Irinotecan and temozolomide brain distribution: a focus on ABCB1

Cancer Chemother Pharmacol. 2014 Jul;74(1):185-93. doi: 10.1007/s00280-014-2490-0. Epub 2014 May 28.

Abstract

Glioblastoma (GBM), the most common primary brain tumor in adults, is usually rapidly fatal with median survival duration of only 15 months and a 3-year survival rate of <7 %. Temozolomide (TMZ) is the only anticancer drug that has improved survival in GBM when administered with concomitant radiotherapy. Irinotecan (CPT-11) has also shown efficacy in recurrent gliomas monotherapy with moderate response. As the efficacy of GBM treatments relies on their brain distribution through the blood-brain barrier (BBB), the aim of the present work was to study, on an in vivo model, the brain distribution of TMZ, CPT-11 and its active metabolite, SN-38. We have focussed on the role of ABCB1, the main efflux transporter at the BBB level, through pharmacokinetics studies in CF1 mdr1a(+/+) and mdr1a(-/-) mice. Our results show that TMZ, CPT-11 and SN-38 are transported by ABCB1 at the BBB level with brain/plasma ratios of 1.1, 2.1 and 2.3, respectively.

Publication types

  • Comparative Study

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B / genetics
  • ATP Binding Cassette Transporter, Subfamily B / metabolism*
  • Animals
  • Antineoplastic Agents, Alkylating / administration & dosage
  • Antineoplastic Agents, Alkylating / blood
  • Antineoplastic Agents, Alkylating / metabolism
  • Antineoplastic Agents, Alkylating / pharmacokinetics*
  • Antineoplastic Agents, Phytogenic / administration & dosage
  • Antineoplastic Agents, Phytogenic / blood
  • Antineoplastic Agents, Phytogenic / metabolism
  • Antineoplastic Agents, Phytogenic / pharmacokinetics
  • Biological Transport / drug effects
  • Blood-Brain Barrier / drug effects
  • Blood-Brain Barrier / metabolism*
  • Brain / drug effects
  • Brain / metabolism*
  • Camptothecin / administration & dosage
  • Camptothecin / analogs & derivatives*
  • Camptothecin / blood
  • Camptothecin / metabolism
  • Camptothecin / pharmacokinetics
  • Dacarbazine / administration & dosage
  • Dacarbazine / analogs & derivatives*
  • Dacarbazine / blood
  • Dacarbazine / metabolism
  • Dacarbazine / pharmacokinetics
  • Female
  • Half-Life
  • Injections, Intraperitoneal
  • Irinotecan
  • Mice
  • Mice, Inbred Strains
  • Mice, Mutant Strains
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Neurons / drug effects
  • Neurons / metabolism
  • Prodrugs / administration & dosage
  • Prodrugs / metabolism
  • Prodrugs / pharmacokinetics
  • Temozolomide
  • Tissue Distribution
  • Topoisomerase I Inhibitors / administration & dosage
  • Topoisomerase I Inhibitors / blood
  • Topoisomerase I Inhibitors / metabolism
  • Topoisomerase I Inhibitors / pharmacokinetics*

Substances

  • ATP Binding Cassette Transporter, Subfamily B
  • Antineoplastic Agents, Alkylating
  • Antineoplastic Agents, Phytogenic
  • Nerve Tissue Proteins
  • Prodrugs
  • Topoisomerase I Inhibitors
  • Irinotecan
  • Dacarbazine
  • multidrug resistance protein 3
  • Camptothecin
  • Temozolomide