The antidepressant sertraline downregulates Akt and has activity against melanoma cells

Summary Melanoma is a common malignancy which is poorly responsive to chemotherapy and radiation. One of the major reasons melanoma responds poorly to these modalities is constitutive expression of Akt, which protects against apoptosis. The antidepressant sertraline was found to be a potent cytotoxi...

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Published inPigment cell and melanoma research Vol. 21; no. 4; pp. 451 - 456
Main Authors Reddy, Kalpana K., Lefkove, Benjamin, Chen, Lan Bo, Govindarajan, Baskaran, Carracedo, Arkaitz, Velasco, Guillermo, Carrillo, Carol O., Bhandarkar, Sulochana S., Owens, Michael J., Mechta-Grigoriou, Fatima, Arbiser, Jack L.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.08.2008
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Summary:Summary Melanoma is a common malignancy which is poorly responsive to chemotherapy and radiation. One of the major reasons melanoma responds poorly to these modalities is constitutive expression of Akt, which protects against apoptosis. The antidepressant sertraline was found to be a potent cytotoxic agent against A375 human melanoma. To determine the mechanism by which sertraline kills melanoma cells, Western blot analysis of signaling molecules, including phosphorylated Akt, caspase 9 and phospho‐p70 S6 kinase was performed. Finally, the effects of sertraline on A375 xenografts in mice were assessed. Sertaline potently inhibited the phosphorylation of Akt, and caused cell death through induction of endoplasmic reticulum in vitro. Sertraline monotherapy demonstrated activity against A375 xenografts in vivo. Akt is a major cause of resistance of melanoma to current therapy. Antidepressants are commonly used to prevent interferon‐induced depression. Use of antidepressants that decrease Akt may improve the efficacy of interferon and other therapies against melanoma. Further studies are needed to elucidate whether sertraline acts as an Akt inhibitor in melanoma.
Bibliography:ark:/67375/WNG-Q4KM5ZMV-C
ArticleID:PCMR481
istex:DAF46A3F3017D5712124D53F99E8515B2BDCBD38
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1755-1471
1755-148X
DOI:10.1111/j.1755-148X.2008.00481.x