Journal of Clinical and Translational Science (Mar 2021)

55484 Dual activation of CAR and Nrf2 improves the efficacy: toxicity ratio of cyclophosphamide and doxorubicin-based treatment of TNBC

  • Sydney Stern,
  • Dongdong Liang,
  • Linhao Li,
  • Ritika Kurian,
  • Caitlin Lynch,
  • Scott Heyward,
  • Ajoke Kareem,
  • Young Chun,
  • Charles Hong,
  • Fengtian Xue,
  • Hongbing Wang

DOI
https://doi.org/10.1017/cts.2021.653
Journal volume & issue
Vol. 5
pp. 98 – 98

Abstract

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ABSTRACT IMPACT: Triple negative breast cancer (TNBC) affects 10-20% of women with breast cancer and is biologically more aggressive than other subtypes. The novel compound we have developed, DL7076, would give clinicians a vital strategy to improve the commonly used cyclophosphamide (CPA) and doxorubicin (DOX) regimen in the treatment of TNBC. OBJECTIVES/GOALS: The objective of this research project is to develop a novel compound which can activate both 1) the constitutive androstane receptor (CAR) and subsequently enhance the CYP2B6-mediated activation of CPA, and 2) the nuclear factor erythroid- related factor-2 (Nrf2) leading to the cardiomyocyte protection from DOX-associated cardiotoxicity. METHODS/STUDY POPULATION: Following the identification of the compound candidate, DL7076 was evaluated for tissue specific induction of CAR and Nrf2 using qPCR, western blot analysis, and luciferase reporter assays.