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International Journal of Molecular Medicine
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Article

SIPL1 enhances the proliferation, attachment, and migration of CHO cells by inhibiting PTEN function

  • Authors:
    • Jason De Melo
    • Vincent Wu
    • Lizhi He
    • Judy Yan
    • Damu Tang
  • View Affiliations / Copyright

    Affiliations: Division of Nephrology, Department of Medicine, McMaster University, Hamilton, ON L8N 4A6, Canada
  • Pages: 835-841
    |
    Published online on: July 8, 2014
       https://doi.org/10.3892/ijmm.2014.1840
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Abstract

The PTEN tumour suppressor plays critical roles in inhibiting cell proliferation, adhesion and migration through downregulation of the PI3K-AKT pathway. SIPL1 is a novel PTEN‑negative regulator (PTEN-NR) that contributes to PTEN inactivation during tumorigenesis. However, whether SIPL1 plays a role in inhibiting PTEN function in the process of cell adhesion and migration remains unclear. The aim of this study was to investigate this possibility using CHO-K1 cells, and western blotting, qPCR analyses and microscopy. Results showed that the overexpression of SIPL1 in CHO-K1 cells decreased the amount of PTEN protein. The downregulation was not caused by an obvious reduction in PTEN mRNA levels or ubiquitin-dependent protein degradation. Nonetheless, the reduction was functional, as SIPL1 overexpression increased the activation of AKT under serum‑starved conditions, promoting CHO-K1 cell proliferation in an AKT‑dependent manner. Furthermore, SIPL1 increased the migration and attachment of CHO-K1 cells. Taken together, the evidence suggested that SIPL1 promotes AKT activation by decreasing the amount of PTEN protein in CHO-K1 cells, thereby promoting cell proliferation and migration.
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Copy and paste a formatted citation
Spandidos Publications style
De Melo J, Wu V, He L, Yan J and Tang D: SIPL1 enhances the proliferation, attachment, and migration of CHO cells by inhibiting PTEN function. Int J Mol Med 34: 835-841, 2014.
APA
De Melo, J., Wu, V., He, L., Yan, J., & Tang, D. (2014). SIPL1 enhances the proliferation, attachment, and migration of CHO cells by inhibiting PTEN function. International Journal of Molecular Medicine, 34, 835-841. https://doi.org/10.3892/ijmm.2014.1840
MLA
De Melo, J., Wu, V., He, L., Yan, J., Tang, D."SIPL1 enhances the proliferation, attachment, and migration of CHO cells by inhibiting PTEN function". International Journal of Molecular Medicine 34.3 (2014): 835-841.
Chicago
De Melo, J., Wu, V., He, L., Yan, J., Tang, D."SIPL1 enhances the proliferation, attachment, and migration of CHO cells by inhibiting PTEN function". International Journal of Molecular Medicine 34, no. 3 (2014): 835-841. https://doi.org/10.3892/ijmm.2014.1840
Copy and paste a formatted citation
x
Spandidos Publications style
De Melo J, Wu V, He L, Yan J and Tang D: SIPL1 enhances the proliferation, attachment, and migration of CHO cells by inhibiting PTEN function. Int J Mol Med 34: 835-841, 2014.
APA
De Melo, J., Wu, V., He, L., Yan, J., & Tang, D. (2014). SIPL1 enhances the proliferation, attachment, and migration of CHO cells by inhibiting PTEN function. International Journal of Molecular Medicine, 34, 835-841. https://doi.org/10.3892/ijmm.2014.1840
MLA
De Melo, J., Wu, V., He, L., Yan, J., Tang, D."SIPL1 enhances the proliferation, attachment, and migration of CHO cells by inhibiting PTEN function". International Journal of Molecular Medicine 34.3 (2014): 835-841.
Chicago
De Melo, J., Wu, V., He, L., Yan, J., Tang, D."SIPL1 enhances the proliferation, attachment, and migration of CHO cells by inhibiting PTEN function". International Journal of Molecular Medicine 34, no. 3 (2014): 835-841. https://doi.org/10.3892/ijmm.2014.1840
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