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相似文献

1
Autotaxin.自分泌运动因子
Cell Mol Life Sci. 2009 Sep;66(18):3009-21. doi: 10.1007/s00018-009-0056-9. Epub 2009 Jun 9.
2
Lysophosphatidic acids, cyclic phosphatidic acids and autotaxin as promising targets in therapies of cancer and other diseases.溶血磷脂酸、环磷酸酯酸和自分泌运动因子作为癌症及其他疾病治疗中颇具前景的靶点。
Acta Biochim Pol. 2008;55(2):227-40. Epub 2008 Jun 14.
3
[Secretion and role of autotaxin and lysophosphatidic acid in adipose tissue].[自分泌运动因子和溶血磷脂酸在脂肪组织中的分泌及作用]
J Soc Biol. 2006;200(1):77-81. doi: 10.1051/jbio:2006010.
4
Autotaxin, an ectoenzyme that produces lysophosphatidic acid, promotes the entry of lymphocytes into secondary lymphoid organs.自分泌运动因子是一种可产生溶血磷脂酸的胞外酶,它能促进淋巴细胞进入次级淋巴器官。
Nat Immunol. 2008 Apr;9(4):415-23. doi: 10.1038/ni1573. Epub 2008 Mar 9.
5
Lipid generation and signaling in ovarian cancer.卵巢癌中的脂质生成与信号传导。
Cancer Treat Res. 2009;149:241-67. doi: 10.1007/978-0-387-98094-2_12.
6
Autotaxin and lysophosphatidic acid stimulate intestinal cell motility by redistribution of the actin modifying protein villin to the developing lamellipodia.自分泌运动因子和溶血磷脂酸通过将肌动蛋白修饰蛋白绒毛蛋白重新分布到正在形成的片状伪足,来刺激肠道细胞运动。
Exp Cell Res. 2008 Feb 1;314(3):530-42. doi: 10.1016/j.yexcr.2007.10.028. Epub 2007 Nov 12.
7
High-fat diet, obesity and prostate disease: the ATX-LPA axis?高脂饮食、肥胖与前列腺疾病:自噬相关蛋白-溶血磷脂酸轴?
Nat Clin Pract Urol. 2009 Mar;6(3):128-31. doi: 10.1038/ncpuro1311. Epub 2009 Feb 10.
8
Autotaxin delays apoptosis induced by carboplatin in ovarian cancer cells.乙酰肝素酶延缓卡铂诱导的卵巢癌细胞凋亡。
Cell Signal. 2010 Jun;22(6):926-35. doi: 10.1016/j.cellsig.2010.01.017. Epub 2010 Jan 25.
9
Role of lysophosphatidic acid in the regulation of uterine leiomyoma cell proliferation by phospholipase D and autotaxin.溶血磷脂酸在磷脂酶D和自分泌运动因子调节子宫平滑肌瘤细胞增殖中的作用
J Lipid Res. 2008 Feb;49(2):295-307. doi: 10.1194/jlr.M700171-JLR200. Epub 2007 Nov 16.
10
Autotaxin is overexpressed in glioblastoma multiforme and contributes to cell motility of glioblastoma by converting lysophosphatidylcholine to lysophosphatidic acid.自分泌运动因子在多形性胶质母细胞瘤中过度表达,并通过将溶血磷脂酰胆碱转化为溶血磷脂酸促进胶质母细胞瘤的细胞运动。
J Biol Chem. 2006 Jun 23;281(25):17492-17500. doi: 10.1074/jbc.M601803200. Epub 2006 Apr 19.

