Effects of Hyperglycemia and Doxorubicin on Aging Induction Optimization: Focus on the Role of p53 and mTOR in Human Dermal Fibroblast Cells

Dimas Adhi Pradita, None Achadiyani, Muhammad Hasan Bashari
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Abstract

Aging, a kind of physiological process, is influenced by a number of different biological and genetic factors, the driver for all age-related diseases. Aging of the skin can use samples of human fibroblasts (preputium) which are induced with high glucose media and doxorubicin using cell culture methods. Aging is measured using markers at the genetic level, namely p53 and mTOR. The p53 protein is one of the most important markers of apoptosis and the mTOR protein plays an important role in the proliferation, growth, motility, survival, autophagy of cell, including the synthesis of protein. Therefore, the optimization strategy of cell aging is well suited to physiological aging conditions In this review, we explore the optimization of aging in fibroblast cell cultures induced by high-glucose media and doxorubicin and review signs of aging, namely the biomarkers p53 and mTOR. The hope to be able to know aging is close to the original condition so that it becomes an opportunity as well as a challenge for the transition of basic research into developing interventions. Several major electronic databases, including Embase, PubMed, Cochrane, and CINAHL were used to select articles from the period between February 2013 and February 2023. From 5 available literatures, we demonstrated the activity of high-glucose media and doxorubicin as induction of fibroblast senescence. High-glucose media and doxorubicin showed an aging effect by increasing p53 and mTOR markers in fibroblast cell cultures. It is hoped that, with this article on aging optimization, insights into future research directions can be achieved.
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高血糖和阿霉素对衰老诱导优化的影响:关注p53和mTOR在人真皮成纤维细胞中的作用
衰老是一种生理过程,受到许多不同的生物和遗传因素的影响,是所有与年龄有关的疾病的驱动因素。老化的皮肤可以使用人类成纤维细胞(preputium)的样本,这是由高葡萄糖培养基和阿霉素用细胞培养方法诱导的。衰老是用基因水平的标记物来衡量的,即p53和mTOR。p53蛋白是细胞凋亡最重要的标志物之一,mTOR蛋白在细胞的增殖、生长、运动、存活、自噬,包括蛋白质的合成等过程中起着重要作用。因此,细胞衰老的优化策略非常适合生理衰老条件。本文探讨了高糖培养基和阿霉素诱导成纤维细胞衰老的优化,并综述了衰老的标志,即p53和mTOR的生物标志物。希望能够了解衰老接近于原始状态,从而使其成为基础研究向开发干预措施过渡的机遇和挑战。几个主要的电子数据库,包括Embase、PubMed、Cochrane和CINAHL,被用来选择2013年2月至2023年2月期间的文章。从现有的5篇文献中,我们证明了高糖培养基和阿霉素诱导成纤维细胞衰老的活性。高糖培养基和阿霉素通过增加成纤维细胞培养中的p53和mTOR标记物显示出衰老作用。希望通过本文对老龄化优化的研究,对未来的研究方向有所启发。
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