o-(β-Hydroxyethyl)-rutoside-mediated Protection of Renal Injury Associated with cis-Diamminedichloroplatinum(II)/Hyperthermia Treatment

Joan M. Bull, Frederick R. Strebel, Brent A. Sunderland, Ruth Ellen Bulger, Michael Edwards, Zahid H. Siddik, Robert A. Newman

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Abstract

A bioflavonoid, o-(β-hydroxyethyl)-rutoside, has been investigated for its potential to increase the therapeutic index of the combined treatment modalities of whole body hypothermia (WBH) (41.5°C) and chemotherapy (cisplatin) in studies utilizing a transplantable fibrosarcoma solid tumor model in Fischer rats. When whole body WBH was induced 45 min after cisplatin administration, a significantly increased tumor growth delay was noted beyond that achieved by either treatment modality alone. The combination of WBH and cisplatin treatments, however, produced an unacceptable increase in renal injury. o-(β-Hydroxyethyl)-rutotoside administration was found to effectively block the renal injury without interfering with the antitumor efficacy of the combined regimen. Potential explanations for the ability of o-(β-hydroxyethyl)-rutoside to affect the increase in WBH-cisplatin therapeutic regimen are discussed.

Original languageEnglish (US)
Pages (from-to)2239-2244
Number of pages6
JournalCancer Research
Volume48
Issue number8
StatePublished - 1988

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

Fingerprint

Dive into the research topics of 'o-(β-Hydroxyethyl)-rutoside-mediated Protection of Renal Injury Associated with cis-Diamminedichloroplatinum(II)/Hyperthermia Treatment'. Together they form a unique fingerprint.

Cite this