Zayas Beatriz, Lebron Vivian, Vélez Christian, Cox Osvaldo
School of Science, Technology and Environment, Ana G. Mendez University (UAGM), USA.
J Cancer Prev Curr Res. 2020;11(1):13-18. doi: 10.15406/jcpcr.2020.11.00417. Epub 2020 Jan 23.
This study presents the applicability of a novel nitro-substituted heterocyclic compound NBQ48, member of the family of compounds identified as 3 nitrobenzazolo[3, 2-a] quinolinium chloride salts (NBQS) as a screening tool to identify hypoxic tumor cells. The applicability was tested on COLO 205 colon cancer cells 2D and 3D cultures treated with NBQ48 to assess the formation of a bio-reduction fluorescent metabolite under hypoxic conditions in contrast, to those under aerobic environment. Hypoxic environment was created applying a controlled hypoxic gas chamber. Prior to testing the applicability of NBQ48 as a hypoxic fluorescent marker, cytotoxic studies where performed to identify a low-toxicity dose at 24 hours under aerobic and hypoxic environments that would allow the bio-reduction process with little toxicity. The differences in fluorescence emission after treatment was measured by fluorometer and fluorescence microscopy. Results indicated that cell treatments up to 24 hours with NBQ48 under aerobic environment did not reach an IC50 dose in COLO205 cells, however under hypoxic environment the IC50 reached at 100μM. The significant fluorescence increment after 24 and 48 hrs in 2D and 3D cultures treated with NBQ48 (75uM) at hypoxic in contrast to aerobic environments clearly demonstrated the need of a low oxygen content for the bio-reduction of the parent NBQ48. This study confirms the applicability of NBQ48 as markers for hypoxia in metabolically active 2D and 3D cultures. This hydrophilic hypoxic marker could additionally aid researchers in testing hypoxia activated pro-drugs for therapeutic applications in cancer as well as on other diseases where cellular hypoxia is a significant risk factor.
本研究介绍了一种新型硝基取代杂环化合物NBQ48的适用性,该化合物属于被鉴定为3-硝基苯并唑[3,2-a]喹啉鎓氯化物盐(NBQS)的化合物家族,可作为一种筛选工具来识别缺氧肿瘤细胞。在二维和三维培养的COLO 205结肠癌细胞上测试了NBQ48的适用性,用NBQ48处理细胞以评估缺氧条件下与有氧环境相比生物还原荧光代谢物的形成。通过使用可控缺氧气体室来营造缺氧环境。在测试NBQ48作为缺氧荧光标记物的适用性之前,进行了细胞毒性研究,以确定在有氧和缺氧环境下24小时的低毒性剂量,该剂量允许在毒性很小的情况下进行生物还原过程。通过荧光计和荧光显微镜测量处理后荧光发射的差异。结果表明,在有氧环境下用NBQ48处理COLO205细胞长达24小时未达到IC50剂量,然而在缺氧环境下IC50达到100μM。与有氧环境相比,在缺氧条件下用NBQ48(75μM)处理的二维和三维培养物在24小时和48小时后荧光显著增加,清楚地表明母体NBQ48的生物还原需要低氧含量。本研究证实了NBQ48作为代谢活跃的二维和三维培养物中缺氧标记物的适用性。这种亲水性缺氧标记物还可以帮助研究人员测试缺氧激活前药在癌症治疗中的应用以及在细胞缺氧是重要风险因素的其他疾病中的应用。