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February 2013 Volume 7 Issue 2

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Article

Application of platelet-rich plasma accelerates the wound healing process in acute and chronic ulcers through rapid migration and upregulation of cyclin A and CDK4 in HaCaT cells

  • Authors:
    • Sung-Ae Kim
    • Han-Won Ryu
    • Kyu-Suk Lee
    • Jae-We Cho
  • View Affiliations / Copyright

    Affiliations: Department of Dermatology, Keimyung University School of Medicine, Daegu 700-712, Republic of Korea
  • Pages: 476-480
    |
    Published online on: December 12, 2012
       https://doi.org/10.3892/mmr.2012.1230
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Abstract

Application of autologous platelet-rich plasma (PRP) has been used for chronic wound healing. The aim of this study was to evaluate the effect of PRP on the wound healing processes of both acute and chronic ulcers and the underlying molecular mechanisms involved. We treated 16 patients affected by various acute and chronic ulcers with PRP. We performed molecular studies of cell proliferation, migration assays, immunoblotting and chloramphenicol acetyltransferase (CAT) assays in PRP-treated HaCaT keratinocyte cells. PRP treatment induced increased rates of cell proliferation and cell migration of HaCaT cells. In addition, the expression of cyclin A and cyclin dependent kinase (CDK) 4 proteins was markedly increased with a low concentration (0.5%) of PRP treatment in HaCaT cells. In 11 patients with chronic ulcers, including stasis ulcers, diabetic ulcers, venous leg ulcers, livedoid vasculitis, claw foot and traumatic ulcers, 9 patients showed 90-100% epithelization after 15.18 days. In 5 patients with acute ulcers, such as dehiscence, open wound and burn wound, 80-100% epithelization was achieved between 4 to 20 days. Topical application of PRP to acute and chronic skin ulcers significantly accelerated the epithelization process, likely through upregulation of the cell cycle regulatory proteins cyclin A and CDK4.
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Copy and paste a formatted citation
Spandidos Publications style
Kim S, Ryu H, Lee K and Cho J: Application of platelet-rich plasma accelerates the wound healing process in acute and chronic ulcers through rapid migration and upregulation of cyclin A and CDK4 in HaCaT cells. Mol Med Rep 7: 476-480, 2013.
APA
Kim, S., Ryu, H., Lee, K., & Cho, J. (2013). Application of platelet-rich plasma accelerates the wound healing process in acute and chronic ulcers through rapid migration and upregulation of cyclin A and CDK4 in HaCaT cells. Molecular Medicine Reports, 7, 476-480. https://doi.org/10.3892/mmr.2012.1230
MLA
Kim, S., Ryu, H., Lee, K., Cho, J."Application of platelet-rich plasma accelerates the wound healing process in acute and chronic ulcers through rapid migration and upregulation of cyclin A and CDK4 in HaCaT cells". Molecular Medicine Reports 7.2 (2013): 476-480.
Chicago
Kim, S., Ryu, H., Lee, K., Cho, J."Application of platelet-rich plasma accelerates the wound healing process in acute and chronic ulcers through rapid migration and upregulation of cyclin A and CDK4 in HaCaT cells". Molecular Medicine Reports 7, no. 2 (2013): 476-480. https://doi.org/10.3892/mmr.2012.1230
Copy and paste a formatted citation
x
Spandidos Publications style
Kim S, Ryu H, Lee K and Cho J: Application of platelet-rich plasma accelerates the wound healing process in acute and chronic ulcers through rapid migration and upregulation of cyclin A and CDK4 in HaCaT cells. Mol Med Rep 7: 476-480, 2013.
APA
Kim, S., Ryu, H., Lee, K., & Cho, J. (2013). Application of platelet-rich plasma accelerates the wound healing process in acute and chronic ulcers through rapid migration and upregulation of cyclin A and CDK4 in HaCaT cells. Molecular Medicine Reports, 7, 476-480. https://doi.org/10.3892/mmr.2012.1230
MLA
Kim, S., Ryu, H., Lee, K., Cho, J."Application of platelet-rich plasma accelerates the wound healing process in acute and chronic ulcers through rapid migration and upregulation of cyclin A and CDK4 in HaCaT cells". Molecular Medicine Reports 7.2 (2013): 476-480.
Chicago
Kim, S., Ryu, H., Lee, K., Cho, J."Application of platelet-rich plasma accelerates the wound healing process in acute and chronic ulcers through rapid migration and upregulation of cyclin A and CDK4 in HaCaT cells". Molecular Medicine Reports 7, no. 2 (2013): 476-480. https://doi.org/10.3892/mmr.2012.1230
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