Research Institute of Life Science, College of Veterinary Medicine, Gyeongsang National University, Jinju, Gyeongsang 52828, Republic of Korea.
Department of Internal Medicine, Institute of Health Sciences, Gyeongsang National University School of Medicine, Jinju, Gyeongsang 52727, Republic of Korea.
Mol Med Rep. 2017 Oct;16(4):5386-5392. doi: 10.3892/mmr.2017.7232. Epub 2017 Aug 11.
Protein array technology not only identifies a large number of proteins but also determines their expression levels. In the present study, antibody array analysis is used to decipher the proteins involved in hesperidin-induced cell death in HepG2 cells. Altered proteins in hesperidin treated cells were compared with that of untreated control cells by using a RayBio® Label‑based (L series) human antibody array kit. The identified proteins were further confirmed using western blot analysis. STRING software based analysis was used to determine the protein‑protein interactions. Many proteins related to signal transduction, cellular mechanisms, cell growth and proliferation regulatory proteins were identified. Among the proteins identified Hsp90, Smac/DIABLO, Prdx6 and FRK were significantly reduced in hesperidin treated cells. To the best of the authors' knowledge, the present study is the first to use antibody array for identifying proteins marker in hesperidin‑induced cell death in HepG2 cells. The present study provides a novel insight into the anticancer mechanism of hesperidin.
蛋白质芯片技术不仅可以鉴定大量的蛋白质,还可以确定它们的表达水平。在本研究中,抗体芯片分析用于破译橙皮苷诱导 HepG2 细胞死亡过程中涉及的蛋白质。通过使用 RayBio® Label-based(L 系列)人类抗体芯片试剂盒,将橙皮苷处理细胞中的改变蛋白与未经处理的对照细胞进行比较。使用 Western blot 分析进一步确认鉴定出的蛋白质。使用基于 STRING 软件的分析来确定蛋白质-蛋白质相互作用。确定了许多与信号转导、细胞机制、细胞生长和增殖调节蛋白相关的蛋白质。在鉴定出的蛋白质中,Hsp90、Smac/DIABLO、Prdx6 和 FRK 在橙皮苷处理的细胞中明显减少。据作者所知,本研究首次使用抗体芯片鉴定橙皮苷诱导的 HepG2 细胞死亡中的蛋白质标志物。本研究为橙皮苷的抗癌机制提供了新的见解。