In vivo anti-tumor activity of a new doxorubicin conjugate via α-linolenic acid

Biosci Biotechnol Biochem. 2012;76(8):1577-9. doi: 10.1271/bbb.120256. Epub 2012 Aug 7.

Abstract

The conventional chemotherapy agent, doxorubicin, is of limited clinical use because of its systemic toxicity toward normal healthy tissue. A new doxorubicin conjugate with α-linolenic acid showed good anti-tumor activity with lower toxicity than free doxorubicin and exhibited an active tumor-targeting profile due to the introduction of α-linolenic acid which might be an effective tumor-targeting moiety for the modification of chemotherapeutics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / pharmacology*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / mortality
  • Breast Neoplasms / pathology
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Dose-Response Relationship, Drug
  • Doxorubicin / analogs & derivatives*
  • Doxorubicin / chemical synthesis
  • Doxorubicin / pharmacology*
  • Endocytosis / drug effects
  • Female
  • Humans
  • Inhibitory Concentration 50
  • Mice
  • Mice, SCID
  • Molecular Targeted Therapy
  • Neoplasm Transplantation
  • Survival Rate
  • Tumor Burden / drug effects
  • Xenograft Model Antitumor Assays
  • alpha-Linolenic Acid / chemistry*

Substances

  • Antineoplastic Agents
  • alpha-Linolenic Acid
  • Doxorubicin