Aldehyde-dehydrogenase gene-transduced hematopoietic cell line K562 overcomes the cytoxicity of cyclophosphamide in vitro

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2002 Jun;10(3):205-8.

Abstract

The identification of genes inducing resistance to anticancer chemotherapeutic agents and their introduction into hematopoietic cells represents a promising approach to overcome bone marrow toxicity, the limiting factor for most high-dose chemotherapy regimens. Because resistance to cyclophosphamide has been correlated with increased levels of expression of the aldehyde-dehydrogenase (ALDH1) gene in tumor cells lines in vitro, this study tested whether ALDH1 overexpression could directly induce cyclophosphamide resistance. Results showed that a retroviral vector was used to transduce full-length human ALDH1 cDNA into human hematopoietic cell line K562 that was then tested for resistance to 4-hydroxycyclophosphamide (4-HC), an active analogue of cyclophosphamide. Overexpression of the ALDH1 gene resulted in a significant increases in cyclophosphamide resistance in transduced K562 cells (50% inhibition concentration, IC50 = 10 micro mol/L). These findings indicate that ALDH1 overexpression is sufficient to induce cyclophosphamide resistance in vitro and provide a basis for testing the efficacy of ALDH1 gene transduction to protect bone marrow cells from high-dose cyclophosphamide in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehyde Dehydrogenase / genetics*
  • Antineoplastic Agents, Alkylating / pharmacology*
  • Cell Division / drug effects
  • Cell Survival / drug effects*
  • Cyclophosphamide / analogs & derivatives*
  • Cyclophosphamide / pharmacology*
  • Dose-Response Relationship, Drug
  • Drug Resistance, Neoplasm
  • Gene Expression Regulation, Enzymologic
  • Genetic Vectors / genetics
  • Humans
  • Inhibitory Concentration 50
  • K562 Cells / drug effects*
  • K562 Cells / enzymology
  • K562 Cells / metabolism
  • Retroviridae / genetics
  • Transfection

Substances

  • Antineoplastic Agents, Alkylating
  • 4-hydroxycyclophosphamide
  • Cyclophosphamide
  • Aldehyde Dehydrogenase