Punganuru Surendra Reddy, Madala Hanumantha Rao, Arutla Viswanath, Srivenugopal Kalkunte S
Department of Pharmaceutical Sciences, School of Pharmacy, Texas Tech University Health Sciences Center, Amarillo, TX 79106, USA.
Cancers (Basel). 2018 Nov 28;10(12):470. doi: 10.3390/cancers10120470.
Human NAD(P)H quinone oxidoreductase-1 (hNQO1) is an important cancer-related biomarker, which shows significant overexpression in malignant cells. Developing an effective method for detecting NQO1 activity with high sensitivity and selectivity in tumors holds a great potential for cancer diagnosis, treatment, and management. In the present study, we report a new dicyanoisophorone (DCP) based fluorescent probe (NQ-DCP) capable of monitoring hNQO1 activity in vitro and in vivo in both ratiometric and turn-on model. NQ-DCP was prepared by conjugating dicyanoisophorone fluoroprobe with hNQO1 activatable quinone propionic acid (QPA), which remain non-fluorescent until activation by tumor-specific hNQO1. NQ-DCP featured a large Stokes shift (145 nm), excellent biocompatibility, cell permeability, and selectivity towards hNQO1 allowed to differentiate cancer cells from healthy cells. We have successfully employed NQ-DCP to monitor non-invasive endogenous hNQO1 activity in brain tumor cells in vitro and in xenografted tumors developed in nude mice.
人NAD(P)H醌氧化还原酶-1(hNQO1)是一种重要的癌症相关生物标志物,在恶性细胞中显著过表达。开发一种在肿瘤中高灵敏度和高选择性检测NQO1活性的有效方法,对癌症的诊断、治疗和管理具有巨大潜力。在本研究中,我们报道了一种基于二氰基异佛尔酮(DCP)的新型荧光探针(NQ-DCP),它能够在体外和体内以比率和开启模式监测hNQO1活性。NQ-DCP是通过将二氰基异佛尔酮荧光探针与hNQO1可激活的醌丙酸(QPA)偶联制备而成,在被肿瘤特异性hNQO1激活之前一直无荧光。NQ-DCP具有大斯托克斯位移(145 nm)、优异的生物相容性、细胞渗透性以及对hNQO1的选择性,能够区分癌细胞和健康细胞。我们已成功使用NQ-DCP在体外监测脑肿瘤细胞中以及在裸鼠体内异种移植肿瘤中无创内源性hNQO1的活性。