decreasing LC3-II, Erb-B2 and NF-κBp65. Molecular Medicine Reports, 5, 1019-1022. https://doi.org/10.3892/mmr.2012.756
MLA
Su, C., Chien, S., Kuo, S., Chen, Y., Cheng, C., Chen, D."Tanshinone IIA inhibits human breast cancer MDA-MB-231 cells by decreasing LC3-II, Erb-B2 and NF-κBp65". Molecular Medicine Reports 5.4 (2012): 1019-1022.
Chicago
Su, C., Chien, S., Kuo, S., Chen, Y., Cheng, C., Chen, D."Tanshinone IIA inhibits human breast cancer MDA-MB-231 cells by decreasing LC3-II, Erb-B2 and NF-κBp65". Molecular Medicine Reports 5, no. 4 (2012): 1019-1022. https://doi.org/10.3892/mmr.2012.756
Copy and paste a formatted citation
x
Spandidos Publications style
Su C, Chien S, Kuo S, Chen Y, Cheng C and Chen D: Tanshinone IIA inhibits human breast cancer MDA-MB-231 cells by decreasing LC3-II, Erb-B2 and NF-κBp65. Mol Med Rep 5: 1019-1022, 2012.
APA
Su, C., Chien, S., Kuo, S., Chen, Y., Cheng, C., & Chen, D. (2012). Tanshinone IIA inhibits human breast cancer MDA-MB-231 cells by decreasing LC3-II, Erb-B2 and NF-κBp65. Molecular Medicine Reports, 5, 1019-1022. https://doi.org/10.3892/mmr.2012.756
MLA
Su, C., Chien, S., Kuo, S., Chen, Y., Cheng, C., Chen, D."Tanshinone IIA inhibits human breast cancer MDA-MB-231 cells by decreasing LC3-II, Erb-B2 and NF-κBp65". Molecular Medicine Reports 5.4 (2012): 1019-1022.
Chicago
Su, C., Chien, S., Kuo, S., Chen, Y., Cheng, C., Chen, D."Tanshinone IIA inhibits human breast cancer MDA-MB-231 cells by decreasing LC3-II, Erb-B2 and NF-κBp65". Molecular Medicine Reports 5, no. 4 (2012): 1019-1022. https://doi.org/10.3892/mmr.2012.756
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