Suppr超能文献

血管结合蛋白 delta-like 4 及其在乳腺癌中炎症标志物的表达。

Expression of vascular notch ligand delta-like 4 and inflammatory markers in breast cancer.

机构信息

Nuffield Department of Clinical Laboratory Sciences,Weatherall Institute ofMolecular Medicine, University of Oxford, Oxford, UK.

出版信息

Am J Pathol. 2010 Apr;176(4):2019-28. doi: 10.2353/ajpath.2010.090908. Epub 2010 Feb 18.

Abstract

Delta-like ligand 4 (Dll4) is a Notch ligand that is predominantly expressed in the endothelium. Evidence from xenografts suggests that inhibiting Dll4 may overcome resistance to antivascular endothelial growth factor therapy. The aims of this study were to characterize the expression of Dll4 in breast cancer and assess whether it is associated with inflammatory markers and prognosis. We examined 296 breast adenocarcinomas and 38 ductal carcinoma in situ tissues that were represented in tissue microarrays. Additional whole sections representing 10 breast adenocarcinomas, 10 normal breast tissues, and 16 angiosarcomas were included. Immunohistochemistry was then performed by using validated antibodies against Dll4, CD68, CD14, Dendritic Cell-Specific Intercellular adhesion molecule-3-Grabbing Non-integrin (DC-SIGN), CD123, neutrophil elastase, CD31, and carbonic anhydrase 9. Dll4 was selectively expressed by intratumoral endothelial cells in 73% to 100% of breast adenocarcinomas, 18% of in situ ductal carcinomas, and all lactating breast cases, but not normal nonlactating breast. High intensity of endothelial Dll4 expression was a statistically significant adverse prognostic factor in univariate (P = 0.002 and P = 0.01) and multivariate analyses (P = 0.03 and P = 0.04) of overall survival and relapse-free survival, respectively. Among the inflammatory markers, only CD68 and DC-SIGN were significant prognostic factors in univariate (but not multivariate) analyses of overall survival (P = 0.01 and 0.002, respectively). In summary, Dll4 was expressed by endothelium associated with breast cancer cells. In these retrospective subset analyses, endothelial Dll4 expression was a statistically significant multivariate prognostic factor.

摘要

Delta-like 配体 4(Dll4)是一种主要在血管内皮细胞中表达的 Notch 配体。来自异种移植物的证据表明,抑制 Dll4 可能克服对血管内皮生长因子治疗的耐药性。本研究的目的是研究 Dll4 在乳腺癌中的表达特征,并评估其是否与炎症标志物和预后相关。我们检查了 296 例乳腺腺癌和 38 例导管原位癌组织,这些组织代表在组织微阵列中。还包括另外 10 例乳腺腺癌、10 例正常乳腺组织和 16 例血管肉瘤的全切片。然后使用针对 Dll4、CD68、CD14、树突状细胞特异性细胞间黏附分子-3 抓取非整联蛋白(DC-SIGN)、CD123、中性粒细胞弹性蛋白酶、CD31 和碳酸酐酶 9 的验证抗体进行免疫组织化学染色。Dll4 在 73%至 100%的乳腺腺癌、18%的原位导管癌和所有哺乳期乳腺癌中选择性地表达于肿瘤内的内皮细胞,但在正常非哺乳期乳腺中不表达。内皮 Dll4 表达强度高是单因素(P = 0.002 和 P = 0.01)和多因素分析(P = 0.03 和 P = 0.04)中总生存和无复发生存的统计学显著不良预后因素。在炎症标志物中,只有 CD68 和 DC-SIGN 是总生存的单因素(但不是多因素)分析中的显著预后因素(分别为 P = 0.01 和 0.002)。总之,Dll4 由与乳腺癌细胞相关的内皮细胞表达。在这些回顾性亚组分析中,内皮 Dll4 表达是统计学上显著的多因素预后因素。

