Bryostatin 1 affects P-glycoprotein phosphorylation but not function in multidrug-resistant human breast cancer cells

Clin Cancer Res. 1995 Dec;1(12):1581-7.

Abstract

The function of P-glycoprotein (Pgp), which confers multidrug resistance by active efflux of drug, is thought to be dependent on phosphorylation. Previous studies have suggested that protein kinase C (PKC) plays an important role in Pgp phosphorylation. We report here the effects of bryostatin 1, a unique PKC activator and inhibitor, on Pgp function in a multidrug-resistant MCF-7 human breast cancer subline which overexpresses PKC-alpha. Bryostatin 1 (100 nM) decreased Pgp phosphorylation after 24 h of treatment. In contrast, it did not affect Pgp function as demonstrated by the accumulation of [3H]vinblastine and rhodamine 123. We compared the effect of bryostatin 1 treatment on PKC-alpha with that of the phorbol ester 12-O-tetradecanoylphorbol-13-acetate (200 nM). 12-O-tetradecanoylphorbol-13-acetate caused translocation of PKC-alpha from the cytosol to the cell membrane after a 10-min treatment and its down-regulation after 24 h of treatment. Likewise, bryostatin 1 (100 nM) caused translocation, but only after longer treatment (1 h), and it caused down-regulation of PKC-alpha at 24 h of treatment. Thus, while the MCF-7TH cells overexpress the PKC-alpha isoform, and its down-regulation by bryostatin 1 is associated with decreased Pgp phosphorylation, these alterations do not modulate drug transport. We conclude that, while bryostatin 1 may be useful clinically because of its ability to inhibit PKC, it is not able to reverse Pgp-mediated multidrug resistance.

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / drug effects*
  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / physiology
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents / pharmacology*
  • Breast Neoplasms / metabolism*
  • Bryostatins
  • Daunorubicin / metabolism
  • Down-Regulation
  • Drug Resistance, Multiple
  • Drug Resistance, Neoplasm
  • Enzyme Activation / drug effects
  • Female
  • Humans
  • Isoenzymes / metabolism
  • Lactones / pharmacology*
  • Macrolides
  • Neoplasm Proteins / drug effects*
  • Neoplasm Proteins / physiology
  • Phosphorylation / drug effects
  • Protein Kinase C / metabolism*
  • Rhodamines / metabolism
  • Tumor Cells, Cultured / drug effects
  • Vinblastine / metabolism

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Antineoplastic Agents
  • Bryostatins
  • Isoenzymes
  • Lactones
  • Macrolides
  • Neoplasm Proteins
  • Rhodamines
  • bryostatin 1
  • Vinblastine
  • Protein Kinase C
  • Daunorubicin