Lee Jaehun, Lee Hwunjae, Kim Hyun Jung, Yun Jongsu, Lee Taeha, Lee Gyudo, Kim Hyun Soo, Hong Yoochan
Department of Medical Device, Korea Institute of Machinery and Materials (KIMM), Daegu, 42994, Republic of Korea.
Department of Radiology, College of Medicine, Yonsei University, Seoul, 03722, Republic of Korea.
Mater Today Bio. 2022 Mar 12;14:100241. doi: 10.1016/j.mtbio.2022.100241. eCollection 2022 Mar.
Redox activity is known to regulate migration, invasion, metastasis, proliferation, and vascularization of cancer. Because cancer is heterogeneous, the role of redox activity in different cancers and cancer-related processes vary widely. In this study, water soluble, Tween 80-coated polyaniline (TPAni) nanoparticles were synthesized and used as nano-agents for sensing the redox activities of various cancer cells. To identify the relationship between the redox activity and the aggressiveness of cancer cells, two different cancer cell lines, derived from the same tissue but different with regards to aggressiveness, were selected for study. First, the cancer cell lines were incubated with TPAni nanoparticles, and an absorbance ratio obtained from the cell culture media was used as a colorimetric indicator of the redox activities of the cells. Simultaneously, hydrophobically modified filter papers coated with silver nanosnowflakes (SNSF) were used as sensing substrates for surface enhanced Raman scattering (SERS). SERS spectra obtained from varying concentrations of rhodamine 6G were used to confirm the detection limit of the SNSF-based SERS substrate. Cell culture media containing TPAni nanoparticles were treated with the SNSF-containing SERS substrates to examine the redox activities of the various cancer cell lines.The redox activities of cancer cell lines were confirmed by absorbance spectral analysis, and these redox activities were better identified via an SERS analysis method. A SNSF-containing SERS substrate, fabricated from SNSF and filter paper, was used to sense redox activity in cancer cell lines and to further identify correlations between redox activity and cancer cell line aggressiveness, as indicated by the use of EpCAM as a biomarker. Finally, potential of redox activity sensing was also confirmed.
已知氧化还原活性可调节癌症的迁移、侵袭、转移、增殖和血管生成。由于癌症具有异质性,氧化还原活性在不同癌症及癌症相关过程中的作用差异很大。在本研究中,合成了水溶性、吐温80包覆的聚苯胺(TPAni)纳米颗粒,并将其用作检测各种癌细胞氧化还原活性的纳米试剂。为了确定氧化还原活性与癌细胞侵袭性之间的关系,选择了源自同一组织但侵袭性不同的两种不同癌细胞系进行研究。首先,将癌细胞系与TPAni纳米颗粒孵育,从细胞培养基中获得的吸光度比值用作细胞氧化还原活性的比色指标。同时,将涂有银纳米雪花(SNSF)的疏水改性滤纸用作表面增强拉曼散射(SERS)的传感基底。从不同浓度的罗丹明6G获得的SERS光谱用于确认基于SNSF的SERS基底的检测限。用含SNSF的SERS基底处理含有TPAni纳米颗粒的细胞培养基,以检测各种癌细胞系的氧化还原活性。通过吸光光谱分析确认癌细胞系的氧化还原活性,并且通过SERS分析方法能更好地识别这些氧化还原活性。由SNSF和滤纸制成的含SNSF的SERS基底用于检测癌细胞系中的氧化还原活性,并进一步确定氧化还原活性与癌细胞系侵袭性之间的相关性,以上皮细胞黏附分子(EpCAM)作为生物标志物来表示。最后,还证实了氧化还原活性传感的潜力。