• 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

相似文献

1
Elevated levels of CXC chemokine connective tissue activating peptide (CTAP)-III in lung cancer patients.肺癌患者中CXC趋化因子结缔组织激活肽(CTAP)-III水平升高。
Am J Transl Res. 2011 May 15;3(3):226-33. Epub 2011 Apr 2.
2
Connective tissue-activating peptide III: a novel blood biomarker for early lung cancer detection.结缔组织激活肽III:一种用于早期肺癌检测的新型血液生物标志物。
J Clin Oncol. 2009 Jun 10;27(17):2787-92. doi: 10.1200/JCO.2008.19.4233. Epub 2009 May 4.
3
Platelet-derived chemokines CXC chemokine ligand (CXCL)7, connective tissue-activating peptide III, and CXCL4 differentially affect and cross-regulate neutrophil adhesion and transendothelial migration.血小板衍生的趋化因子CXC趋化因子配体(CXCL)7、结缔组织激活肽III和CXCL4对中性粒细胞的黏附和跨内皮迁移有不同影响并相互交叉调节。
J Immunol. 2002 Sep 1;169(5):2602-10. doi: 10.4049/jimmunol.169.5.2602.
4
Connective tissue activation. XXXVI. The origin, variety, distribution, and biologic fate of connective tissue activating peptide-III isoforms: characteristics in patients with rheumatic, renal, and arterial disease.结缔组织激活。XXXVI. 结缔组织激活肽-III 亚型的起源、种类、分布及生物学命运:风湿性、肾脏及动脉疾病患者的特征
Arthritis Rheum. 1993 Aug;36(8):1142-53. doi: 10.1002/art.1780360816.
5
Connective tissue-activating peptide III desensitizes chemokine receptors on neutrophils. Requirement for proteolytic formation of the neutrophil-activating peptide 2.结缔组织激活肽III使中性粒细胞上的趋化因子受体脱敏。中性粒细胞激活肽2的蛋白水解形成的必要性。
J Immunol. 1994 Dec 15;153(12):5698-708.
6
Megakaryocyte maturation is associated with expression of the CXC chemokine connective tissue-activating peptide CTAP III.巨核细胞成熟与CXC趋化因子结缔组织激活肽CTAP III的表达相关。
Br J Haematol. 2000 Dec;111(4):1180-9. doi: 10.1046/j.1365-2141.2000.02476.x.
7
Regulation of glucose transporters by connective tissue activating peptide-III isoforms.结缔组织激活肽-III 亚型对葡萄糖转运蛋白的调节作用。
J Biol Chem. 1992 Sep 25;267(27):19579-86.
8
Down-regulation of neutrophil functions by the ELR(+) CXC chemokine platelet basic protein.ELR(+) CXC趋化因子血小板碱性蛋白对中性粒细胞功能的下调作用
Blood. 2000 Nov 1;96(9):2965-72.
9
Novel C-terminally truncated isoforms of the CXC chemokine beta-thromboglobulin and their impact on neutrophil functions.CXC趋化因子β-血小板球蛋白的新型C末端截短异构体及其对中性粒细胞功能的影响。
J Immunol. 1998 Nov 1;161(9):4975-82.
10
Mast cells and neutrophils proteolytically activate chemokine precursor CTAP-III and are subject to counterregulation by PF-4 through inhibition of chymase and cathepsin G.肥大细胞和中性粒细胞通过蛋白水解作用激活趋化因子前体CTAP-III,并且PF-4可通过抑制糜蛋白酶和组织蛋白酶G对其进行反向调节。
Blood. 2006 Mar 15;107(6):2234-42. doi: 10.1182/blood-2005-06-2424. Epub 2005 Nov 29.

引用本文的文献

1
Multifaceted Roles of Chemokine C-X-C Motif Ligand 7 in Inflammatory Diseases and Cancer.趋化因子C-X-C基序配体7在炎症性疾病和癌症中的多方面作用
Front Pharmacol. 2022 Jun 28;13:914730. doi: 10.3389/fphar.2022.914730. eCollection 2022.
2
Oxymatrine inhibits the development of non-small cell lung cancer through miR-367-3p upregulation and target gene downregulation.氧化苦参碱通过上调miR-367-3p和下调靶基因来抑制非小细胞肺癌的发展。
Am J Transl Res. 2020 Sep 15;12(9):5538-5550. eCollection 2020.
3
Overexpression of golgi membrane protein 1 promotes non-small-cell carcinoma aggressiveness by regulating the matrix metallopeptidase 13.高尔基体膜蛋白1的过表达通过调节基质金属肽酶13促进非小细胞癌的侵袭性。
Am J Cancer Res. 2018 Mar 1;8(3):551-565. eCollection 2018.
4
CTAPIII/CXCL7: a novel biomarker for early diagnosis of lung cancer.CTAPIII/CXCL7:一种用于肺癌早期诊断的新型生物标志物。
Cancer Med. 2018 Feb;7(2):325-335. doi: 10.1002/cam4.1292. Epub 2018 Jan 22.
5
Role of platelet chemokines, PF-4 and CTAP-III, in cancer biology.血小板趋化因子、PF-4 和 CTAP-III 在癌症生物学中的作用。
J Hematol Oncol. 2013 Jun 24;6:42. doi: 10.1186/1756-8722-6-42.

