P-glycoprotein expression in bladder cancer

J Urol. 1994 Jan;151(1):43-6. doi: 10.1016/s0022-5347(17)34868-1.

Abstract

Multi-drug resistance is a phenomenon by which tumor cells express resistance to a variety of chemically unrelated chemotherapeutic drugs. The classical form of multi-drug resistance is mediated through the expression of P-glycoprotein, which acts as an energy dependent drug efflux pump. P-glycoprotein expression was evaluated in 29 cystectomy specimens from patients with bladder cancer with no prior exposure to chemotherapeutic drugs, and in bladder biopsies from 9 subjects before treatment with intravesical doxorubicin. Furthermore, the strategy of circumvention of P-glycoprotein-mediated resistance using the combination of doxorubicin and verapamil intravesically was tested in 5 patients. P-glycoprotein was expressed in 75% of the cystectomy specimens. In the doxorubicin treated patients no correlation was noted between P-glycoprotein expression on the initial tumors and subsequent response to doxorubicin. The pilot trial of verapamil and doxorubicin was well tolerated but did not suggest increased efficacy of this combination. P-glycoprotein can be expressed on bladder cancer cells without prior chemotherapy. The role of P-glycoprotein mediated multi-drug resistance in bladder cancer treatment failure remains to be defined.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Administration, Intravesical
  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Carrier Proteins / analysis
  • Carrier Proteins / biosynthesis*
  • Carrier Proteins / drug effects
  • Doxorubicin / administration & dosage
  • Doxorubicin / pharmacology*
  • Doxorubicin / therapeutic use
  • Drug Resistance*
  • Female
  • Follow-Up Studies
  • Humans
  • Male
  • Membrane Glycoproteins / analysis
  • Membrane Glycoproteins / biosynthesis*
  • Membrane Glycoproteins / drug effects
  • Middle Aged
  • Neoplasm Recurrence, Local / prevention & control
  • Pilot Projects
  • Urinary Bladder Neoplasms / chemistry
  • Urinary Bladder Neoplasms / drug therapy
  • Urinary Bladder Neoplasms / metabolism*
  • Urinary Bladder Neoplasms / prevention & control
  • Verapamil / administration & dosage
  • Verapamil / pharmacology*
  • Verapamil / therapeutic use

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Carrier Proteins
  • Membrane Glycoproteins
  • Doxorubicin
  • Verapamil