P-glycoprotein substrates and antagonists cluster into two distinct groups

Stefania Scala, Nadia Akhmed, U. S. Rao, Ken Paull, Lu Bin Lan, Bruce Dickstein, Jong Seok Lee, Galal H. Elgemeie, Wilfred D. Stein, Susan E. Bates

Research output: Contribution to journalArticle

Abstract

To gather further insight into the interaction between P-glycoprotein (Pgp) and its substrates, 167 compounds were analyzed in multidrug resistant human colon carcinoma cells. These compounds were selected from the National Cancer institute Drug Screen repository using computer-generated correlations with known Pgp substrates and antagonists. The compounds were prospectively defined as Pgp substrates if cytotoxicity was increased ≤4-fold by the addition of cyclosporin A (CsA) and as Pgp antagonists if inhibition of efflux increased rhodamine accumulation by 4-fold. Among the 84 agents that met either criterion, 35 met only the criterion for substrates, 42 met only the criterion for antagonists, and only seven met both criteria. Thus, compounds interacting with PgP form two distinct groups: one comprising cytotoxic compounds that are transported and have poor or no antagonistic activity and a second comprising compounds with antagonistic activity and no evidence of significant transport. Vinblastine accumulation and kinetic studies performed on a subset of 18 compounds similarly differentiated substrates and antagonists, but inhibition of 3H-azidopine labeling and induction of ATPase activity did not. These data support an emerging concept of Pgp in which multiple regions instead of specific sites are involved in drug transport.

Original languageEnglish
Pages (from-to)1024-1033
Number of pages10
JournalMolecular Pharmacology
Volume51
Issue number6
Publication statusPublished - Jun 1997

ASJC Scopus subject areas

  • Pharmacology

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    Scala, S., Akhmed, N., Rao, U. S., Paull, K., Lan, L. B., Dickstein, B., Lee, J. S., Elgemeie, G. H., Stein, W. D., & Bates, S. E. (1997). P-glycoprotein substrates and antagonists cluster into two distinct groups. Molecular Pharmacology, 51(6), 1024-1033.