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基于发光 11-(萘-1-基)二吡啶并[3,2-a:2',3'-c]吩嗪的 Ru(II)/Ir(III)/Re(I) 配合物用于 HCT-116 结直肠癌细胞治疗。

Luminescent 11-{Naphthalen-1-yl}dipyrido[3,2-a:2',3'-c]phenazine-Based Ru(II)/Ir(III)/Re(I) Complexes for HCT-116 Colorectal Cancer Stem Cell Therapy.

机构信息

Department of Chemistry, School of Advanced Sciences, Vellore Institute of Technology, Vellore 632014, Tamilnadu, India.

Department Stem Cells and Regenerative Medicine Centre, Institution Yenepoya Research Centre, Yenepoya University, University Road, Derlakatte, Mangalore 575018, Karnataka, India.

出版信息

ACS Appl Bio Mater. 2023 Feb 20;6(2):410-424. doi: 10.1021/acsabm.2c00556. Epub 2023 Jan 13.

Abstract

Due to a number of unpleasant considerations, marketed drugs have steadily lost their importance in the treatment of cancer. In order to find a viable cancer cell diagnostic agent, we therefore focused on metal complexes that displayed target adequacy, permeability to cancer cells, high standard water solubility, cytoselectivity, and luminescent behavior. In this aspect, luminescent 11-{naphthalen-1-yl} dipyrido [3,2-a:2',3'-c] phenazine based Ru(II)/Ir(III)/Re(I) complexes have been prepared for HCT-116 colorectal cancer stem cell therapy. Our study successfully established the possible cytotoxicity of complex at different doses on HCT-116 colorectal cancer stem cells (CRCSCs). Additionally, an immunochemistry analysis of the complex showed that the molecule was subcellularly localized in the nucleus and other regions of the cytoplasm, where it caused nuclear DNA damage and mitochondrial dysfunction. The level of BAX and Bcl-2 was further quantified by qRT-PCR. The expression of proapoptotic BAX showed increased expression in the complex -treated cell compared to the control, indicating the potential of complex for apoptotic induction. Upon further validation, complex was developed as an inhibitor of autophagy for the eradication of cancer stem cells.

摘要

由于一些令人不快的考虑因素,市售药物在癌症治疗中的地位稳步下降。为了找到一种可行的癌细胞诊断试剂,我们因此专注于那些具有靶标适宜性、对癌细胞的通透性、高标准的水溶性、细胞选择性和发光行为的金属配合物。在这方面,我们制备了基于 11-(萘-1-基)二吡啶并[3,2-a:2',3'-c]吩嗪的发光型 Ru(II)/Ir(III)/Re(I)配合物,用于 HCT-116 结直肠癌细胞治疗。我们的研究成功地确定了不同剂量的该配合物对 HCT-116 结直肠癌细胞(CRCSCs)的可能细胞毒性。此外,对配合物的免疫化学分析表明,该分子在细胞质的核内和其他区域定位于亚细胞内,导致核 DNA 损伤和线粒体功能障碍。通过 qRT-PCR 进一步定量了 BAX 和 Bcl-2 的水平。与对照组相比,凋亡蛋白 BAX 的表达在复合物处理的细胞中增加,表明复合物 具有诱导凋亡的潜力。经过进一步验证,该复合物被开发为自噬抑制剂,用于消除癌症干细胞。

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