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体外分析皮肤原位癌化中的细胞分化、氧化应激、炎症和 DNA 损伤。

Ex Vivo Analysis of Cell Differentiation, Oxidative Stress, Inflammation, and DNA Damage on Cutaneous Field Cancerization.

机构信息

Department of Health Sciences, University of Eastern Piedmont, Via Paolo Solaroli 17, 28100 Novara, Italy.

AOU Maggiore della Carità di Novara, c.so Mazzini 18, 28100 Novara, Italy.

出版信息

Int J Mol Sci. 2024 May 26;25(11):5775. doi: 10.3390/ijms25115775.

Abstract

Cutaneous field cancerization (CFC) refers to a skin region containing mutated cells' clones, predominantly arising from chronic exposure to ultraviolet radiation (UVR), which exhibits an elevated risk of developing precancerous and neoplastic lesions. Despite extensive research, many molecular aspects of CFC still need to be better understood. In this study, we conducted ex vivo assessment of cell differentiation, oxidative stress, inflammation, and DNA damage in CFC samples. We collected perilesional skin from 41 patients with skin cancer and non-photoexposed skin from 25 healthy control individuals. These biopsies were either paraffin-embedded for indirect immunofluorescence and immunohistochemistry stain or processed for proteins and mRNA extraction from the epidermidis. Our findings indicate a downregulation of p53 expression and an upregulation of Ki67 and p16 in CFC tissues. Additionally, there were alterations in keratinocyte differentiation markers, disrupted cell differentiation, increased expression of iNOS and proinflammatory cytokines IL-6 and IL-8, along with evidence of oxidative DNA damage. Collectively, our results suggest that despite its outwardly normal appearance, CFC tissue shows early signs of DNA damage, an active inflammatory state, oxidative stress, abnormal cell proliferation and differentiation.

摘要

皮肤区域性癌前病变(CFC)是指一个皮肤区域含有突变细胞的克隆,主要由慢性暴露于紫外线辐射(UVR)引起,其具有发展为癌前和肿瘤病变的高风险。尽管进行了广泛的研究,但 CFC 的许多分子方面仍需要更好地理解。在这项研究中,我们对 CFC 样本中的细胞分化、氧化应激、炎症和 DNA 损伤进行了离体评估。我们从 41 名皮肤癌患者的病变周围皮肤和 25 名健康对照个体的非光暴露皮肤中采集了活检样本。这些活检标本要么被石蜡包埋用于间接免疫荧光和免疫组织化学染色,要么被处理用于从表皮中提取蛋白质和 mRNA。我们的研究结果表明,CFC 组织中 p53 表达下调,Ki67 和 p16 表达上调。此外,角蛋白细胞分化标志物发生改变,细胞分化受到干扰,诱导型一氧化氮合酶(iNOS)和促炎细胞因子白细胞介素-6(IL-6)和白细胞介素-8(IL-8)的表达增加,同时存在氧化 DNA 损伤的证据。总的来说,我们的结果表明,尽管 CFC 组织表面看起来正常,但它已经出现了 DNA 损伤、活跃的炎症状态、氧化应激、异常细胞增殖和分化的早期迹象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d643/11171589/bfdff0888aa8/ijms-25-05775-g001.jpg

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