本文引用的文献

1
Breast cancer stem cells are regulated by mesenchymal stem cells through cytokine networks.乳腺癌干细胞受间充质干细胞通过细胞因子网络调控。
Cancer Res. 2011 Jan 15;71(2):614-24. doi: 10.1158/0008-5472.CAN-10-0538. Epub 2011 Jan 11.
2
Proteomic characterization of human early pro-angiogenic cells.人类早期血管生成前体细胞的蛋白质组学特征分析。
J Mol Cell Cardiol. 2011 Feb;50(2):333-6. doi: 10.1016/j.yjmcc.2010.11.022. Epub 2010 Dec 13.
3
The National Lung Screening Trial: overview and study design.国家肺癌筛查试验:概述与研究设计。
Radiology. 2011 Jan;258(1):243-53. doi: 10.1148/radiol.10091808. Epub 2010 Nov 2.
4
A chronic obstructive pulmonary disease related signature in squamous cell lung cancer.鳞状细胞肺癌中的慢性阻塞性肺疾病相关特征。
Lung Cancer. 2011 May;72(2):177-83. doi: 10.1016/j.lungcan.2010.08.014. Epub 2010 Sep 15.
5
Cancer statistics, 2010.癌症统计数据,2010 年。
CA Cancer J Clin. 2010 Sep-Oct;60(5):277-300. doi: 10.3322/caac.20073. Epub 2010 Jul 7.
6
Chronic obstructive pulmonary disease and altered risk of lung cancer in a population-based case-control study.基于人群的病例对照研究中慢性阻塞性肺疾病与肺癌风险改变的关系。
PLoS One. 2009 Oct 8;4(10):e7380. doi: 10.1371/journal.pone.0007380.
7
Functional activity of CXCL8 receptors, CXCR1 and CXCR2, on human malignant melanoma progression.CXCL8受体CXCR1和CXCR2的功能活性对人类恶性黑色素瘤进展的影响
Eur J Cancer. 2009 Sep;45(14):2618-27. doi: 10.1016/j.ejca.2009.07.007. Epub 2009 Aug 13.
8
Lung function predicts lung cancer risk in smokers: a tool for targeting screening programmes.肺功能可预测吸烟者的肺癌风险:一种用于定位筛查计划的工具。
Eur Respir J. 2010 Jan;35(1):146-51. doi: 10.1183/09031936.00049909. Epub 2009 Aug 13.
9
Systemic inflammatory markers in COPD: results from the Bergen COPD Cohort Study.COPD 中的系统性炎症标志物:来自卑尔根 COPD 队列研究的结果。
Eur Respir J. 2010 Mar;35(3):540-8. doi: 10.1183/09031936.00088209. Epub 2009 Jul 30.
10
Chronic inflammation, chronic obstructive pulmonary disease, and lung cancer.慢性炎症、慢性阻塞性肺疾病和肺癌。
Curr Opin Pulm Med. 2009 Jul;15(4):303-7. doi: 10.1097/MCP.0b013e32832c975a.

肺癌患者中CXC趋化因子结缔组织激活肽(CTAP)-III水平升高。

Elevated levels of CXC chemokine connective tissue activating peptide (CTAP)-III in lung cancer patients.

作者信息

Lee Gina, Gardner Brian K, Elashoff David A, Purcell Colleen M, Sandha Harpavan S, Mao Jenny T, Krysan Kostyantyn, Lee Jay M, Dubinett Steven M

出版信息

Am J Transl Res. 2011 May 15;3(3):226-33. Epub 2011 Apr 2.

PMID:21654877
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3102566/
Abstract

Despite advances in treatments, lung cancer has been the leading cause of cancer-related deaths in the United States for the past several decades. Recent findings from the National Lung Screening Trial reveal that low-dose helical computed tomography (CT) scan screening of high-risk individuals reduces lung cancer mortality. This suggests that early detection is of key importance to improving patient outcome. However, of those screened with CT scans, 25% had positive scans that require further follow-up studies which often involve more radiation exposure and invasive tests to reduce false positive results. The purpose of this study was to identify candidate plasma biomarkers to aid in diagnosis of lung cancer in at-risk individuals. We found increased expression of the CXC chemokine connective tissue-activating peptide (CTAP)-III from plasma specimens of lung cancer patients compared to at-risk control subjects. Identification of the peptide was confirmed by the addition of an anti-NAP-2 antibody that recognizes CTAP-III and NAP-2. We also quantified and verified the increased levels of plasma CTAP-III with ELISA in patients with lung cancer (mean ± SD, 1859 ± 1219 ng/mL) compared to controls (698 ± 434 ng/mL; P<0.001). Our findings demonstrate elevated plasma levels of CTAP-III occur in lung cancer patients. Further studies are required to determine if this chemokine could be utilized in a blood-based biomarker panel for the diagnosis of lung cancer.

摘要

尽管治疗方法有所进步,但在过去几十年里,肺癌一直是美国癌症相关死亡的主要原因。国家肺癌筛查试验的最新研究结果显示,对高危个体进行低剂量螺旋计算机断层扫描(CT)筛查可降低肺癌死亡率。这表明早期检测对于改善患者预后至关重要。然而,在接受CT扫描的人群中,25%的扫描结果呈阳性,需要进一步的后续研究,这些研究通常涉及更多的辐射暴露和侵入性检查,以减少假阳性结果。本研究的目的是确定候选血浆生物标志物,以帮助诊断高危个体的肺癌。我们发现,与高危对照受试者相比,肺癌患者血浆样本中CXC趋化因子结缔组织激活肽(CTAP)-III的表达增加。通过添加识别CTAP-III和NAP-2的抗NAP-2抗体,证实了该肽的鉴定。我们还通过酶联免疫吸附测定(ELISA)定量并验证了肺癌患者血浆CTAP-III水平(平均值±标准差,1859±1219 ng/mL)高于对照组(698±434 ng/mL;P<0.001)。我们的研究结果表明,肺癌患者血浆中CTAP-III水平升高。需要进一步研究以确定这种趋化因子是否可用于基于血液的生物标志物组合来诊断肺癌。