The phosphoinositide 3-kinase/AKT1 pathway involvement in drug and all-trans-retinoic acid resistance of leukemia cells

Mol Cancer Res. 2003 Jan;1(3):234-46.

Abstract

Disruption of the apoptotic pathways may account for resistance to chemotherapy and treatment failures in human neoplastic disease. To further evaluate this issue, we isolated a HL-60 cell clone highly resistant to several drugs inducing apoptosis and to the differentiating chemical all-trans-retinoic acid (ATRA). The resistant clone displayed an activated phosphoinositide 3-kinase (PI3K)/AKT1 pathway, with levels of phosphatidylinositol (3,4,5) trisphosphate higher than the parental cells and increased levels of both Thr 308 and Ser 473 phosphorylated AKT1. In vitro AKT1 activity was elevated in resistant cells, whereas treatment of the resistant cell clone with two inhibitors of PI3K, wortmannin or Ly294002, strongly reduced phosphatidylinositol (3,4,5) trisphosphate levels and AKT1 activity. The inhibitors reversed resistance to drugs. Resistant cells overexpressing either dominant negative PI3K or dominant negative AKT1 became sensitive to drugs and ATRA. Conversely, if parental HL-60 cells were forced to overexpress an activated AKT1, they became resistant to apoptotic inducers and ATRA. There was a tight relationship between the activation of the PI3K/AKT1 axis and the expression of c-IAP1 and c-IAP2 proteins. Activation of the PI3K/AKT1 axis in resistant cells was dependent on enhanced tyrosine phosphorylation of the p85 regulatory subunit of PI3K, conceivably due to an autocrine insulin-like growth factor-I production. Our findings suggest that an up-regulation of the PI3K/AKT1 pathway might be one of the survival mechanisms responsible for the onset of resistance to chemotherapeutic and differentiating therapy in patients with acute leukemia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Apoptosis / drug effects
  • Carrier Proteins / metabolism
  • Drug Resistance, Neoplasm / physiology*
  • Gene Expression Regulation, Leukemic
  • HL-60 Cells
  • Humans
  • Inhibitor of Apoptosis Proteins
  • Insulin-Like Growth Factor I / metabolism
  • Leukemia, Promyelocytic, Acute*
  • PTEN Phosphohydrolase
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Phosphoric Monoester Hydrolases / metabolism
  • Phosphorylation
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • Proteins / genetics
  • Proto-Oncogene Proteins c-akt
  • Proto-Oncogene Proteins*
  • Ribosomal Protein S6 Kinases, 70-kDa / metabolism
  • Transfection
  • Tretinoin / pharmacology*
  • Tumor Suppressor Proteins / metabolism
  • Ubiquitin-Protein Ligases
  • bcl-Associated Death Protein

Substances

  • Antineoplastic Agents
  • BAD protein, human
  • Carrier Proteins
  • Inhibitor of Apoptosis Proteins
  • Proteins
  • Proto-Oncogene Proteins
  • Tumor Suppressor Proteins
  • bcl-Associated Death Protein
  • Tretinoin
  • Insulin-Like Growth Factor I
  • BIRC2 protein, human
  • Ubiquitin-Protein Ligases
  • AKT1 protein, human
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt
  • Ribosomal Protein S6 Kinases, 70-kDa
  • Phosphoric Monoester Hydrolases
  • PTEN Phosphohydrolase
  • PTEN protein, human