Bisphosphonate incadronate inhibits growth of human T-cell leukaemia virus type I-infected T-cell lines and primary adult T-cell leukaemia cells by interfering with the mevalonate pathway

Br J Haematol. 2007 Feb;136(3):424-32. doi: 10.1111/j.1365-2141.2006.06445.x.

Abstract

Anti-resorptive bisphosphonates are used for the treatment of hypercalcaemia and bone complications associated with malignancies and osteoporosis, but also have been shown to have anti-tumour effects in various cancers. Adult T-cell leukaemia (ATL) is a fatal T-cell malignancy caused by infection with human T-cell leukaemia virus type I (HTLV-I), and remains incurable. ATL is associated with osteolytic bone lesions and hypercalcaemia, both of which are major factors in the morbidity of ATL. Thus, the search for anti-ATL agents that have both anti-tumour and anti-resorptive activity is warranted. The bisphosphonate agent, incadronate, prevented cell growth of HTLV-I-infected T-cell lines and primary ATL cells, but not of non-infected T-cell lines or normal peripheral blood mononuclear cells. Incadronate induced S-phase cell cycle arrest and apoptosis in HTLV-I-infected T-cell lines, and treatment of these cells with substrates of the mevalonate pathway blocked the incadronate-mediated growth suppression. Incadronate also prevented the prenylation of Rap1A protein. These results demonstrated that incadronate-induced growth suppression occurs by interfering with the mevalonate pathway. Importantly, treatment with incadronate reduced tumour formation from an HTLV-I-infected T-cell line when these cells were inoculated subcutaneously into severe combined immunodeficient mice. These findings suggest that incadronate could be potentially useful for the treatment of ATL.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Animals
  • Antimetabolites / pharmacology
  • Antimetabolites / therapeutic use*
  • Apoptosis / drug effects
  • Biomarkers / analysis
  • Blotting, Western / methods
  • Caspases / metabolism
  • Cell Cycle / drug effects
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Diphosphonates / pharmacology
  • Diphosphonates / therapeutic use*
  • Female
  • Human T-lymphotropic virus 1*
  • Humans
  • Inhibitor of Apoptosis Proteins
  • Jurkat Cells
  • Leukemia, T-Cell / drug therapy*
  • Leukemia, T-Cell / metabolism
  • Leukemia-Lymphoma, Adult T-Cell / drug therapy
  • Leukemia-Lymphoma, Adult T-Cell / metabolism
  • Male
  • Mevalonic Acid / metabolism*
  • Mice
  • Mice, SCID
  • Microtubule-Associated Proteins / analysis
  • Microtubule-Associated Proteins / metabolism
  • Middle Aged
  • Neoplasm Proteins / analysis
  • Neoplasm Proteins / metabolism
  • Neoplasm Transplantation
  • Signal Transduction / drug effects
  • Survivin
  • T-Lymphocytes / metabolism*
  • T-Lymphocytes / virology

Substances

  • Antimetabolites
  • BIRC5 protein, human
  • Biomarkers
  • Diphosphonates
  • Inhibitor of Apoptosis Proteins
  • Microtubule-Associated Proteins
  • Neoplasm Proteins
  • Survivin
  • cimadronate
  • Caspases
  • Mevalonic Acid