TY - CHAP
T1 - Polymeric nanoparticles and cancer
T2 - Lessons learnt from CRLX101
AU - Gritli, Ismael
AU - Garmey, Edward
AU - Eliasof, Scott
AU - Tellez, Andres
AU - Davis, Mark E.
AU - Yun, Yen
PY - 2016
Y1 - 2016
N2 - 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-1a (HIF-1a) 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-1a and cancer stem cells. Moreover, we discuss the therapeutic value of combining HIF-1a inhibition with antiangiogenics. Finally, we return to CRLX101 and cover in detail the latest preclinical and clinical evaluations and discuss future directions.
AB - 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-1a (HIF-1a) 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-1a and cancer stem cells. Moreover, we discuss the therapeutic value of combining HIF-1a inhibition with antiangiogenics. Finally, we return to CRLX101 and cover in detail the latest preclinical and clinical evaluations and discuss future directions.
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U2 - 10.1039/9781782622536-00199
DO - 10.1039/9781782622536-00199
M3 - Chapter
AN - SCOPUS:84974846082
VL - 2016-January
T3 - RSC Drug Discovery Series
SP - 199
EP - 232
BT - Privileged Scaffolds in Medicinal Chemistry: Design, Synthesis, Evaluation
PB - Royal Society of Chemistry
ER -