Novel NBQ-48 as marker of hypoxic cells in 2D and 3D colon cancer cells.

Beatriz Zayas, Vivian Lebron, Christian Vélez, Osvaldo Cox
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引用次数: 1

Abstract

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.

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新型NBQ-48作为2D和3D结肠癌细胞缺氧细胞的标记物。
本研究提出了一种新的硝基取代杂环化合物NBQ48的适用性,该化合物家族的成员被鉴定为3硝基苯并唑[3,2 -a]喹啉氯化盐(NBQS)作为鉴定缺氧肿瘤细胞的筛选工具。在用NBQ48处理的COLO 205结肠癌细胞的2D和3D培养物上测试了该方法的适用性,以评估在缺氧条件下与在有氧环境下形成生物还原荧光代谢物的情况。采用可控低氧毒气室营造低氧环境。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,从而使生物还原过程毒性很小。用荧光仪和荧光显微镜测量处理后荧光发射的差异。结果表明,在好氧环境下,NBQ48处理24小时后,col205细胞的IC50剂量未达到,而在缺氧环境下,IC50达到100μM。与好氧环境相比,NBQ48 (75uM)在低氧环境下处理24小时和48小时后,2D和3D培养物的荧光显著增加,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在代谢活跃的2D和3D培养中作为缺氧标记物的适用性。这种亲水性缺氧标志物还可以帮助研究人员测试缺氧激活的前药,用于癌症和其他细胞缺氧是重要危险因素的疾病的治疗应用。
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