| Literature DB >> 29207873 |
Guo-Bin Ding1,2, Junqing Sun1,2, Peng Yang1,2, Binchun Li1, Ying Gao3, Zhuoyu Li1,2,3.
Abstract
Glucose-regulated protein of 78 kDa (GRP78) has become an attractive and novel target for tumor therapy. Design and construction of powerful delivery systems that could efficiently transport doxorubicin (DOX) to a tumor-cell nucleus remains a formidable challenge for improving the tumor therapeutic index and mitigating side effects to normal tissues. Herein, a novel doxorubicin prodrug (NDP) with GRP78 recognition and nucleus-targeting ability was synthesized by a facile chemical route. NDP exhibited an enhanced antiproliferative activity against colorectal cancer cells and could efficiently enter the cell nucleus. Furthermore, it is inspiring to note that NDP displayed a much stronger inhibitory efficacy against the growth of colorectal cancer xenografts in nude mice than free DOX and showed superior in vivo safety. Together, the work provides a novel GRP78 and nucleus-targeting strategy, and the NDP holds great promise to be used as a potent and safe chemotherapeutic agent.Entities:
Keywords: GRP78; antitumor efficacy; bifunctional peptide; novel doxorubicin prodrug; nucleus targeting
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Year: 2017 PMID: 29207873 DOI: 10.1021/acs.molpharmaceut.7b00830
Source DB: PubMed Journal: Mol Pharm ISSN: 1543-8384 Impact factor: 4.939