Kheyrandish Setare, Rastgar Amirhossein, Hamidi Masoud, Sajjadi Seyed Mehdi, Sarab Gholamreza Anani
Student Research Committee, Birjand University of Medical Sciences, Birjand, Iran.
Department of Medical Biotechnology, Faculty of Paramedicine, Guilan University of Medical Sciences, Rasht, Iran; BioMatter-Biomass Transformation Lab (BTL), École Polytechnique de Bruxelles, Université Libre de Bruxelles, Avenue F.D. Roosevelt, 50-CP 165/61, 1050 Brussels, Belgium.
Int J Biol Macromol. 2022 May 1;206:21-28. doi: 10.1016/j.ijbiomac.2022.02.113. Epub 2022 Feb 23.
Recently, the development and application of fungal exopolysaccharides (EPS) as natural biopolymers are on the rise. The present study is based on the investigation of possible antiproliferative and antioxidant activities of EPS from the Rhodotorula mucilaginosa sp. GUMS16 on BCR-ABL positive cells (K562). The cytotoxicity, colony formation assays lactate and dehydrogenase (LDH) activity were performed to assess the possible cancer cell death. To elucidate the underlying antiproliferative mechanism of the EPS, cell cycle analysis following real-time PCR (gene expression assessment) were evaluated. The results indicated that, the EPS with an IC50 dose of 1500 μg/ml, reduced the viability of K562 cells without having toxic effects on normal cells as well as decrease in size and number of colonies in EPS-treated group (p < 0.0001). The increase of LDH was 2.75 times more than the control (p < 0.0001). Gene expression revealed up- and down-regulation of apoptotic and anti-apoptotic genes in EPS group compared with the control. Moreover, the DPPH scavenging activity of the EPS in treated cells was significantly higher than the control group (p < 0.0001). Taken together, we concluded that the EPS from GUMS16 strain is able to inhibit the growth of K562 cells besides having antioxidant activities.
最近,作为天然生物聚合物的真菌胞外多糖(EPS)的开发与应用正在兴起。本研究基于对粘红酵母GUMS16菌株的EPS对BCR-ABL阳性细胞(K562)可能具有的抗增殖和抗氧化活性的研究。进行了细胞毒性、集落形成试验、乳酸和脱氢酶(LDH)活性测定以评估可能的癌细胞死亡情况。为阐明EPS潜在的抗增殖机制,对实时PCR后的细胞周期分析(基因表达评估)进行了评估。结果表明,IC50剂量为1500μg/ml的EPS降低了K562细胞的活力,对正常细胞无毒性作用,且在EPS处理组中菌落大小和数量减少(p<0.0001)。LDH的增加比对照组高2.75倍(p<0.0001)。基因表达显示,与对照组相比,EPS组中凋亡和抗凋亡基因有上调和下调。此外,处理细胞中EPS的DPPH清除活性显著高于对照组(p<0.0001)。综上所述,我们得出结论,GUMS16菌株的EPS除具有抗氧化活性外,还能够抑制K562细胞的生长。