Department of Nanobiotechnology, Tarbiat Modares University, P.O. Box 14115-175, Tehran, Iran.
Department of Nanobiotechnology, Tarbiat Modares University, P.O. Box 14115-175, Tehran, Iran.
Talanta. 2018 Aug 15;186:44-52. doi: 10.1016/j.talanta.2018.04.009. Epub 2018 Apr 4.
Nowadays, cancer is one of the most dangerous and deadly disease all around the world. Cancer that is diagnosed at early stages is more likely to be treated successfully. Treatment of progressed cancer is very difficult, and generally surviving rates are much lower. Therefore, much research has been focused on developing non-invasive methods for detection of cancer and monitoring of its progress. Within this contribution, we present a novel strategy for selective isolation and detection of breast cancer cell lines (MCF-7 and BT-20) based on surface enhanced Raman scattering (SERS). A simplified protocol based on cell-aptamer interaction has been developed in which core-shell (Au@FeO) nanoparticles (CSNs) were functionalized with a mucin 1 (MUC1) specific aptamer (Apt1) to capture cells through the interaction between Apt1 and overexpressed protein (MUC1) on the surface of the tumor cells. Meanwhile, a SERS nano-tag, synthesized by the conjugation of Apt1 to the surface of BSA coated and with 4-mercaptopyridine (4-Mpy) functionalized gold nanoparticles, was used to detect the isolated cells. As a conclusion, the proposed strategy can be extended to isolate and detect cells more precisely based on the detection of different kinds of biomarkers on the surface of cancer cells, simultaneously.
如今,癌症是全世界最危险和致命的疾病之一。在早期诊断出的癌症更有可能成功治疗。晚期癌症的治疗非常困难,一般存活率要低得多。因此,许多研究都集中在开发用于癌症检测和进展监测的非侵入性方法上。在本研究中,我们提出了一种基于表面增强拉曼散射(SERS)的用于选择性分离和检测乳腺癌细胞系(MCF-7 和 BT-20)的新策略。我们开发了一种简化的基于细胞-适体相互作用的方案,其中核壳(Au@FeO)纳米粒子(CSNs)通过与肿瘤细胞表面过度表达的蛋白(MUC1)之间的相互作用,用粘蛋白 1(MUC1)特异性适体(Apt1)功能化,以捕获细胞。同时,通过将 Apt1 与 BSA 涂层表面偶联,并与 4-巯基吡啶(4-Mpy)功能化的金纳米粒子结合,合成了一种 SERS 纳米标记物,用于检测分离的细胞。总之,该策略可以扩展到基于癌细胞表面不同类型生物标志物的检测,更精确地分离和检测细胞。