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Article

BMP9 inhibits the growth of breast cancer cells by downregulation of the PI3K/Akt signaling pathway

  • Authors:
    • Shu Li
    • Hongying Dai
    • Yong He
    • Shusheng Peng
    • Tianjin Zhu
    • Yang Wu
    • Chenwei Li
    • Ke Wang
  • View Affiliations / Copyright

    Affiliations: Clinical Laboratory, Yongchuan Hospital of Chongqing Medical University, Chongqing 402160, P.R. China, Clinical Laboratory, Yongchuan Hospital of Chongqing Medical University, Chongqing 402160, P.R. China, Yubei District People's Hospital of Chongqing, Chongqing 401120, P.R. China
  • Pages: 1743-1751
    |
    Published online on: July 13, 2018
       https://doi.org/10.3892/or.2018.6572
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Abstract

Bone morphogenetic protein 9 (BMP9) is a member of the BMP family, which is involved in the regulation of tumor biogenesis, development and metastasis. The present study aimed to investigate whether BMP9 inhibits the growth of MDA‑MB‑231 breast cancer cells via the phosphoinositide 3‑kinase (PI3K)/Akt signaling pathway. It was shown that the expression level of BMP9 was significantly decreased, while that of phosphorylated Akt (p‑Akt) was markedly increased in breast cancer tissues compared with these levels in the normal adjacent tissues. An adenovirus overexpressing BMP9 was used to infect the MDA‑MB‑231 cells. The expression level of p‑Akt in the MDA‑MB‑231/BMP9 group was shown to be significantly lower than that in the MDA‑MB‑231/green fluorescent protein (GFP) and MDA‑MB‑231 control groups. The expression levels of cyclins D1, B1 and E1, c‑Myc and matrix metalloproteinase 9 (MMP9) in the MDA‑MB‑231/BMP9 group were also reduced. The generation of a nude mouse xenograft tumor model revealed that the tumor volumes of the MDA‑MB‑231/BMP9 group (0.32±0.05 cm3) was significantly lower compared with that of the MDA‑MB‑231/GFP (1.10±0.05 cm3) and MDA‑MB‑231 (1.12±0.12 cm3) groups, and the expression level of p‑Akt protein in the MDA‑MB‑231/BMP9 group was significantly lower compared with that of the MDA‑MB‑231/GFP and MDA‑MB‑231 groups in the nude mouse xenograft model. Taken together, these results indicate that BMP9 inhibits the growth of MDA‑MB‑231 breast cancer cells by inhibiting the PI3K/Akt signaling pathway both in vivo and in vitro.
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Copy and paste a formatted citation
Spandidos Publications style
Li S, Dai H, He Y, Peng S, Zhu T, Wu Y, Li C and Wang K: BMP9 inhibits the growth of breast cancer cells by downregulation of the PI3K/Akt signaling pathway. Oncol Rep 40: 1743-1751, 2018.
APA
Li, S., Dai, H., He, Y., Peng, S., Zhu, T., Wu, Y. ... Wang, K. (2018). BMP9 inhibits the growth of breast cancer cells by downregulation of the PI3K/Akt signaling pathway. Oncology Reports, 40, 1743-1751. https://doi.org/10.3892/or.2018.6572
MLA
Li, S., Dai, H., He, Y., Peng, S., Zhu, T., Wu, Y., Li, C., Wang, K."BMP9 inhibits the growth of breast cancer cells by downregulation of the PI3K/Akt signaling pathway". Oncology Reports 40.3 (2018): 1743-1751.
Chicago
Li, S., Dai, H., He, Y., Peng, S., Zhu, T., Wu, Y., Li, C., Wang, K."BMP9 inhibits the growth of breast cancer cells by downregulation of the PI3K/Akt signaling pathway". Oncology Reports 40, no. 3 (2018): 1743-1751. https://doi.org/10.3892/or.2018.6572
Copy and paste a formatted citation
x
Spandidos Publications style
Li S, Dai H, He Y, Peng S, Zhu T, Wu Y, Li C and Wang K: BMP9 inhibits the growth of breast cancer cells by downregulation of the PI3K/Akt signaling pathway. Oncol Rep 40: 1743-1751, 2018.
APA
Li, S., Dai, H., He, Y., Peng, S., Zhu, T., Wu, Y. ... Wang, K. (2018). BMP9 inhibits the growth of breast cancer cells by downregulation of the PI3K/Akt signaling pathway. Oncology Reports, 40, 1743-1751. https://doi.org/10.3892/or.2018.6572
MLA
Li, S., Dai, H., He, Y., Peng, S., Zhu, T., Wu, Y., Li, C., Wang, K."BMP9 inhibits the growth of breast cancer cells by downregulation of the PI3K/Akt signaling pathway". Oncology Reports 40.3 (2018): 1743-1751.
Chicago
Li, S., Dai, H., He, Y., Peng, S., Zhu, T., Wu, Y., Li, C., Wang, K."BMP9 inhibits the growth of breast cancer cells by downregulation of the PI3K/Akt signaling pathway". Oncology Reports 40, no. 3 (2018): 1743-1751. https://doi.org/10.3892/or.2018.6572
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