• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

SNHG12/NFYC-AS1 作为 hsa-miR-199a-5p 的海绵体促进 S100A8/S100A7/XDH 的表达并参与糖尿病足溃疡的进展。

SNHG12/NFYC-AS1 Acted as the Sponge for hsa-miR-199a-5p to Promote the Expression of S100A8/S100A7/XDH and was Involved in the Progression of Diabetic Foot Ulcers.

机构信息

Shuguang Hospital affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.

出版信息

Mol Biotechnol. 2023 Dec;65(12):2038-2048. doi: 10.1007/s12033-023-00692-4. Epub 2023 Mar 15.

DOI:10.1007/s12033-023-00692-4
PMID:36920714
Abstract

Traditional Chinese medicine has been used to treat diabetic foot ulcer (DFU) for a long time. However, the underlying mechanism of Radix arnebiae seu lithospermi ointment (RAS-ointment) has not been revealed. Effects of RAS-ointment treatment were observed in DFU patients. The endogenous competitive RNA mechanism was constructed based on micro-array sequencing and bioinformatics analysis. RT-PCR was used to detected the expression of genes in DFU ulcerated skins and non-ulcerated skins. Dual luciferase and RT-PCR experiments were used to investigate the endogenous competitive RNA mechanism. Based on micro-array sequencing and bioinformatics analysis, we found that SNHG12/NFYC-AS1, hsa-miR-199a-5p and S100A8/S100A7/XDH might form an endogenous competitive RNA mechanism. RT-PCR assay shown that SNHG12, NFYC-AS1, S100A8, S100A7 and XDH were significantly up-regulated, while hsa-miR-199a-5p was significantly down-regulated in DFU ulcerated skins (N = 10) compared with non-ulcerated skins (N = 10). Dual luciferase and RT-PCR experiments showed that SNHG12 or NFYC-AS1 up-regulated the expression of S100A8, S100A7 and XDH by inhibiting hsa-miR-199a-5p in a direct binding way. After 35 days of RAS-ointment treatment, the wound healing of DFU patients was substantially improved and the expression of S100A7 and XDH were reduced expression in DFU patients. In addition, the monomer composition of RAS-ointment, 49070_FLUKA or auraptenol inhibited the expression of S100A7 and XDH in Te317.sk cells. In conclusion, RAS-ointment may be used as an adjunctive therapy for DFU patients.

摘要

中药治疗糖尿病足溃疡(DFU)已有很长的历史。然而,紫草软膏(RAS-ointment)的作用机制尚未阐明。观察了 RAS-ointment 治疗 DFU 患者的效果。基于微阵列测序和生物信息学分析构建了内源性竞争 RNA 机制。用 RT-PCR 检测了 DFU 溃疡皮肤和非溃疡皮肤中基因的表达。使用双荧光素酶和 RT-PCR 实验研究了内源性竞争 RNA 机制。基于微阵列测序和生物信息学分析,我们发现 SNHG12/NFYC-AS1、hsa-miR-199a-5p 和 S100A8/S100A7/XDH 可能形成内源性竞争 RNA 机制。RT-PCR 检测表明,与非溃疡皮肤(N=10)相比,DFU 溃疡皮肤(N=10)中 SNHG12、NFYC-AS1、S100A8、S100A7 和 XDH 显著上调,而 hsa-miR-199a-5p 显著下调。双荧光素酶和 RT-PCR 实验表明,SNHG12 或 NFYC-AS1 通过直接结合抑制 hsa-miR-199a-5p 而上调 S100A8、S100A7 和 XDH 的表达。RAS-ointment 治疗 35 天后,DFU 患者的伤口愈合明显改善,DFU 患者 S100A7 和 XDH 的表达减少。此外,RAS-ointment 的单体成分 49070_FLUKA 或 auraptenol 抑制了 Te317.sk 细胞中 S100A7 和 XDH 的表达。总之,RAS-ointment 可作为 DFU 患者的辅助治疗。

