4.7 Article

Tipifarnib sensitizes cells to proteasome inhibition by blocking degradation of bortezomib-induced aggresomes

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BLOOD
卷 116, 期 24, 页码 5285-5288

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AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2010-03-272393

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  1. Winship Cancer Institute of Emory University
  2. Leukemia & Lymphoma Society
  3. Multiple Myeloma Research Foundation
  4. Millennium
  5. Celgene
  6. Bristol-Myers Squibb
  7. Novartis
  8. Merck

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In this report, we investigated the mechanism responsible for synergistic induction of myeloma cell apoptosis induced by the combination of tipifarnib and bortezomib. Immunofluorescence studies revealed that bortezomib alone resulted in an accumulation of puncta of ubiquitinated proteins that was further enhanced by the addition of tipifarnib. These data suggest inhibition of the degradation of bortezomib-induced aggresomes; and consistent with this possibility, we also observed an increase in p62SQSTM1 in cells treated with the combination. However, autophagy in these cells appears to be normal as LC3BII is present, and auto-phagic flux appears to be unaffected as demonstrated by the addition of bafilomycin A(1). Together, these data demonstrate that tipifarnib synergizes with bortezomib by inducing protein accumulation as a result of the uncoupling of the aggresome and autophagy pathways. (Blood. 2010;116(24):5285-5288)

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