| Literature DB >> 28371526 |
Hongmei Liu1,2, Yifan Cai1,2, Yafei Zhang1,2, Yandong Xie1,2, Hui Qiu3,4, Lei Hua1,2, Xuejiao Liu1,2, Yuling Li5, Jun Lu6, Longzhen Zhang3,4, Rutong Yu1,2.
Abstract
Gliomas are highly radioresistant tumors, mainly due to hypoxia in the core region of the gliomas and efficient DNA double-strand break repair. However, the design of a radiosensitizer incorporating the two above mechanisms is difficult and has rarely been reported. Thus, this study develops a hypoxic radiosensitizer-prodrug liposome (MLP) to deliver the DNA repair inhibitor Dbait (MLP/Dbait) to achieve the simultaneous entry of radiosensitizers with two different mechanisms into the glioma. MLP/Dbait effectively sensitizes glioma cells to X-ray radiotherapy (RT). Histological and microscopic examinations of dissected brain tissue confirm that MLP effectively delivers Dbait into the glioma. Furthermore, the combination of MLP/Dbait with RT significantly inhibits growth of the glioma, as assessed by in vivo bioluminescence imaging. These findings suggest that MLP is a promising candidate as a Dbait delivery system to enhance the effect of RT on glioma, owing to the synergistic effects of the two different radiosensitizers.Entities:
Keywords: Dbait; glioma; hypoxic radiosensitizer-prodrug; radiotherapy
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Year: 2017 PMID: 28371526 DOI: 10.1002/adhm.201601377
Source DB: PubMed Journal: Adv Healthc Mater ISSN: 2192-2640 Impact factor: 9.933