Tumor necrosis factor alpha is a powerful apoptotic inducer in lymphoid leukemic cells expressing the P-170 glycoprotein

Int J Cancer. 1996 Jul 17;67(2):238-47. doi: 10.1002/(SICI)1097-0215(19960717)67:2<238::AID-IJC15>3.0.CO;2-7.

Abstract

Multidrug resistance (MDR) is a phenomenon by which tumor cells exposed to a single anti-proliferative agent acquire resistance to other structurally and functionally unrelated drugs. The classical form of MDR is caused by a plasma-membrane protein currently named P-glycoprotein or P-170 encoded by the human mdr-1 gene in its functional isoform. In vitro cell lines expressing P-170 usually also present phenotypic and functional alterations. In the present study we report that the cytotoxicity mediated by tumor necrosis factor alpha (TNF alpha) in MDR variants of the human T-lymphoblastoid CEM cell line is associated with apoptosis (programmed cell death). Susceptibility of MDR cells to apoptosis was increased upon cycloheximide + TNF alpha sequential treatment, whereby the impairment of protein synthesis due to the former agent was followed by the effect of cytokine exposure. Massive apoptosis of P-170-positive cells, but not of controls, was also obtained by depletion of nutrients (i.e., serum starvation). In contrast, TNF-alpha exerted a similar apoptotic effect in epithelial (MCF-7) or myeloma (S8226) drug-sensitive/ -resistant cell pairs. However, the MDR variant of myeloma S8226 was more sensitive to the cytostatic effect of TNF alpha than the parental drug-sensitive cell line. These results suggest that the presence of the MDR phenotype may be associated with increased histotype-dependent cell susceptibility to specific, protein-synthesis-independent, apoptotic pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / analysis*
  • Apoptosis*
  • Cell Division
  • Cycloheximide / pharmacology
  • Drug Resistance, Multiple*
  • Flow Cytometry
  • Fluorescent Antibody Technique
  • Humans
  • Leukemia, Lymphoid / metabolism*
  • Leukemia, Lymphoid / pathology*
  • Microscopy, Fluorescence
  • Phenotype
  • Protein Synthesis Inhibitors / pharmacology
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Protein Synthesis Inhibitors
  • Tumor Necrosis Factor-alpha
  • Cycloheximide