相似文献

1
SNHG12/NFYC-AS1 Acted as the Sponge for hsa-miR-199a-5p to Promote the Expression of S100A8/S100A7/XDH and was Involved in the Progression of Diabetic Foot Ulcers.SNHG12/NFYC-AS1 作为 hsa-miR-199a-5p 的海绵体促进 S100A8/S100A7/XDH 的表达并参与糖尿病足溃疡的进展。
Mol Biotechnol. 2023 Dec;65(12):2038-2048. doi: 10.1007/s12033-023-00692-4. Epub 2023 Mar 15.
2
Up-regulated lncRNA-MSX2P1 promotes the growth of IL-22-stimulated keratinocytes by inhibiting miR-6731-5p and activating S100A7.上调的 lncRNA-MSX2P1 通过抑制 miR-6731-5p 和激活 S100A7 促进 IL-22 刺激的角质形成细胞的生长。
Exp Cell Res. 2018 Feb 15;363(2):243-254. doi: 10.1016/j.yexcr.2018.01.014. Epub 2018 Jan 13.
3
LncRNA DLEU1 promotes angiogenesis in diabetic foot ulcer wound healing by regulating miR-96-5p.长链非编码 RNA DLEU1 通过调节 miR-96-5p 促进糖尿病足溃疡创面愈合中的血管生成。
Ir J Med Sci. 2024 Feb;193(1):241-247. doi: 10.1007/s11845-023-03471-x. Epub 2023 Jul 29.
4
LncRNA SNHG16 Knockdown Promotes Diabetic Foot Ulcer Wound Healing via Sponging MiR-31-5p.LncRNA SNHG16 敲低通过海绵吸附 miR-31-5p 促进糖尿病足溃疡愈合。
Tohoku J Exp Med. 2023 Dec 23;261(4):283-289. doi: 10.1620/tjem.2023.J078. Epub 2023 Sep 14.
5
miR-199a-5p Plays a Pivotal Role on Wound Healing via Suppressing and in Diabetic Ulcer Foot.miR-199a-5p 通过抑制和在糖尿病溃疡足中发挥关键作用促进伤口愈合。
Oxid Med Cell Longev. 2022 Apr 7;2022:4791059. doi: 10.1155/2022/4791059. eCollection 2022.
6
Downregulation of hsa-miR-203 in peripheral blood and wound margin tissue by negative pressure wound therapy contributes to wound healing of diabetic foot ulcers.负压伤口疗法下调外周血和创面边缘组织中 hsa-miR-203 促进糖尿病足溃疡的愈合。
Microvasc Res. 2022 Jan;139:104275. doi: 10.1016/j.mvr.2021.104275. Epub 2021 Oct 28.
7
Expression of miR-217 and HIF-1α/VEGF pathway in patients with diabetic foot ulcer and its effect on angiogenesis of diabetic foot ulcer rats.miR-217 和 HIF-1α/VEGF 通路在糖尿病足溃疡患者中的表达及其对糖尿病足溃疡大鼠血管生成的影响。
J Endocrinol Invest. 2019 Nov;42(11):1307-1317. doi: 10.1007/s40618-019-01053-2. Epub 2019 May 11.
8
Silencing long non-coding RNAs nicotinamide nucleotide transhydrogenase antisense RNA 1 inhibited papillary thyroid cancer cell proliferation, migration and invasion and promoted apoptosis via targeting miR-199a-5p.沉默长链非编码 RNA 烟酰胺核苷酸转氢酶反义 RNA 1 通过靶向 miR-199a-5p 抑制甲状腺乳头状癌细胞增殖、迁移和侵袭并促进细胞凋亡。
Endocr J. 2021 May 28;68(5):583-597. doi: 10.1507/endocrj.EJ20-0353. Epub 2021 Mar 20.
9
MALAT1 participates in the role of platelet-rich plasma exosomes in promoting wound healing of diabetic foot ulcer.MALAT1 参与富血小板血浆外泌体在促进糖尿病足溃疡愈合中的作用。
Int J Biol Macromol. 2023 May 31;238:124170. doi: 10.1016/j.ijbiomac.2023.124170. Epub 2023 Mar 22.
10
Identifying potential pathogenesis and immune infiltration in diabetic foot ulcers using bioinformatics and in vitro analyses.运用生物信息学和体外分析方法鉴定糖尿病足溃疡的潜在发病机制和免疫浸润。
BMC Med Genomics. 2023 Dec 1;16(1):313. doi: 10.1186/s12920-023-01741-2.

引用本文的文献

1
Diabetic Wound Vasculopathy and Neuropathy: Spotlight on Wound Lipid Signaling.糖尿病伤口血管病变与神经病变:聚焦伤口脂质信号传导
Adv Wound Care (New Rochelle). 2025 Aug 13. doi: 10.1177/21621918251366681.
2
Machine learning combining external validation to explore the immunopathogenesis of diabetic foot ulcer and predict therapeutic drugs.结合外部验证的机器学习方法探索糖尿病足溃疡的免疫发病机制并预测治疗药物。
PLoS One. 2025 Aug 1;20(8):e0328906. doi: 10.1371/journal.pone.0328906. eCollection 2025.
3
The emerging modulators of non-coding RNAs in diabetic wound healing.