引用本文的文献

1
Bronchopulmonary dysplasia demonstrates dysregulated autotaxin/lysophosphatidic acid signaling in a neonatal mouse model.在新生小鼠模型中,支气管肺发育不良表现出自分泌运动因子/溶血磷脂酸信号传导失调。
Pediatr Res. 2024 Oct 16. doi: 10.1038/s41390-024-03610-9.
2
Linking medicinal cannabis to autotaxin-lysophosphatidic acid signaling.将药用大麻与自分泌酶-溶血磷脂酸信号联系起来。
Life Sci Alliance. 2023 Jan 9;6(2). doi: 10.26508/lsa.202201595. Print 2023 Feb.
3
gene and autotaxin-lysophosphatidic acid axis in gastrointestinal cancers.胃肠道癌症中的基因与自分泌运动因子-溶血磷脂酸轴
World J Gastrointest Oncol. 2022 Aug 15;14(8):1388-1405. doi: 10.4251/wjgo.v14.i8.1388.
4
Lipoprotein(a), a Lethal Player in Calcific Aortic Valve Disease.脂蛋白(a),钙化性主动脉瓣疾病中的致命因素。
Front Cell Dev Biol. 2022 Jan 27;10:812368. doi: 10.3389/fcell.2022.812368. eCollection 2022.
5
Production of extracellular lysophosphatidic acid in the regulation of adipocyte functions and liver fibrosis.细胞外溶血磷脂酸的产生在调节脂肪细胞功能和肝纤维化中的作用。
World J Gastroenterol. 2018 Sep 28;24(36):4132-4151. doi: 10.3748/wjg.v24.i36.4132.
6
Doxycycline attenuates breast cancer related inflammation by decreasing plasma lysophosphatidate concentrations and inhibiting NF-κB activation.强力霉素通过降低血浆溶血磷脂酸浓度和抑制核因子κB激活来减轻乳腺癌相关炎症。
Mol Cancer. 2017 Feb 8;16(1):36. doi: 10.1186/s12943-017-0607-x.
7
Genome-wide analysis identifies colonic genes differentially associated with serum leptin and insulin concentrations in C57BL/6J mice fed a high-fat diet.全基因组分析确定了在高脂饮食喂养的C57BL/6J小鼠中,与血清瘦素和胰岛素浓度存在差异关联的结肠基因。
PLoS One. 2017 Feb 7;12(2):e0171664. doi: 10.1371/journal.pone.0171664. eCollection 2017.
8
Acute stress enhances the expression of neuroprotection- and neurogenesis-associated genes in the hippocampus of a mouse restraint model.急性应激增强了小鼠束缚模型海马体中与神经保护和神经发生相关基因的表达。
Oncotarget. 2016 Feb 23;7(8):8455-65. doi: 10.18632/oncotarget.7225.
9
Serum Autotaxin/ENPP2 correlates with insulin resistance in older humans with obesity.血清自分泌运动因子/胞外核苷酸焦磷酸酶/磷酸二酯酶2与老年肥胖人群的胰岛素抵抗相关。
Obesity (Silver Spring). 2015 Dec;23(12):2371-6. doi: 10.1002/oby.21232. Epub 2015 Nov 2.
10
Lysophosphatidic acid generation by pulmonary NKT cell ENPP-2/autotaxin exacerbates hyperoxic lung injury.肺NKT细胞的ENPP-2/自分泌运动因子产生溶血磷脂酸会加重高氧性肺损伤。
Purinergic Signal. 2015 Dec;11(4):455-61. doi: 10.1007/s11302-015-9463-6. Epub 2015 Aug 26.

