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一组与血管生成、抗氧化防御和缺氧相关的潜在血清标志物,用于区分皮肤鳞状细胞癌和光化性角化病。

A Panel of Potential Serum Markers Related to Angiogenesis, Antioxidant Defense and Hypoxia for Differentiating Cutaneous Squamous Cell Carcinomas from Actinic Keratoses.

作者信息

Georgescu Simona Roxana, Tocut Sandra Milena, Matei Clara, Ene Corina Daniela, Nicolae Ilinca, Tampa Mircea

机构信息

Department of Dermatology, 'Carol Davila' University of Medicine and Pharmacy, 020021 Bucharest, Romania.

Department of Dermatology, 'Victor Babes' Clinical Hospital for Infectious Diseases, 030303 Bucharest, Romania.

出版信息

J Pers Med. 2024 Jan 17;14(1):103. doi: 10.3390/jpm14010103.

DOI:10.3390/jpm14010103
PMID:38248804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10820834/
Abstract

Cutaneous squamous cell carcinoma (cSCC) arising from the malignant proliferation of epidermal keratinocytes is the second most common skin cancer. Actinic keratosis (AK), which is considered cSCC in situ, may progress into invasive tumors. Currently, there are no serum markers that can differentiate cSCC from AK. The aim of our study was to assess angiogenesis and oxidative stress in patients with cSCC and patients with AK and find reliable serum markers useful in the diagnosis of cSCC. We have determined the serum levels of a group of proangiogenic factors (MMP-2, MMP-9, VEGF, FGF2), the total antioxidative status/capacity (TAS/TAC), ImAnOx, a marker of oxidative stress, and HIF-1 alpha, an indicator of hypoxia. We have identified higher serum levels of MMP-2. MMP-9, VEGF, FGF2 and HIF-1 alpha and lower levels of ImAnOx in cSCC patients compared to AK patients and controls. There were no statistically significant differences between AK patients and controls. We have found positive correlations between proangiogenic markers and HIF-1 alpha and negative correlations between proangiogenic markers and ImAnOx. Our results suggest that MMP-2, MMP-9, VEGF, FGF2, ImAnOx and HIF-1 may be promising markers for differentiating AK from cSCC, and there is a link between angiogenesis, oxidative stress and hypoxia.

摘要

由表皮角质形成细胞恶性增殖引起的皮肤鳞状细胞癌(cSCC)是第二常见的皮肤癌。光化性角化病(AK)被认为是原位cSCC,可能会发展为浸润性肿瘤。目前,尚无能够区分cSCC和AK的血清标志物。我们研究的目的是评估cSCC患者和AK患者的血管生成和氧化应激,并找到对cSCC诊断有用的可靠血清标志物。我们测定了一组促血管生成因子(MMP-2、MMP-9、VEGF、FGF2)的血清水平、总抗氧化状态/能力(TAS/TAC)、氧化应激标志物ImAnOx以及缺氧指标HIF-1α。我们发现,与AK患者和对照组相比,cSCC患者的血清MMP-2、MMP-9、VEGF、FGF2和HIF-1α水平较高,而ImAnOx水平较低。AK患者和对照组之间无统计学显著差异。我们发现促血管生成标志物与HIF-1α之间呈正相关,促血管生成标志物与ImAnOx之间呈负相关。我们的结果表明,MMP-2、MMP-9、VEGF、FGF2、ImAnOx和HIF-1可能是区分AK和cSCC的有前景的标志物,并且血管生成、氧化应激和缺氧之间存在联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e201/10820834/f7ad06d677ab/jpm-14-00103-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e201/10820834/fe5a37108a93/jpm-14-00103-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e201/10820834/f7ad06d677ab/jpm-14-00103-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e201/10820834/fe5a37108a93/jpm-14-00103-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e201/10820834/f7ad06d677ab/jpm-14-00103-g002.jpg

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FGFR2c Upregulation Contributes to Cancer-Associated Fibroblast Program Activation and to Enhanced Autophagy in Actinic Keratosis-Derived Dermal Fibroblasts: A Possible Role in Precancerous Cell/Stromal Cell Crosstalk.FGFR2c上调促成光化性角化病来源的真皮成纤维细胞中癌症相关成纤维细胞程序激活及自噬增强:在癌前细胞/基质细胞串扰中的可能作用
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