Rilmenidine suppresses proliferation and promotes apoptosis via the mitochondrial pathway in human leukemic K562 cells

Eur J Pharm Sci. 2016 Jan 1:81:172-80. doi: 10.1016/j.ejps.2015.10.017. Epub 2015 Oct 24.

Abstract

Imidazoline I1 receptor signaling is associated with pathways that regulate cell viability leading to varied cell-type specific phenotypes. We demonstrated that the antihypertensive drug rilmenidine, a selective imidazoline I1 receptor agonist, modulates proliferation and stimulates the proapoptotic protein Bax thus inducing the perturbation of the mitochondrial pathway and apoptosis in human leukemic K562 cells. Rilmenidine acts through a mechanism which involves deactivation of Ras/MAP kinases ERK, p38 and JNK. Moreover, rilmenidine renders K562 cells, which are particularly resistant to chemotherapeutic agents, susceptible to the DNA damaging drug doxorubicin. The rilmenidine co-treatment with doxorubicin reverses G2/M arrest and triggers apoptotic response to DNA damage. Our data offer new insights into the pathways associated with imidazoline I1 receptor activation in K562 cells suggesting rilmenidine as a valuable tool to deepen our understanding of imidazoline I1 receptor signaling in hematologic malignancies and to search for medicinally active agents.

Keywords: Apoptosis; DNA damage; Imidazoline I1 receptor signaling; K562; Proliferation; Rilmenidine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibiotics, Antineoplastic / pharmacology
  • Antineoplastic Agents / pharmacology*
  • Apoptosis / drug effects
  • Caspase 3 / genetics
  • Cell Cycle / drug effects
  • Cell Proliferation / drug effects
  • Cyclin B1 / metabolism
  • Doxorubicin / pharmacology
  • Humans
  • Imidazoline Receptors / agonists*
  • Imidazoline Receptors / metabolism
  • K562 Cells
  • Leukemia / metabolism
  • Mitochondria / drug effects*
  • Mitochondria / metabolism
  • Mitogen-Activated Protein Kinases / metabolism
  • Oxazoles / pharmacology*
  • RNA, Messenger / metabolism
  • Rilmenidine
  • bcl-2-Associated X Protein / genetics

Substances

  • Antibiotics, Antineoplastic
  • Antineoplastic Agents
  • BAX protein, human
  • CCNB1 protein, human
  • Cyclin B1
  • Imidazoline Receptors
  • Oxazoles
  • RNA, Messenger
  • bcl-2-Associated X Protein
  • Doxorubicin
  • Mitogen-Activated Protein Kinases
  • Caspase 3
  • Rilmenidine