Telomerase inhibitors: a patent review (2010-2015).

Expert Opin Ther Pat

a State Key Laboratory of Pharmaceutical Biotechnology , Nanjing University, Nanjing , People's Republic of China.

Published: June 2016

AI Article Synopsis

  • Telomerase is a protein complex that adds specific DNA sequences to chromosome ends, and is highly active in most tumors but not in normal cells, making it a potential target for cancer therapy.
  • This review discusses recent advances (2010-2015) in telomerase inhibitors, including nucleoside analogues and G-quadruplex stabilizers, alongside their relationship to cancer and inflammation.
  • The article highlights the importance of developing new and more effective anti-cancer agents, particularly focusing on imetelstat (GRN163L) and G-quadruplex stabilizers as key players in telomerase inhibition.

Article Abstract

Introduction: Telomerase is a ribonucleoprotein that catalyses the addition of telomeric repeat sequences (having the sequence 5'-TTAGGG-3' in humans) to the ends of chromosomes. Telomerase activity is detected in most types of human tumours, but it is almost undetectable in normal somatic cells. Therefore, telomerase is a promising therapeutic target. To date, the known inhibitors of telomerase include nucleoside analogues, oligonucleotides and G-quadruplex stabilizers. This review highlights recent advances in our understanding of telomerase inhibitors, the relationships between telomerase inhibitors, cancer, and fields such as inflammation.

Areas Covered: This review summarizes new patents published on telomerase inhibitors from 2010 to 2015.

Expert Opinion: The review provides a brief account of the background, development, and on-going issues involving telomerase inhibitors. In particular, this review emphasizes imetelstat (GRN163L) and some typical G-quadruplex stabilizers that participate in telomerase inhibition. Overall, the research scope of antineoplastic is becoming broader and telomerase inhibitors have been shown to be a promising therapeutic target. Therefore, novel antineoplastic agents with greater activity and higher specificity must be developed.

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Source
http://dx.doi.org/10.1080/13543776.2016.1181172DOI Listing

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