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整合 RNA 测序和微阵列分析鉴定 UVB 暴露对人皮肤的不良影响。

Integrative analysis of RNA-sequencing and microarray for the identification of adverse effects of UVB exposure on human skin.

机构信息

Department of Life Science, Institute of Environmental Medicine for Green Chemistry, Dongguk University Biomedi Campus, Gyeonggi-do, Republic of Korea.

Research and Innovation Center, Amorepacific, Gyeonggi-do, Republic of Korea.

出版信息

Front Public Health. 2024 Feb 20;12:1328089. doi: 10.3389/fpubh.2024.1328089. eCollection 2024.

DOI:10.3389/fpubh.2024.1328089
PMID:38444441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10913594/
Abstract

BACKGROUND

Ultraviolet B (UVB) from sunlight represents a major environmental factor that causes toxic effects resulting in structural and functional cutaneous abnormalities in most living organisms. Although numerous studies have indicated the biological mechanisms linking UVB exposure and cutaneous manifestations, they have typically originated from a single study performed under limited conditions.

METHODS

We accessed all publicly accessible expression data of various skin cell types exposed to UVB, including skin biopsies, keratinocytes, and fibroblasts. We performed biological network analysis to identify the molecular mechanisms and identify genetic biomarkers.

RESULTS

We interpreted the inflammatory response and carcinogenesis as major UVB-induced signaling alternations and identified three candidate biomarkers (, , and ). Moreover, we confirmed that these three biomarkers contribute to the survival probability of patients with cutaneous melanoma, the most aggressive and lethal form of skin cancer.

CONCLUSION

Our findings will aid the understanding of UVB-induced cutaneous toxicity and the accompanying molecular mechanisms. In addition, the three candidate biomarkers that change molecular signals due to UVB exposure of skin might be related to the survival rate of patients with cutaneous melanoma.

摘要

背景

阳光中的紫外线 B(UVB)是导致大多数生物出现结构和功能皮肤异常的主要环境因素,具有毒性作用。虽然许多研究表明了紫外线 B 暴露与皮肤表现之间的生物学机制,但这些研究通常来自于在有限条件下进行的单一研究。

方法

我们获取了所有可公开访问的各种皮肤细胞类型暴露于 UVB 的表达数据,包括皮肤活检、角质形成细胞和成纤维细胞。我们进行了生物网络分析,以确定分子机制并识别遗传生物标志物。

结果

我们将炎症反应和癌变解释为主要的 UVB 诱导信号改变,并鉴定出三个候选生物标志物(、和)。此外,我们还证实这三个生物标志物与皮肤黑色素瘤患者的生存概率有关,皮肤黑色素瘤是最具侵袭性和致命性的皮肤癌。

结论

我们的研究结果将有助于理解 UVB 诱导的皮肤毒性及其伴随的分子机制。此外,由于皮肤暴露于 UVB 而改变分子信号的三个候选生物标志物可能与皮肤黑色素瘤患者的生存率有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f78/10913594/245b3c79035b/fpubh-12-1328089-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f78/10913594/e3e325686390/fpubh-12-1328089-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f78/10913594/da4b9e69f314/fpubh-12-1328089-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f78/10913594/245b3c79035b/fpubh-12-1328089-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f78/10913594/e3e325686390/fpubh-12-1328089-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f78/10913594/da4b9e69f314/fpubh-12-1328089-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f78/10913594/245b3c79035b/fpubh-12-1328089-g003.jpg

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本文引用的文献

1
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Environ Toxicol. 2022 Dec;37(12):2897-2909. doi: 10.1002/tox.23646. Epub 2022 Sep 5.
2
Integrative transcriptome-wide analysis of atopic dermatitis for drug repositioning.特应性皮炎的综合转录组全基因组分析,用于药物重定位。
Commun Biol. 2022 Jun 22;5(1):615. doi: 10.1038/s42003-022-03564-w.
3
Inhibition of Fibroblast Growth Factor Receptor Attenuates UVB-Induced Skin Carcinogenesis.
抑制成纤维细胞生长因子受体可减轻 UVB 诱导的皮肤癌变。
J Invest Dermatol. 2022 Nov;142(11):2873-2884.e7. doi: 10.1016/j.jid.2022.03.036. Epub 2022 May 10.
4
Evaluation of Biological Effects and Transcriptome Changes Induced by LED-Based Narrow-Band UVB Phototherapy.基于 LED 的窄带 UVB 光疗诱导的生物学效应和转录组变化的评估。
Photochem Photobiol. 2022 Nov;98(6):1379-1389. doi: 10.1111/php.13643. Epub 2022 May 30.
5
Survival Genie, a web platform for survival analysis across pediatric and adult cancers.Survival Genie,一个跨儿科和成人癌症的生存分析的网络平台。
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6
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Acta Pharm Sin B. 2022 Jan;12(1):339-352. doi: 10.1016/j.apsb.2021.07.019. Epub 2021 Jul 26.
7
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8
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9
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Biosci Rep. 2020 Nov 27;40(11). doi: 10.1042/BSR20202911.