Department of Food Biotechnology, Division of Bioindustry, Silla University, Busan 46958, Korea.
Department of Cogno-Mechatronics Engineeering, College of Nanoscience & Nanotechnology, Pusan National University, Busan 46241, Korea.
Nutrients. 2018 Dec 21;11(1):20. doi: 10.3390/nu11010020.
is a commonly used medicinal mushroom containing various therapeutic effects such as anti-inflammatory, anti-allergic, and anti-cancer activities. This study examined whether on germinated soybeans (GSC) has a suppressive effect on a v-ki-ras2 Kirsten rat sarcoma viral oncogene homolog (KRAS)-driven colorectal cancer which is notorious for its un-druggable features and the ineffectiveness of conventional therapies against it. GSC extract was prepared and its proximate composition and amino acids were analyzed. The suppressive effects were investigated with the KRAS-driven colorectal cancer cell-line, SW480. SW480 proliferation, clonogenic potential, apoptosis, and the RAS/extracellular signal-regulated kinase (ERK) pathway under the GSC treatment were analyzed by 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium (MTS) assay, flow cytometry, and Western blot, respectively. An experiment with the SW480 xenograft mouse model was performed. As a result, GSC suppressed cell proliferation by inducing the apoptosis of KRAS-driven colorectal cancer cells and inhibited clonogenic capabilities. The decrease of KRAS and ERK phosphorylation was detected by Western blot. Tumor growth was significantly suppressed when GSC was introduced to the tumor-xenograft mouse model. In conclusion, GSC suppressed KRAS-driven colorectal cancer growth both in vitro and in vivo, and can be used as an alternative or simultaneous approach in colorectal cancer therapy.
灵芝是一种常用的药用蘑菇,具有抗炎、抗过敏和抗癌等多种治疗作用。本研究探讨了发芽大豆(GSC)对 KRAS 驱动的结直肠癌细胞是否具有抑制作用,KRAS 驱动的结直肠癌细胞以其不可成药的特征和传统疗法对其无效而臭名昭著。制备 GSC 提取物并分析其近似组成和氨基酸。通过 3-(4,5-二甲基噻唑-2-基)-5-(3-羧基甲氧基苯基)-2-(4-磺苯基)-2H-四唑(MTS)测定法、流式细胞术和 Western blot 分别分析了 KRAS 驱动的结直肠癌细胞系 SW480 中的 GSC 处理的抑制作用。进行了 SW480 异种移植小鼠模型实验。结果表明,GSC 通过诱导 KRAS 驱动的结直肠癌细胞凋亡来抑制细胞增殖,并抑制集落形成能力。Western blot 检测到 KRAS 和 ERK 磷酸化减少。当将 GSC 引入肿瘤异种移植小鼠模型时,肿瘤生长明显受到抑制。总之,GSC 抑制了 KRAS 驱动的结直肠癌细胞在体外和体内的生长,可作为结直肠癌治疗的替代或联合方法。