| Literature DB >> 29961960 |
Yang Wang1, Shenglin Luo1, Chi Zhang1, Xingyun Liao1, Tao Liu1, Zhongyong Jiang1, Dengqun Liu1, Xu Tan1, Lei Long1, Yu Wang1, Zelin Chen1, Yunsheng Liu1, Fan Yang1, Yibo Gan1, Chunmeng Shi1.
Abstract
The endoplasmic reticulum (ER) stress signaling or unfolded protein response (UPR) is a common feature of many human diseases, including cancer. Excessive activation of ER stress directly induces cell death, holding a new promising strategy for the therapeutic intervention of cancer. Current ER-stress-inducing agents mainly target UPR components or proteasomes, which exert limited treatment efficacy and undesired side effects due to unselective ER stress and poor tumor-specific distribution. In this study, a unique near-infrared (NIR) fluorophore, IR-34, is synthesized and identified to selectively and efficiently trigger tumoricidal ER stress by targeting the mitochondrial protein NDUFS1. IR-34 is demonstrated to specifically accumulate in living cancer cells for tumor NIR imaging and drastically inhibit tumor growth and recurrence without causing apparent toxicity. Thus, this multifunctional NIR fluorophore may represent a novel theranostic agent for tumor imaging-guided treatment and also strengthens the idea that mitochondria could be a useful target for therapeutic ER stress in cancer cells.Entities:
Keywords: ER stress; NDUFS1; NIR fluorphores; mitochondrial complexes I
Year: 2018 PMID: 29961960 DOI: 10.1002/adma.201800475
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849