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Article

Dasatinib inhibits primary melanoma cell proliferation through morphology‑dependent disruption of Src‑ERK signaling

  • Authors:
    • Jianghong Wu
    • Xin Liao
    • Bo Yu
    • Bing Su
  • View Affiliations / Copyright

    Affiliations: Department of Gastric Cancer and Soft Tissue Sarcoma Surgery, Fudan University Shanghai Cancer Center, Shanghai 200032, P.R. China, Biomedical Research Institute, Shenzhen-PKU-HKUST Medical Center, Futian, Shenzhen, Guangdong 518036, P.R. China, Department of Dermatology, Peking University Shenzhen Hospital, Futian, Shenzhen, Guangdong 518036, P.R. China
  • Pages: 527-532
    |
    Published online on: December 10, 2012
       https://doi.org/10.3892/ol.2012.1066
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Abstract

New strategies for the treatment of advanced melanoma are urgently required. The RAS/RAF/MAPK pathway and c‑Src are deregulated in the majority of malignant melanomas, suggesting that they may interact functionally and are involved in the development and progression of the malignancy. Preclinical studies have demonstrated variable inhibition of melanoma cell growth by dasatinib in vitro. Src may act through different downstream signaling pathways. In the present study, we demonstrate that dasatinib induces changes in cell morphology, characterized by an arborized and contracted appearance, and accompanied by a reduction in cell proliferation in primary melanoma cells. This morphological change is demonstrated to be associated with the inhibition of nuclear translocation of activated ERK1/2. Together, these results indicate that Src may promote cell proliferation through the activation of the ERK signaling pathway in melanoma oncogenesis.
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Copy and paste a formatted citation
Spandidos Publications style
Wu J, Liao X, Yu B and Su B: Dasatinib inhibits primary melanoma cell proliferation through morphology‑dependent disruption of Src‑ERK signaling. Oncol Lett 5: 527-532, 2013.
APA
Wu, J., Liao, X., Yu, B., & Su, B. (2013). Dasatinib inhibits primary melanoma cell proliferation through morphology‑dependent disruption of Src‑ERK signaling. Oncology Letters, 5, 527-532. https://doi.org/10.3892/ol.2012.1066
MLA
Wu, J., Liao, X., Yu, B., Su, B."Dasatinib inhibits primary melanoma cell proliferation through morphology‑dependent disruption of Src‑ERK signaling". Oncology Letters 5.2 (2013): 527-532.
Chicago
Wu, J., Liao, X., Yu, B., Su, B."Dasatinib inhibits primary melanoma cell proliferation through morphology‑dependent disruption of Src‑ERK signaling". Oncology Letters 5, no. 2 (2013): 527-532. https://doi.org/10.3892/ol.2012.1066
Copy and paste a formatted citation
x
Spandidos Publications style
Wu J, Liao X, Yu B and Su B: Dasatinib inhibits primary melanoma cell proliferation through morphology‑dependent disruption of Src‑ERK signaling. Oncol Lett 5: 527-532, 2013.
APA
Wu, J., Liao, X., Yu, B., & Su, B. (2013). Dasatinib inhibits primary melanoma cell proliferation through morphology‑dependent disruption of Src‑ERK signaling. Oncology Letters, 5, 527-532. https://doi.org/10.3892/ol.2012.1066
MLA
Wu, J., Liao, X., Yu, B., Su, B."Dasatinib inhibits primary melanoma cell proliferation through morphology‑dependent disruption of Src‑ERK signaling". Oncology Letters 5.2 (2013): 527-532.
Chicago
Wu, J., Liao, X., Yu, B., Su, B."Dasatinib inhibits primary melanoma cell proliferation through morphology‑dependent disruption of Src‑ERK signaling". Oncology Letters 5, no. 2 (2013): 527-532. https://doi.org/10.3892/ol.2012.1066
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