| Literature DB >> 28580971 |
Yan-Hua Zhu1, Chun-Yang Sun1, Song Shen1, Malik I U Khan1, Yang-Yang Zhao1, Yang Liu1, Yu-Cai Wang1, Jun Wang1.
Abstract
Platinum-based chemotherapy as first-line treatment for lung cancers encounters insufficient selectivity, severe side effects and drug resistance in clinics. In this study, we developed an amphiphilic prodrug of cisplatin-poly(ethylene glycol)-block-polycaprolactone and demonstrated that the prodrug formed micellar nanoparticles, NPPt(IV), with an average diameter of ∼100 nm. NPPt(IV) released platinum in response to the intracellular acidic and reductive environment, and in turn induced significant anti-proliferative activity in lung cancer cells. More importantly, NPPt(IV) exhibited a prominent inhibitory effect on CD133+ lung cancer stem cells (CSCs) and suppressed tumor growth in vivo. Unlike cisplatin treatment which eventually enriches CSCs, NPPt(IV) treatment prevents the accumulation of CD133+ lung CSCs in tumors. Therefore, NPPt(IV) simutaneously targeting CSCs and non-CSCs might represent a superior strategy to improve conventional anticancer therapy directed predominantly to tumor bulk populations.Entities:
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Year: 2017 PMID: 28580971 DOI: 10.1039/c7bm00278e
Source DB: PubMed Journal: Biomater Sci ISSN: 2047-4830 Impact factor: 6.843