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Multiple Functions of Lysyl Oxidase Like-2 in Oral Fibroproliferative Processes.赖氨酰氧化酶样蛋白 2 在口腔纤维增殖过程中的多种功能。
J Dent Res. 2018 Oct;97(11):1277-1284. doi: 10.1177/0022034518775971. Epub 2018 May 22.
2
Regulation of lysyl oxidase, collagen, and connective tissue growth factor by TGF-beta1 and detection in human gingiva.转化生长因子β1对赖氨酰氧化酶、胶原蛋白和结缔组织生长因子的调控及其在人牙龈中的检测
Lab Invest. 1999 Dec;79(12):1655-67.
3
Cytokine regulation of gingival fibroblast lysyl oxidase, collagen, and elastin.细胞因子对牙龈成纤维细胞赖氨酰氧化酶、胶原蛋白和弹性蛋白的调节
J Periodontol. 2002 Feb;73(2):145-52. doi: 10.1902/jop.2002.73.2.145.
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Significance of nuclear LOXL2 inhibition in fibroblasts and myofibroblasts in the fibrotic process of acute respiratory distress syndrome.核 LOXL2 抑制在急性呼吸窘迫综合征纤维化过程中纤维母细胞和肌成纤维细胞中的意义。
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Lysyl oxidase-like-2 (LOXL2) is a major isoform in chondrocytes and is critically required for differentiation.赖氨酰氧化酶样蛋白 2(LOXL2)是软骨细胞中的主要同工型,对于分化至关重要。
J Biol Chem. 2011 Jan 14;286(2):909-18. doi: 10.1074/jbc.M110.155622. Epub 2010 Nov 11.
6
Connective tissue growth factor in drug-induced gingival overgrowth.药物性牙龈增生中的结缔组织生长因子
J Periodontol. 2001 Jul;72(7):921-31. doi: 10.1902/jop.2001.72.7.921.
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Epithelial and connective tissue cell CTGF/CCN2 expression in gingival fibrosis.牙龈纤维化中上皮和结缔组织细胞的结缔组织生长因子/CCN2表达
J Pathol. 2006 Sep;210(1):59-66. doi: 10.1002/path.2000.
8
Phenytoin and cyclosporin A suppress the expression of MMP-1, TIMP-1, and cathepsin L, but not cathepsin B in cultured gingival fibroblasts.苯妥英钠和环孢素A可抑制培养的牙龈成纤维细胞中基质金属蛋白酶-1、金属蛋白酶组织抑制剂-1和组织蛋白酶L的表达,但不影响组织蛋白酶B的表达。
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Elevation of collagen type I in fibroblast-keratinocyte cocultures emphasizes the decisive role of fibroblasts in the manifestation of the phenotype of cyclosporin A-induced gingival overgrowth.成纤维细胞与角质形成细胞共培养体系中I型胶原蛋白水平的升高,凸显了成纤维细胞在环孢素A诱导的牙龈过度生长表型表现中的决定性作用。
J Periodontal Res. 2009 Feb;44(1):62-72. doi: 10.1111/j.1600-0765.2007.01066.x. Epub 2008 Oct 7.
10
LOXL2 Inhibition Paves the Way for Macrophage-Mediated Collagen Degradation in Liver Fibrosis.LOXL2 抑制为巨噬细胞介导的肝纤维化胶原降解铺平道路。
Front Immunol. 2020 Mar 31;11:480. doi: 10.3389/fimmu.2020.00480. eCollection 2020.

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Comparison of Immunohistochemical Markers in Oral Submucous Fibrosis and Oral Submucous Fibrosis Transformed to Oral Squamous Cell Carcinoma-A Systematic Review and Meta-Analysis.口腔黏膜下纤维性变和口腔黏膜下纤维性变转化为口腔鳞状细胞癌的免疫组织化学标志物比较:系统评价和荟萃分析。
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Lysyl Oxidase (LOX): Functional Contributions to Signaling Pathways.赖氨酰氧化酶(LOX):对信号通路的功能贡献。
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Mechanism for oral tumor cell lysyl oxidase like-2 in cancer development: synergy with PDGF-AB.口腔肿瘤细胞赖氨酰氧化酶样2在癌症发展中的机制:与血小板衍生生长因子AB的协同作用
Oncogenesis. 2019 May 13;8(5):34. doi: 10.1038/s41389-019-0144-0.

