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Efficient lysis of B-chronic lymphocytic leukemia cells by the plant-derived sesquiterpene alcohol α-bisabolol, a dual proapoptotic and antiautophagic agent.
Rigo, Antonella; Ferrarini, Isacco; Bonalumi, Angela; Tecchio, Cristina; Montresor, Alessio; Laudanna, Carlo; Vinante, Fabrizio.
Afiliação
  • Rigo A; Section of Hematology, Department of Medicine, University of Verona, Verona, Italy.
  • Ferrarini I; Cancer Research and Cell Biology Laboratory, Department of Medicine, University of Verona, Verona, Italy.
  • Bonalumi A; Section of Hematology, Department of Medicine, University of Verona, Verona, Italy.
  • Tecchio C; Cancer Research and Cell Biology Laboratory, Department of Medicine, University of Verona, Verona, Italy.
  • Montresor A; Section of Hematology, Department of Medicine, University of Verona, Verona, Italy.
  • Laudanna C; Section of Hematology, Department of Medicine, University of Verona, Verona, Italy.
  • Vinante F; Section of General Pathology, Department of Medicine, University of Verona, Verona, Italy.
Oncotarget ; 9(40): 25877-25890, 2018 May 25.
Article em En | MEDLINE | ID: mdl-29899828
ABSTRACT
The sesquiterpene α-bisabolol (α-BSB) is a cytotoxic agent against acute leukemia and chronic myeloid leukemia cells. Here the profile of α-BSB citotoxicity was evaluated ex vivo in primary mononuclear blood cells isolated from 45 untreated B-chronic lymphocytic leukemia (B-CLL) patients. We studied the effects of α-BSB by flow cytometric and western blotting techniques with the following

findings:

(1) α-BSB was an effective proapoptotic agent against B-CLL cells (IC50 42 ± 15 µM). It was also active, but to a lesser extent, on normal residual B cells and monocytes (IC50 68 ± 34 and 74 ± 28 µM, respectively; p < 0.01), while T-cells, though not achieving IC50, were nevertheless decreased. (2) Lipid raft content positively correlated with α-BSB cell sensitivity, while neither the phenotype of B-CLL cells nor the disease clinical stage did affect the sensitivity to α-BSB. (3) Flow cytometry analysis evidenced the induction of pores in mitochondrial and lysosomal membrane after 3- to 5-hour exposure of B-CLL cells to α-BSB, leading to apoptosis; in contrast, western blotting analysis showed inhibition of the autophagic flux. Therefore, according to cellular selectivity, α-BSB is a cytotoxic agent preferentially active against leukemic cells, while its lower activity on normal B cells, monocytes and T cells may account for an additive anti-inflammatory effect targeting the leukemia-associated pro-inflammatory microenvironment. Consistent with the observed effects on intracellular processes, α-BSB should be regarded as a dual agent, both activating mitochondrial-based apoptosis and inhibiting autophagy by disrupting lysosomes.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Oncotarget Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Oncotarget Ano de publicação: 2018 Tipo de documento: Article