Molecular avenues in targeted doxorubicin cancer therapy

Future Oncol. 2020 Apr;16(11):687-700. doi: 10.2217/fon-2019-0458. Epub 2020 Apr 7.

Abstract

In recent, intra- and inter-tumor heterogeneity is seen as one of key factors behind success and failure of chemotherapy. Incessant use of doxorubicin (DOX) drug is associated with numerous post-treatment debacles including cardiomyopathy, health disorders, reversal of tumor and formation of secondary tumors. The module of cancer treatment has undergone evolutionary changes by achieving crucial understanding on molecular, genetic, epigenetic and environmental adaptations by cancer cells. Therefore, there is a paradigm shift in cancer therapeutic by employing amalgam of peptide mimetic, small RNA mimetic, DNA repair protein inhibitors, signaling inhibitors and epigenetic modulators to achieve targeted and personalized DOX therapy. This review summarizes on recent therapeutic avenues that can potentiate DOX effects by removing discernible pitfalls among cancer patients.

Keywords: DNA damage; DNA repair; adriamycin; epigenetic; genomic instability; genotoxic; tumor.

Publication types

  • Review

MeSH terms

  • Antibiotics, Antineoplastic / adverse effects
  • Antibiotics, Antineoplastic / therapeutic use*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • DNA Repair
  • Doxorubicin / adverse effects
  • Doxorubicin / therapeutic use*
  • Drug Resistance, Neoplasm / drug effects
  • Epigenesis, Genetic
  • Humans
  • Molecular Targeted Therapy*
  • Neoplasms / drug therapy
  • Neoplasms / genetics
  • Signal Transduction

Substances

  • Antibiotics, Antineoplastic
  • Doxorubicin