Han Ji-Su, Boo Hye-Jin, Hyun Jin Won, Song Heesang, Chang In-Youb, Yoon Sang-Pil
Jeju Research Center for Natural Medicine, Jeju National University, Jeju, 63243, Republic of Korea.
Department of Biochemistry and Molecular Biology, Chosun University School of Medicine, Gwangju, 61452, Republic of Korea.
Oncol Res. 2025 Mar 19;33(4):873-884. doi: 10.32604/or.2024.052003. eCollection 2025.
Chitosan oligosaccharide (COS) is the major degradation product of chitosan by enzymatic processes. COS, with complete water solubility, exerts significant biological effects, including anti-cancer activity. We investigated the anti-tumor effects of COS on colorectal cancer as effective therapeutic methods with low side effects are lacking.
COS was obtained from low molecular weight chitosan by an enzymatic method and the anti-cancer effects were measured by cell viability assay, flow cytometry analysis, Western blotting, and xenograft.
COS suppressed the proliferation of SNU-C5 cells compared to other colorectal cancer cells, but higher concentrations were required in the xenograft model. Co-treatment with 5-fluorouracil (5-FU) and COS enhanced the anti-cancer effects of 5-FU in SNU-C5 cells and . Flow cytometry revealed that COS induced cell cycle arrest at the G0/G1 phase without 5-FU or at the S and G2/M phases with 5-FU but did not affect cell death pathways. COS increased extracellular signal-regulated protein kinase (ERK) activation with or without 5-FU, whereas 5-FU treatment increased p53 activation. A low-dose of an ERK inhibitor suppressed COS-induced ERK activation and resulted in higher proliferation compared with COS.
These results suggest that COS might enhance the anti-cancer effects of 5-FU in SNU-C5 colorectal cancer cells by activating ERK.
壳寡糖(COS)是壳聚糖经酶促降解产生的主要产物。COS具有完全水溶性,具有显著的生物学效应,包括抗癌活性。由于缺乏低副作用的有效治疗方法,我们研究了COS对结直肠癌的抗肿瘤作用。
通过酶法从低分子量壳聚糖中获得COS,并通过细胞活力测定、流式细胞术分析、蛋白质印迹法和异种移植实验来检测其抗癌效果。
与其他结直肠癌细胞相比,COS抑制了SNU-C5细胞的增殖,但在异种移植模型中需要更高的浓度。5-氟尿嘧啶(5-FU)与COS联合处理增强了5-FU对SNU-C5细胞的抗癌作用。流式细胞术显示,COS在无5-FU时诱导细胞周期停滞在G0/G1期,在有5-FU时诱导细胞周期停滞在S期和G2/M期,但不影响细胞死亡途径。无论有无5-FU,COS均可增加细胞外信号调节蛋白激酶(ERK)的激活,而5-FU处理可增加p53的激活。低剂量的ERK抑制剂抑制了COS诱导的ERK激活,与COS相比导致更高的细胞增殖。
这些结果表明,COS可能通过激活ERK增强5-FU对SNU-C5结直肠癌细胞的抗癌作用。