Regorafenib is transported by the organic anion transporter 1B1 and the multidrug resistance protein 2

Hiroki Ohya, Yoshihiko Shibayama, Jiro Ogura, Katsuya Narumi, Masaki Kobayashi, Ken Iseki

Research output: Contribution to journalArticlepeer-review

20 Citations (Scopus)

Abstract

Regorafenib is a small molecule inhibitor of tyrosine kinases, and has been shown to improve the outcomes of patients with advanced colorectal cancer and advanced gastrointestinal stromal tumors. The transport profiles of regorafenib by various transporters were evaluated. HEK293/organic anion transporting polypeptide 1B1 (OATP1B1) cells exhibited increased drug sensitivity to regorafenib. Regorafenib inhibited the uptake of 3H-estrone sulfate by HEK293/OATP1B1 cells in a dose-dependent manner, but did not affect its elimination by P-glycoproteins. The concentration of regorafenib was significantly lower in LLC-PK1/multidrug resistance protein 2 (MRP2) cells than in LLC-PK1 cells treated with the MRP2 inhibitor, MK571. MK571 abolished the inhibitory effects of regorafenib on intracellular accumulation in LLC-PK1/MRP2 cells. The uptake of regorafenib was significantly higher in HEK293/OATP1B1 cells than in OATP1B1-mock cells. Transport kinetics values were estimated to be Km = 15.9 μM and Vmax = 1.24 nmol/mg/min. No significant difference was observed in regorafenib concentrations between HEK293/OATP1B3 and OATP1B3-mock cells. These results indicated that regorafenib is a substrate for MRP2 and OATP1B1, and also suggest that the substrate preference of regorafenib may implicate the pharmacokinetic profiles of regorafenib.

Original languageEnglish
Pages (from-to)582-586
Number of pages5
JournalBiological and Pharmaceutical Bulletin
Volume38
Issue number4
DOIs
Publication statusPublished - 2015 Apr 1
Externally publishedYes

Keywords

  • IC
  • Multidrug resistance protein 2
  • Organic anion transporting polypeptide 1B1
  • Regorafenib
  • Vectorial drug transport

ASJC Scopus subject areas

  • Pharmacology
  • Pharmaceutical Science

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