Lodz University of Technology, Institute of Applied Radiation Chemistry, Laboratory of Laser Molecular Spectroscopy, Wroblewskiego 15, 93-590 Lodz, Poland.
Lodz University of Technology, Institute of Applied Radiation Chemistry, Laboratory of Laser Molecular Spectroscopy, Wroblewskiego 15, 93-590 Lodz, Poland.
Spectrochim Acta A Mol Biomol Spectrosc. 2022 Apr 5;270:120726. doi: 10.1016/j.saa.2021.120726. Epub 2021 Dec 17.
One of the most important areas of medical science is oncology, which is responsible for both the diagnostics and treatment of cancer diseases. Simultaneously one of the main challenges of oncology is the development of modern drugs effective in the fight against cancer. Statins are a group of biologically active compounds with the activity of 3-hydroxy-3-methyl glutaryl-CoA reductase inhibitors, an enzyme catalyzing the reduction of 3-hydroxy-3-methyl-glutaryl-CoA (HMG-CoA) to mevalonic acid. By acting on this enzyme, statins inhibit the endogenous cholesterol synthesis which in turn causes the reduction of its systemic concentrations. However, in vitro and in vivo studies confirm also the cytostatic and cytotoxic effects of statins against various types of cancer cells including colon cancer. In the presented studies the influence of mevastatin on cancerous colon cells CaCo-2 by Raman spectroscopy and imaging is discussed and compared with biochemistry characteristic for normal colon cells CCD-18Co. Based on vibrational features of colon cells: normal cells CCD-18Co, cancerous cells CaCo-2 and cancerous cells CaCo-2 treated by mevastatin in different concentrations and incubation times we have confirmed the influence of this statin on biochemistry composition of cancerous human colon cells. Moreover, the spectroscopic results for colon normal cells and cancerous cells based on data typical for nucleic acids, proteins, lipids have been compared. The cytotoxisity of mevastatin was determined by using XTT tests.
医学科学最重要的领域之一是肿瘤学,它负责癌症疾病的诊断和治疗。同时,肿瘤学的主要挑战之一是开发对抗癌症有效的现代药物。他汀类药物是一组具有 3-羟基-3-甲基戊二酰辅酶 A 还原酶抑制剂活性的生物活性化合物,该酶催化 3-羟基-3-甲基戊二酰辅酶 A(HMG-CoA)还原为甲羟戊酸。通过作用于这种酶,他汀类药物抑制内源性胆固醇合成,从而导致其系统浓度降低。然而,体外和体内研究也证实了他汀类药物对包括结肠癌在内的各种类型癌细胞的细胞抑制和细胞毒性作用。在目前的研究中,讨论了美伐他汀对癌细胞 CaCo-2 的拉曼光谱和成像的影响,并与正常结肠细胞 CCD-18Co 的生物化学特征进行了比较。基于结肠细胞的振动特征:正常细胞 CCD-18Co、癌细胞 CaCo-2 和用不同浓度和孵育时间的美伐他汀处理的癌细胞 CaCo-2,我们证实了这种他汀类药物对人结肠癌细胞生物化学组成的影响。此外,还比较了基于核酸、蛋白质、脂质典型数据的结肠正常细胞和癌细胞的光谱结果。使用 XTT 试验测定了美伐他汀的细胞毒性。