| Literature DB >> 29627724 |
Liangfeng Huang1, Gaofei Wei1, Xiaoqi Sun1, Yali Jiang1, Zeqian Huang1, Yanjuan Huang1, Yifeng Shen1, Xiaoyu Xu1, Yunhui Liao1, Chunshun Zhao2.
Abstract
Therapeutic effects of photodynamic therapy (PDT) are limited by the selectivity of photosensitizer (PS). Herein, a novel tumor-targeted drug-PS conjugate (Gan-ZnPc) which integrated with zinc phthalocyanine (ZnPc) and Ganetespib has been developed. ZnPc is a promising PS with remarkable photosensitization ability. Ganetespib is a heat shock protein 90 (Hsp90) inhibitor with preferential tumor selectivity and conjugated to ZnPc as a tumor-targeted ligand. The multifunctional small molecule conjugate, Gan-ZnPc, could be bound to extracellular Hsp90 and then selectively internalized into the tumor cells, followed by the generation of abundant intracellular reactive oxygen species (ROS) upon irradiation. Besides, Gan-ZnPc can arrest cell proliferation and induce apoptosis by the inhibition of Hsp90. Herein, with combination of the inhibition of Hsp90 and the generation of cytotoxic ROS, Gan-ZnPc implements tumor selectivity, concentrated PDT and chemotherapy in a synergistic manner, which results in highly effective anti-tumor activity in vitro and in vivo.Entities:
Keywords: Chemotherapy; Heat shock protein 90; Photodynamic therapy; Tumor-targeted; Zinc phthalocyanine
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Year: 2018 PMID: 29627724 DOI: 10.1016/j.ejmech.2018.03.077
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514