Correlation Engine 2.0
Clear Search sequence regions


  • doxorubicin (5)
  • drug antitumor (1)
  • glycolysis (1)
  • Hep (1)
  • humans (1)
  • PDK (2)
  • prodrug (6)
  • Sizes of these terms reflect their relevance to your search.

    The inevitable challenge in conventional chemotherapy is to deliver the anticancer drugs to the dense population of tumors cells while minimizing the drug-associated side effects on the normal cells. Cancer cells' preference for glycolysis for energy production is well recognized. Intuitively, taking advantage of such cancer-associated metabolism would be a promising strategy for anticancer drug delivery with minimal side effects. In this investigation, we have designed a binary prodrug PDOX as a sequential drug delivery regimens to realize the combination therapy for cancer. As cancer cells exhibit abrupt metabolism with elevated pyruvate dehydrogenase kinase (PDK) activity, dichloroacetic acid (DCA, a well-known PDK inhibitor) was used in combination with anticancer drug doxorubicin (DOX). The designed molecular prodrug was activated selectively by cancer-associated esterase to deliver DCA and DOX, respectively, and induced synergetic effects. Hence, sequential targeted delivery of molecular prodrug PDOX offers a promising approach to overcome the offside drug toxicity, pharmacokinetics, and biodistribution of individuals and provide an alternative option for cancer treatment.

    Citation

    Amit Sharma, Jieun Chun, Myung Sun Ji, Sooyeon Lee, Chulhun Kang, Jong Seung Kim. Binary Prodrug of Dichloroacetic Acid and Doxorubicin with Enhanced Anticancer Activity. ACS applied bio materials. 2021 Mar 15;4(3):2026-2032

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 35014328

    View Full Text