| Literature DB >> 29456804 |
Shilong Zheng1,2, Shanchun Guo1,2, Qiu Zhong1,2, Changde Zhang1,2, Jiawang Liu1,2, Lin Yang2, Qiang Zhang1,2, Guangdi Wang1,2.
Abstract
Despite promising therapeutic utilities for treatment of hematological malignancies, histone deacetylase inhibitor (HDACi) drugs have not proven as effective in the treatment of solid tumors. To expand the clinical indications of HDACi drugs, we developed novel boron-containing prodrugs of belinostat (2), one of which efficiently releases active 2 through a cascade of reactions in cell culture and demonstrates activities comparable to 2 against a panel of cancer cell lines. Importantly, prodrug 7 is more efficacious than belinostat in vivo, not only inhibiting the growth of tumor but also reducing tumor volumes in an MCF-7 xenograft tumor model owing to its superior biocompatibility, which suggests its clinical potential in the treatment of solid tumors.Entities:
Year: 2018 PMID: 29456804 PMCID: PMC5807862 DOI: 10.1021/acsmedchemlett.7b00504
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345