In vitro effects of ascorbic acid on viability and metabolism of patients' osteosarcoma stem cells.

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY Acta Pharmaceutica Pub Date : 2022-12-01 DOI:10.2478/acph-2022-0040
Marijana Šimić Jovičić, Maja Pušić, Maja Antunović, Maja Ledinski, Lucija Librenjak, Robert Kolundžić, Tomislav Ribičić, Vladimir Trkulja, Inga Urlić
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Abstract

Stagnation in novelties of osteosarcoma (OS) treatment indicates the need for new therapeutic methods. OS cancer stem cells (OS-CSC) are taught to have the ability to self-renew and develop mechanisms of anticancer drug resistance, and this is why it is difficult to eradicate them. Their metabolism has been recognized as a potential target of therapeutic action. Ascorbic acid (AA) is considered to act pro-oxidative against OS-CSC in vitro by oxidative effect and by inhibition of glycolysis. This study examined an in vitro impact of AA on OS-CSC metabolism isolated from patients' biopsies, with the aim of better understanding of OS-CSC metabolism and the action of AA on OS-CSC. OS-CSC were isolated using a sphere culture system and identified as stem cells using Hoechst 33342 exclusion assay. Determination of the dominant type of metabolism of OS-CSC, parental OS cells, human mesenchymal stem cells (hMSC) and U2OS OS lineage before and after AA treatment was done by Seahorse XF (Agilent). Cytotoxicity of high-dose AA was confirmed by the MTT test and was proven for all the examined cell types as well as HEK293. Seahorse technology showed that OS-CSC can potentially use both glycolysis and oxidative phosphorylation (OXPHOS), and can turn to glycolysis and slow metabolic potential in unfavorable conditions such as incubation in AA.

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体外抗坏血酸对骨肉瘤干细胞活力和代谢的影响。
骨肉瘤(OS)治疗新进展的停滞表明需要新的治疗方法。癌症干细胞(OS- csc)被认为具有自我更新的能力,并发展出抗癌耐药性机制,这就是为什么很难根除它们的原因。它们的代谢已被认为是治疗作用的潜在目标。抗坏血酸(AA)在体外通过氧化作用和抑制糖酵解作用,被认为对OS-CSC具有促氧化作用。本研究通过检测AA对患者活检分离的OS-CSC代谢的体外影响,旨在更好地了解OS-CSC代谢以及AA对OS-CSC的作用。采用球培养系统分离OS-CSC,采用Hoechst 33342排斥试验鉴定为干细胞。采用Seahorse XF (Agilent)检测AA处理前后OS- csc、亲代OS细胞、人间充质干细胞(hMSC)和U2OS OS系的优势代谢类型。MTT试验证实了高剂量AA的细胞毒性,并证实了对所有被检测细胞类型以及HEK293的细胞毒性。海马技术表明,OS-CSC可以同时使用糖酵解和氧化磷酸化(OXPHOS),并且可以在不利条件下(如在AA中孵育)转向糖酵解和缓慢代谢潜能。
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来源期刊
Acta Pharmaceutica
Acta Pharmaceutica PHARMACOLOGY & PHARMACY-
CiteScore
5.20
自引率
3.60%
发文量
20
审稿时长
>12 weeks
期刊介绍: AP is an international, multidisciplinary journal devoted to pharmaceutical and allied sciences and contains articles predominantly on core biomedical and health subjects. The aim of AP is to increase the impact of pharmaceutical research in academia, industry and laboratories. With strong emphasis on quality and originality, AP publishes reports from the discovery of a drug up to clinical practice. Topics covered are: analytics, biochemistry, biopharmaceutics, biotechnology, cell biology, cell cultures, clinical pharmacy, drug design, drug delivery, drug disposition, drug stability, gene technology, medicine (including diagnostics and therapy), medicinal chemistry, metabolism, molecular modeling, pharmacology (clinical and animal), peptide and protein chemistry, pharmacognosy, pharmacoepidemiology, pharmacoeconomics, pharmacodynamics and pharmacokinetics, protein design, radiopharmaceuticals, and toxicology.
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