本文引用的文献

1
Invasive Liver Abscess Syndrome Caused by Carbapenem-Resistant Hypervirulent Klebsiella Pneumoniae: a Case Report.耐碳青霉烯类高毒力肺炎克雷伯菌引起的侵袭性肝脓肿综合征:一例报告
Clin Lab. 2022 Dec 1;68(12). doi: 10.7754/Clin.Lab.2022.220320.
2
Psychological interventions for treating foot ulcers, and preventing their recurrence, in people with diabetes.心理干预治疗糖尿病患者的足部溃疡及预防其复发。
Cochrane Database Syst Rev. 2021 Feb 8;2(2):CD012835. doi: 10.1002/14651858.CD012835.pub2.
3
Systematic Screening of Chemical Constituents in the Traditional Chinese Medicine by UHPLC-Q-Exactive Orbitrap Mass Spectrometry.
非编码 RNA 在糖尿病创面愈合中新兴的调控分子。
Front Endocrinol (Lausanne). 2024 Oct 8;15:1465975. doi: 10.3389/fendo.2024.1465975. eCollection 2024.
4
Identification of a shared gene signature and biological mechanism between diabetic foot ulcers and cutaneous lupus erythemnatosus by transcriptomic analysis.通过转录组分析鉴定糖尿病足溃疡和皮肤红斑狼疮之间共享的基因特征及生物学机制。
Front Physiol. 2024 Feb 16;15:1297810. doi: 10.3389/fphys.2024.1297810. eCollection 2024.
基于 UHPLC-Q-Exactive Orbitrap 质谱联用技术的中药化学成分系统筛选。
Molecules. 2022 Apr 19;27(9):2631. doi: 10.3390/molecules27092631.
4
Endothelial miR-199a-3p regulating cell adhesion molecules by targeting mTOR signaling during inflammation.炎症中内皮细胞 miR-199a-3p 通过靶向 mTOR 信号调节细胞黏附分子。
Eur J Pharmacol. 2022 Jun 15;925:174984. doi: 10.1016/j.ejphar.2022.174984. Epub 2022 Apr 28.
5
miR-199a-5p Plays a Pivotal Role on Wound Healing via Suppressing and in Diabetic Ulcer Foot.miR-199a-5p 通过抑制和在糖尿病溃疡足中发挥关键作用促进伤口愈合。
Oxid Med Cell Longev. 2022 Apr 7;2022:4791059. doi: 10.1155/2022/4791059. eCollection 2022.
6
Emerging Roles of Long Non-Coding RNAs in Diabetic Foot Ulcers.长链非编码RNA在糖尿病足溃疡中的新作用
Diabetes Metab Syndr Obes. 2021 Jun 9;14:2549-2560. doi: 10.2147/DMSO.S310566. eCollection 2021.
7
Macrophage polarization and diabetic wound healing.巨噬细胞极化与糖尿病创面愈合。
Transl Res. 2021 Oct;236:109-116. doi: 10.1016/j.trsl.2021.05.006. Epub 2021 Jun 2.
8
LncRNA GAS5 activates the HIF1A/VEGF pathway by binding to TAF15 to promote wound healing in diabetic foot ulcers.长链非编码 RNA GAS5 通过与 TAF15 结合激活 HIF1A/VEGF 通路,促进糖尿病足溃疡的伤口愈合。
Lab Invest. 2021 Aug;101(8):1071-1083. doi: 10.1038/s41374-021-00598-2. Epub 2021 Apr 19.
9
The Role of Oxidative Stress in Hyperuricemia and Xanthine Oxidoreductase (XOR) Inhibitors.氧化应激在高尿酸血症及黄嘌呤氧化酶(XOR)抑制剂中的作用。
Oxid Med Cell Longev. 2021 Mar 26;2021:1470380. doi: 10.1155/2021/1470380. eCollection 2021.
10
S100A7 promotes the development of human endometriosis by activating NF-κB signaling pathway in endometrial stromal cells.S100A7 通过激活子宫内膜基质细胞中的 NF-κB 信号通路促进人类子宫内膜异位症的发展。
Cell Biol Int. 2021 Jun;45(6):1327-1335. doi: 10.1002/cbin.11578. Epub 2021 Mar 19.