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光疗对糖尿病和正常人皮肤成纤维细胞癌症易感基因的影响。

The Effect of Phototherapy on Cancer Predisposition Genes of Diabetic and Normal Human Skin Fibroblasts.

作者信息

Chotikasemsri Pongsathorn, Tangtrakulwanich Boonsin, Sangkhathat Surasak

机构信息

Biomedical Engineering Institute, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla, Thailand.

Department of Orthopedic Surgery and Physical Medicine, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla, Thailand.

出版信息

Biomed Res Int. 2017;2017:7604861. doi: 10.1155/2017/7604861. Epub 2017 Mar 12.

DOI:10.1155/2017/7604861
PMID:28386563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5366218/
Abstract

The purpose of this study was to investigate whether LED light at different wavelengths affects the expression profile of 143 cancer predisposition genes in both diabetic and normal human fibroblasts. In this study, both diabetic and normal fibroblast cell lines were cultured and irradiated with red (635 nm), green (520 nm), and blue (465 nm) LED light for 10 minutes at 0.67 J/cm each. After that, mRNA from all cell lines was extracted for microarray analysis. We found that green light activates EPHB2, KIT, ANTXR2, ESCO2, MSR1, EXT1, TSC1, KIT, NF1, BUB1B, FANCD2, EPCAM, FANCD2, NF, DIS3L2, and RET in normal fibroblast cells, while blue and red light can upregulate RUNX1, PDGFRA, EHBP1, GPC3, AXIN2, KDR, GLMN, MSMB, EPHB2, MSR1, KIT, FANCD2, BMPR1A, BUB1B, PDE11A, and RET. Therefore, genetic screening before phototherapy treatment may be required.

摘要

本研究的目的是调查不同波长的LED光是否会影响糖尿病患者和正常人成纤维细胞中143种癌症易感基因的表达谱。在本研究中,培养糖尿病和成纤维细胞系,并用红色(635nm)、绿色(520nm)和蓝色(465nm)LED光以0.67J/cm²的强度照射10分钟。之后,提取所有细胞系的mRNA进行微阵列分析。我们发现,绿光可激活正常成纤维细胞中的EPHB2、KIT、ANTXR2、ESCO2、MSR1、EXT1、TSC1、KIT、NF1、BUB1B、FANCD2、EPCAM、FANCD2、NF、DIS3L2和RET,而蓝光和红光可上调RUNX1、PDGFRA、EHBP1、GPC3、AXIN2、KDR、GLMN、MSMB、EPHB2、MSR1、KIT、FANCD2、BMPR1A、BUB1B、PDE11A和RET。因此,光疗前可能需要进行基因筛查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c255/5366218/4c629130ad6d/BMRI2017-7604861.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c255/5366218/d58ce180ebad/BMRI2017-7604861.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c255/5366218/4c629130ad6d/BMRI2017-7604861.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c255/5366218/d58ce180ebad/BMRI2017-7604861.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c255/5366218/4c629130ad6d/BMRI2017-7604861.002.jpg

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本文引用的文献

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2
Can Big Data Shed Light on the Origins of Pediatric Cancer?大数据能揭示儿童癌症的起源吗?
Pediatrics. 2016 Jun;137(6). doi: 10.1542/peds.2016-0983.
3
Neonatal Phototherapy and Infantile Cancer.新生儿光疗与儿童癌症
Pediatrics. 2016 Jun;137(6). doi: 10.1542/peds.2015-1353.
4
p53 family members - important messengers in cell death signaling in photodynamic therapy of cancer?p53家族成员——癌症光动力治疗中细胞死亡信号传导的重要信使?
Photochem Photobiol Sci. 2015 Aug;14(8):1390-6. doi: 10.1039/c5pp00251f. Epub 2015 Jul 23.
5
Expression of proapoptotic BAX and TP53 genes and antiapoptotic BCL-2 gene in MCF-7 and T-47D tumour cell cultures of the mammary gland after a photodynamic therapy with photolon.在用Photolon进行光动力治疗后,乳腺MCF-7和T-47D肿瘤细胞培养物中促凋亡BAX和TP53基因以及抗凋亡BCL-2基因的表达。
Adv Clin Exp Med. 2015 Jan-Feb;24(1):37-46. doi: 10.17219/acem/38152.