Published April 28, 2016 | Version Published
Book Section - Chapter Open

Chapter 8. Polymeric Nanoparticles and Cancer: Lessons Learnt from CRLX101

  • 1. ROR icon Taipei Medical University
  • 2. ROR icon Cerulean Pharma (United States)
  • 3. ROR icon California Institute of Technology
  • 4. ROR icon City Of Hope National Medical Center

Contributors

Abstract

CRLX101 (formerly IT-101) is a novel cyclodextrin-based polymer that self-assembles into nanoparticles. CRLX101 is covalently conjugated to the hydrophobic topoisomerase 1 (TOP1)-inhibitor camptothecin (CPT) resulting in stabilized structure and increased water solubility. Extensive preclinical studies of CRLX101 demonstrated delayed renal clearance and a prolonged plasma half-life. The nanoparticle passively accumulates in tumour tissue through the enhanced permeability and retention effect and slowly releases active CPT leading to enhanced TOP1 inhibition, potential hypoxia inducible factor-1α (HIF-1α) effect, cancer stem cell targeting, and increased antitumour activity against multiple human tumour xenografts. More than 200 human cancer patients have been treated with CRLX101 in phase I/IIa and phase II clinical trials. In this chapter we explore a wide range of anti-cancer nanotherapeutic strategies to inhibit TOP1, HIF-1α and cancer stem cells. Moreover, we discuss the therapeutic value of combining HIF-1α inhibition with antiangiogenics. Finally, we return to CRLX101 and cover in detail the latest preclinical and clinical evaluations and discuss future directions.

Additional Information

© 2016 Royal Society of Chemistry.

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Identifiers

Eprint ID
69313
Resolver ID
CaltechAUTHORS:20160729-120515808

Dates

Created
2016-07-29
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Updated
2021-11-11
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Caltech Custom Metadata

Series Name
RSC Drug Discovery Series
Series Volume or Issue Number
51