本文引用的文献

1
Novel point mutations attenuate autotaxin activity.新型点突变减弱自分泌运动因子活性。
Lipids Health Dis. 2009 Feb 17;8:4. doi: 10.1186/1476-511X-8-4.
2
Repeatability of published microarray gene expression analyses.已发表的微阵列基因表达分析的可重复性。
Nat Genet. 2009 Feb;41(2):149-55. doi: 10.1038/ng.295. Epub 2008 Jan 28.
3
Autotaxin/lysopholipase D and lysophosphatidic acid regulate murine hemostasis and thrombosis.自分泌运动因子/溶血磷脂酶D和溶血磷脂酸调节小鼠的止血和血栓形成。
J Biol Chem. 2009 Mar 13;284(11):7385-94. doi: 10.1074/jbc.M807820200. Epub 2009 Jan 12.
4
Lysophosphatidic acid induces Ca2+ mobilization and c-Myc expression in mouse embryonic stem cells via the phospholipase C pathway.溶血磷脂酸通过磷脂酶C途径诱导小鼠胚胎干细胞中的Ca2+动员和c-Myc表达。
Cell Signal. 2009 Apr;21(4):523-8. doi: 10.1016/j.cellsig.2008.12.005. Epub 2008 Dec 24.
5
Lysophosphatidic acid (LPA) and its receptors.溶血磷脂酸(LPA)及其受体。
Curr Opin Pharmacol. 2009 Feb;9(1):15-23. doi: 10.1016/j.coph.2008.11.010. Epub 2008 Dec 30.
6
Autotaxin protects MCF-7 breast cancer and MDA-MB-435 melanoma cells against Taxol-induced apoptosis.自分泌运动因子可保护MCF-7乳腺癌细胞和MDA-MB-435黑色素瘤细胞免受紫杉醇诱导的凋亡。
Oncogene. 2009 Feb 19;28(7):1028-39. doi: 10.1038/onc.2008.442. Epub 2008 Dec 15.
7
Lipopolysaccharide induces autotaxin expression in human monocytic THP-1 cells.脂多糖诱导人单核细胞THP - 1细胞中自分泌运动因子的表达。
Biochem Biophys Res Commun. 2009 Jan 9;378(2):264-8. doi: 10.1016/j.bbrc.2008.11.047. Epub 2008 Nov 21.
8
Gene expression profiles of lysophosphatidic acid-related molecules in the prostate: relevance to prostate cancer and benign hyperplasia.前列腺中溶血磷脂酸相关分子的基因表达谱:与前列腺癌和良性增生的相关性。
Prostate. 2009 Feb 15;69(3):283-92. doi: 10.1002/pros.20879.
9
Simultaneous stimulation of spinal NK1 and NMDA receptors produces LPC which undergoes ATX-mediated conversion to LPA, an initiator of neuropathic pain.同时刺激脊髓中的NK1和NMDA受体可产生溶血磷脂酰胆碱(LPC),其经自分泌运动因子(ATX)介导转化为溶血磷脂酸(LPA),即神经性疼痛的引发剂。
J Neurochem. 2008 Dec;107(6):1556-65. doi: 10.1111/j.1471-4159.2008.05725.x. Epub 2008 Nov 5.
10
Inhibition of invasion and metastasis of hepatocellular carcinoma cells via targeting RhoC in vitro and in vivo.通过在体外和体内靶向RhoC抑制肝癌细胞的侵袭和转移
Clin Cancer Res. 2008 Nov 1;14(21):6804-12. doi: 10.1158/1078-0432.CCR-07-4820.

自分泌运动因子

Autotaxin.

作者信息

Boutin Jean A, Ferry Gilles

机构信息

Pharmacologie Moléculaire et Cellulaire, Institut de Recherches SERVIER, Croissy-sur-Seine, France.

出版信息

Cell Mol Life Sci. 2009 Sep;66(18):3009-21. doi: 10.1007/s00018-009-0056-9. Epub 2009 Jun 9.

DOI:10.1007/s00018-009-0056-9
PMID:19506801
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11115523/
Abstract

Autotaxin is a protein of approximately 900 amino acids discovered in the early 1990s. Over the past 15 years, a strong association between cancer cells and autotaxin production has been observed. Recent publications indicate that autotaxin and the capacity of cancer to metastasise are intimately linked. The discovery of new molecular targets in pharmacology is a mixture of pure luck, hard work and industrial strategy. Despite a crucial and desperate need for new therapeutic tools, many targets are approached in oncology, but only a few are validated and end up at the patient bed. Outside the busy domain of kinases, few targets have been discovered that can be useful in treating cancer, particularly metastatic processes. The fortuitous relationship between autotaxin and lysophosphatidic acid renders the results of observations made in the diabetes/obesity context considerably important. The literature provides observations that may aid in redesigning experiments to validate autotaxin as a potential oncology target.

摘要

自分泌运动因子是一种在20世纪90年代初发现的由大约900个氨基酸组成的蛋白质。在过去15年里,人们观察到癌细胞与自分泌运动因子的产生之间存在紧密联系。最近的出版物表明,自分泌运动因子与癌症转移能力密切相关。药理学中新分子靶点的发现是纯粹运气、辛勤工作和产业策略的结合。尽管迫切需要新的治疗工具,但肿瘤学中有许多靶点被研究,但只有少数得到验证并最终应用于患者治疗。在激酶这个热门领域之外,很少发现可用于治疗癌症(特别是转移过程)的靶点。自分泌运动因子与溶血磷脂酸之间的偶然关系使得在糖尿病/肥胖背景下所做观察结果相当重要。文献提供的观察结果可能有助于重新设计实验,以验证自分泌运动因子作为潜在肿瘤学靶点的作用。