本文引用的文献

1
WITHDRAWN: PACE4 Proteolytically Processes LOXL2 with little impact on its catalytic activity.撤回:PACE4对LOXL2进行蛋白水解加工,对其催化活性影响较小。
J Biol Chem. 2017 Nov 28. doi: 10.1074/jbc.C117.810978.
2
Common oral complications of head and neck cancer radiation therapy: mucositis, infections, saliva change, fibrosis, sensory dysfunctions, dental caries, periodontal disease, and osteoradionecrosis.头颈部癌放射治疗常见的口腔并发症:黏膜炎、感染、唾液改变、纤维化、感觉功能障碍、龋齿、牙周疾病和放射性骨坏死。
Cancer Med. 2017 Dec;6(12):2918-2931. doi: 10.1002/cam4.1221. Epub 2017 Oct 25.
3
Proteolytic processing of lysyl oxidase-like-2 in the extracellular matrix is required for crosslinking of basement membrane collagen IV.基底膜胶原蛋白IV交联需要细胞外基质中赖氨酰氧化酶样蛋白2的蛋白水解加工。
J Biol Chem. 2017 Oct 13;292(41):16970-16982. doi: 10.1074/jbc.M117.798603. Epub 2017 Sep 1.
4
Prevention of phenytoin-induced gingival overgrowth by lovastatin in mice.洛伐他汀对小鼠苯妥英钠诱导的牙龈过度生长的预防作用
Am J Pathol. 2015 Jun;185(6):1588-99. doi: 10.1016/j.ajpath.2015.02.004. Epub 2015 Apr 2.
5
Molecular and clinical aspects of drug-induced gingival overgrowth.药物性牙龈增生的分子与临床方面
J Dent Res. 2015 Apr;94(4):540-6. doi: 10.1177/0022034515571265. Epub 2015 Feb 13.
6
LOXL2 catalytically inactive mutants mediate epithelial-to-mesenchymal transition.LOXL2 催化活性缺失突变体介导上皮-间充质转化。
Biol Open. 2014 Feb 15;3(2):129-37. doi: 10.1242/bio.20146841.
7
Collagen advanced glycation inhibits its Discoidin Domain Receptor 2 (DDR2)-mediated induction of lysyl oxidase in osteoblasts.胶原的高级糖基化抑制其在成骨细胞中诱导赖氨酰氧化酶的 Discoidin Domain Receptor 2 (DDR2)介导作用。
Bone. 2014 Jan;58:33-41. doi: 10.1016/j.bone.2013.10.001. Epub 2013 Oct 10.
8
Hepatocellular carcinoma cells cause different responses in expressions of cancer-promoting genes in different cancer-associated fibroblasts.肝癌细胞在不同的癌相关成纤维细胞中引起促进癌症发生的基因表达的不同反应。
Kaohsiung J Med Sci. 2013 Jun;29(6):312-8. doi: 10.1016/j.kjms.2012.08.012. Epub 2012 Oct 13.
9
The rationale for targeting the LOX family in cancer.靶向 LOX 家族治疗癌症的原理。
Nat Rev Cancer. 2012 Jul 19;12(8):540-52. doi: 10.1038/nrc3319.
10
Recombinant lysyl oxidase propeptide protein inhibits growth and promotes apoptosis of pre-existing murine breast cancer xenografts.重组赖氨酰氧化酶前肽蛋白抑制已存在的鼠乳腺癌异种移植物的生长并促进其凋亡。
PLoS One. 2012;7(2):e31188. doi: 10.1371/journal.pone.0031188. Epub 2012 Feb 8.

赖氨酰氧化酶样蛋白 2 在口腔纤维增殖过程中的多种功能。

Multiple Functions of Lysyl Oxidase Like-2 in Oral Fibroproliferative Processes.

机构信息

1 Department of Molecular and Cell Biology, Boston University Henry M. Goldman School of Dental Medicine, Boston, MA, USA.

2 Pharmaxis Ltd, Frenchs Forest NSW, Australia.

出版信息

J Dent Res. 2018 Oct;97(11):1277-1284. doi: 10.1177/0022034518775971. Epub 2018 May 22.

DOI:10.1177/0022034518775971
PMID:29787337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6151912/
Abstract

Gingival overgrowth is a side effect of certain medications, including calcium channel blockers, cyclosporin A, and phenytoin. Phenytoin-induced gingival overgrowth is fibrotic. Lysyl oxidases are extracellular enzymes that are required for biosynthetic cross-linking of collagens, and members of this enzyme family are upregulated in fibrosis. Previous studies in humans and in a mouse model of phenytoin-induced gingival overgrowth have shown that LOXL2 is elevated in the epithelium and connective tissue in gingival overgrowth tissues and not in normal tissues. Here, using a novel LOXL2 isoform-selective inhibitor and knockdown studies in loss- and gain-of-function studies, we investigated roles for LOXL2 in promoting cultures of human gingival fibroblasts to proliferate and to accumulate collagen. Data indicate that LOXL2 stimulates gingival fibroblast proliferation, likely by a platelet-derived growth factor B receptor-mediated mechanism. Moreover, collagen accumulation was stimulated by LOXL2 enzyme and inhibited by LOXL2 inhibitor or gene knockdown. These studies suggest that LOXL2 could serve as a potential therapeutic target to address oral fibrotic conditions.

摘要

牙龈增生是某些药物的副作用,包括钙通道阻滞剂、环孢素 A 和苯妥英钠。苯妥英钠引起的牙龈增生是纤维性的。赖氨酰氧化酶是细胞外酶,对于胶原蛋白的生物合成交联是必需的,该酶家族的成员在纤维化中上调。先前在人类和苯妥英钠诱导的牙龈过度生长的小鼠模型中的研究表明,LOXL2 在牙龈过度生长组织的上皮和结缔组织中升高,而在正常组织中不升高。在这里,我们使用一种新型的 LOXL2 同种型选择性抑制剂和基因敲低研究,在基因缺失和功能获得研究中,研究了 LOXL2 在促进人牙龈成纤维细胞增殖和积累胶原蛋白中的作用。数据表明,LOXL2 通过血小板衍生生长因子 B 受体介导的机制刺激牙龈成纤维细胞增殖。此外,胶原的积累被 LOXL2 酶刺激,并被 LOXL2 抑制剂或基因敲低抑制。这些研究表明,LOXL2 可以作为一种潜在的治疗靶点,用于解决口腔纤维性疾病。