相似文献

1
Expression of vascular notch ligand delta-like 4 and inflammatory markers in breast cancer.
Am J Pathol. 2010 Apr;176(4):2019-28. doi: 10.2353/ajpath.2010.090908. Epub 2010 Feb 18.
2
Expression of delta-like ligand 4 (Dll4) and markers of hypoxia in colon cancer.
Br J Cancer. 2009 Nov 17;101(10):1749-57. doi: 10.1038/sj.bjc.6605368. Epub 2009 Oct 20.
3
Expression of vascular Notch ligands Delta-like 4 and Jagged-1 in glioblastoma.
Histopathology. 2012 Apr;60(5):740-7. doi: 10.1111/j.1365-2559.2011.04138.x. Epub 2012 Feb 1.
4
Endothelial Delta-like 4 (DLL4) promotes renal cell carcinoma hematogenous metastasis.
Oncotarget. 2014 May 30;5(10):3066-75. doi: 10.18632/oncotarget.1827.
5
Elevated DLL4 expression is correlated with VEGF and predicts poor prognosis of nasopharyngeal carcinoma.
Med Oncol. 2013 Mar;30(1):390. doi: 10.1007/s12032-012-0390-x. Epub 2012 Dec 30.
8
Up-regulation of endothelial delta-like 4 expression correlates with vessel maturation in bladder cancer.
Clin Cancer Res. 2006 Aug 15;12(16):4836-44. doi: 10.1158/1078-0432.CCR-06-0285.
10
Up-regulation of the Notch ligand Delta-like 4 inhibits VEGF-induced endothelial cell function.
Blood. 2006 Feb 1;107(3):931-9. doi: 10.1182/blood-2005-03-1000. Epub 2005 Oct 11.

引用本文的文献

2
Notch signaling regulates pulmonary fibrosis.
Front Cell Dev Biol. 2024 Oct 10;12:1450038. doi: 10.3389/fcell.2024.1450038. eCollection 2024.
3
Population pharmacokinetic model of ABL001/CTX-009 (anti-VEGF/DLL4) in adult cancer patients with solid tumor.
Cancer Sci. 2024 Dec;115(12):3943-3951. doi: 10.1111/cas.16363. Epub 2024 Oct 7.
4
The Prediction of DLL4 as a Prognostic Biomarker in Patients with Gastric Cancer Using Anti-DLL4 Nanobody.
J Gastrointest Cancer. 2024 Sep;55(3):1380-1387. doi: 10.1007/s12029-024-01093-9. Epub 2024 Jul 24.
5
Polyethylenimine Triggers Dll4 Degradation to Regulate Angiogenesis In Vitro.
ACS Omega. 2024 Feb 7;9(7):7502-7510. doi: 10.1021/acsomega.3c06050. eCollection 2024 Feb 20.
7
Tryptanthrin inhibits tumor angiogenesis via Notch/Dll4 signaling pathway in zebrafish.
Transl Cancer Res. 2023 Oct 31;12(10):2660-2672. doi: 10.21037/tcr-23-925. Epub 2023 Oct 16.
9
Carbonic anhydrase IX-related tumoral hypoxia predicts worse prognosis in breast cancer: A systematic review and meta-analysis.
Front Med (Lausanne). 2023 Mar 17;10:1087270. doi: 10.3389/fmed.2023.1087270. eCollection 2023.
10
Targeting adipocyte-immune cell crosstalk to control breast cancer progression.
J Cancer Res Clin Oncol. 2023 Aug;149(10):7969-7979. doi: 10.1007/s00432-023-04685-3. Epub 2023 Mar 13.

本文引用的文献

1
Expression of delta-like ligand 4 (Dll4) and markers of hypoxia in colon cancer.
Br J Cancer. 2009 Nov 17;101(10):1749-57. doi: 10.1038/sj.bjc.6605368. Epub 2009 Oct 20.
2
DLL4 blockade inhibits tumor growth and reduces tumor-initiating cell frequency.
Cell Stem Cell. 2009 Aug 7;5(2):168-77. doi: 10.1016/j.stem.2009.05.019.
3
G-CSF-initiated myeloid cell mobilization and angiogenesis mediate tumor refractoriness to anti-VEGF therapy in mouse models.
Proc Natl Acad Sci U S A. 2009 Apr 21;106(16):6742-7. doi: 10.1073/pnas.0902280106. Epub 2009 Apr 3.
4
Crosstalk of VEGF and Notch pathways in tumour angiogenesis: therapeutic implications.
Front Biosci (Landmark Ed). 2009 Jan 1;14(8):3094-110. doi: 10.2741/3438.
5
Cross-talk between tumor and endothelial cells involving the Notch3-Dll4 interaction marks escape from tumor dormancy.
Cancer Res. 2009 Feb 15;69(4):1314-23. doi: 10.1158/0008-5472.CAN-08-2791. Epub 2009 Feb 10.
10
Paclitaxel plus bevacizumab versus paclitaxel alone for metastatic breast cancer.
N Engl J Med. 2007 Dec 27;357(26):2666-76. doi: 10.1056/NEJMoa072113.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验