[Effects of HO-1 gene expression on proliferation of imatinib resistant CML cells]

Ji-Shi Wang1, Bai-Sheng Chai, Qin Fang

  • 1Department of Hematology, Affiliated Hospital of Gui Yang Medical College, Guiyang 550004, China.

Abstract

Insights

Heme oxygenase-1 (HO-1) promotes the growth of imatinib-resistant chronic myeloid leukemia (CML) cells. Inhibiting HO-1 expression offers a potential therapeutic strategy for drug-resistant CML.

Area of Science:

  • Hematology
  • Molecular Biology
  • Cancer Research

Background:

  • Imatinib resistance is a significant challenge in treating chronic myeloid leukemia (CML).
  • Heme oxygenase-1 (HO-1) is an enzyme involved in cellular stress responses.
  • The role of HO-1 in drug-resistant CML remains to be fully elucidated.

Purpose of the Study:

  • To investigate the effect of HO-1 expression on cell growth and apoptosis in imatinib-resistant CML cells (K562/A02-IM).
  • To explore the relationship between the HO-1 gene and CML progression and drug resistance.

Main Methods:

  • Detected HO-1 expression in drug-resistant CML patients using RT-PCR.
  • Induced HO-1 expression in K562/A02-IM cells with hemin and analyzed expression levels via RT-PCR and Western blot.
  • Assessed cell apoptosis using Annexin V/PI staining and cell viability using MTT assay after HO-1 modulation.

Main Results:

  • HO-1 was expressed in bone marrow mononuclear cells (BMMNCs) of CML patients.
  • Hemin treatment dose-dependently increased HO-1 expression and induced apoptosis in K562/A02-IM cells.
  • HO-1 induction promoted K562/A02-IM cell survival, while inhibition with zinc protoporphyrin (ZPP) significantly decreased cell survival.

Conclusions:

  • HO-1 is expressed in BMMNCs and its induction promotes the growth of drug-resistant CML cells.
  • HO-1 acts as a survival factor in imatinib-resistant CML.
  • Inhibition of HO-1 presents a potential therapeutic approach for treating drug-resistant CML.

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