个人信息
Personal Information
联系方式
Contact Information
个人简介
Personal Profile
瑞典卡罗林斯卡医学院微生物和肿瘤生物学系教授,丹麦哥本哈根大学荣誉教授,欧洲科学院院士,欧洲科学与艺术学院院士,美国发明家学院院士,中国工程院外籍院士。1978年考入山东医学院。1983-1986年,在中国医学科学院血液学研究所工作,主要从事筛选人白细胞表面抗原相关的单克隆抗体研究。1993年获得瑞典卡罗林斯卡医学院博士学位,1993-1996年在美国哈佛医学院儿童医院 Folkman’s 实验室从事博士后研究。1996年回到瑞典卡罗林斯卡医学院工作至今,并于2004 年获卡罗林斯卡医学院终生教授。至今,在血管生成领域做出了大量突破性研究贡献,包括血管生成在病理生理条件下的信号分子传导,针对癌症,肥胖和心血管等疾病的新型靶向治疗方法,研究成果处于国际领先地位,受到众多欧洲研究委员会和NOVO-Nordisk基金会的优先资助,并开创了用通过靶向抑制血管新生来治疗代谢性疾病的新领域。当前的研究领域主要包括肥胖、代谢性疾病、糖尿病并发症、肿瘤及转移、心血管疾病等疾病的病理性血管新生的机制的研究,其中,在脂肪组织中的血管生成研究领域位居世界前沿,近期又开展了血管与造血以及肿瘤造血等造血相关研究。至今已发表论文220多篇(平均每篇的影响因子大于9.7,H指数为86),获得国际专利60多项,受邀在国际会议发言100多次(包括美国癌症年会,高登研究会议,欧洲血管生成会议等)。是瑞典卡罗林斯卡医学院杰出教授奖和欧洲 ERC 高级研究奖的获得者。
上传附件
支持扩展名:.rar .zip .doc .docx .pdf .jpg .png .jpeg上传附件
支持扩展名:.rar .zip .doc .docx .pdf .jpg .png .jpeg上传附件
支持扩展名:.rar .zip .doc .docx .pdf .jpg .png .jpeg1.血管相关细胞对肿瘤发展的影响及其转化研究。实验血液学国家重点实验室开放课题(启动资金,2019-)。
代表著作38篇(第一作者或通讯作者)
一.特邀专家评述代表著作(10篇)
1. Cao Y. Detrimental effects of anti-VEGF-basedantiangiogenic cancer drugs on endocrinesystem. NatureReview Endocrinology, 2014 Sep;10(9):530-9. doi:
10.1038/nrendo.2014.114.Epub 2014 Jul 22.
2. Cao Y. Multifarious functions of the PDGF system inmodulation of angiogenesis, vascularintegrity, tumor growth and metastasis, Trendsin Molecular Medicine.
Aug;19(8):460-73.2013.
3. Cao YH. Off-tumor target-beneficial site forantiangiogenic cancer therapy? Nature Rev Clin Oncol. 2010;7:604-608
4. Cao Y, Langer R. Optimizing the delivery of cancer drugsthat block angiogenesis. ScienceTransl Med. 2010;2:15ps13
5. Cao Y. Adipose tissue angiogenesis as a therapeutictarget for obesity and metabolic diseases. Nature Rev DrugDiscov. 2010;9:107-115
6. Cao Y. Wake-up call for endothelial cells. Blood.2010;115:2336-2337
7. Cao Y, Langer R. A review of Judah Folkman's remarkableachievements in biomedicine.Proc Natl Acad Sci U S A. 2008;105:13203-13205
8. Cao Y. Angiogenesis modulates adipogenesis and obesity. J Clin Invest.
2007;117:2362-2368
9. Cao YH. VEGF calls its receptors from the recyclingcompartment. Blood.
2006;108:2506-2507
10. Cao Y. Opinion: Emerging mechanisms oftumourlymphangiogenesis and lymphatic metastasis. Nature Rev Cancer. 2005;5:735-743
二.研究论文代表著作(28篇)
1. Adipocyte and Lipid Metabolism in Cancer Drug Resistance. J ClinInvest. 2019 Jul 2;129(8):3006-3017.
2. Bladder drug mirabegron exacerbates atherosclerosisthrough activation of brown fat-mediated lipolysis. ProcNatlAcadSci U S A. 2019May28;116(22):10937-10942.
3. Endothelial lifediscontinues without Erk. J Exp Med. 2019 Aug 5;216(8):1730-1732.
4. Ablation ofendothelial VEGFR1 improves metabolic dysfunction by inducing adipose tissuebrowning. J Exp Med. 2018 Feb 5;215(2):611-626.
5. A Novel Concept of the Smart NIR-Light-Controlled DrugReleaseof Black Phosphorus Nanostructure for Cancer Therapy. ProcNatlAcadSciU S A. 2018 Jan 16;115(3):501-506.
6. Obesity Protects Cancerfrom Drugs Targeting Blood Vessels. Cell Metab. 2018Jun 5;27(6):1163-1165.
7. Cancer Lipid Metabolism Confers Antiangiogenic Drug Resistance. CellMetab.2018 Jul 3;28(1):104-117.e5.
8. Off-tumor targets confer antiangiogenicdrug resistance byinducing erythropoietin production in the host macroenvironment. ProcNatlAcadSciU S A. 2017 Nov 7;114(45):E9635-E9644..
9. A zebrafish model discovers a novelmechanism of stromalfibroblast-mediated cancer metastasis. ClinicalCancer Res. 2017Apr 18. pii: clincanres.0101.2017. doi:10.1158/1078-0432.CCR-17-0101. 2017
10. Discontinuation of anti-VEGF cancer therapy promotesmetastasis through a liverrevascularization mechanism, NatureCommunications, 1;7:12680., 2016
11. Endothelial PDGF-CC MediatesAngiogenesis-DependentThermogenesis in Browning Fat. NatureCommunications,7:12152., 2016
12. The PDGF-BB-SOX7 axis-modulated IL-33 in pericytesandstromal cells promotes metastasis through tumour-associated macrophages. NatureCommunications,2016 May 6;7:11385. doi: 10.1038/ncomms11385.
13. Modulation of age-related insulin sensitivity by VEGF-dependentvascular plasticity inadipose tissues. ProcNatl Acad Sci U S A. 2014 Sep 30. pii: 201415825, 2014
14. TNFR1-mediates TNF-á-induced tumorinflammatorylymphangiogenesis and lymphatic metastasis by orchestrating the VEGF-C-–VEGFR3signaling pathway, Nature Communications, | 5:4944 |DOI:10.1038/ncomms5944 |2014
15. Opposing effectsof anti-PDGF drug-induced metastasis. NatureCommunication. 8;4:2129, 2013.
16. PDGF-B modulates hematopoiesis and tumor angiogenesis byswitchingon hypoxia-independent but ATF3-dependent erythropoietin production instromal cells.Nature Medicine.; Dec 4;18(1):100-10 2011
17. Mouse corneallymphangiogenesis model. Nature Protoc. 2011;Jun;6(6):817-26.
18. Hypoxia-induced retinopathy model in adult zebrafish. Nature Protoc. 2010;5:1903- 1910
19. Angiogenic factors FGF2 and PDGF-BB synergisticallypromote murine tumorneovascularization and metastasis. J Clin Invest. 2007;117:2766-2777
20. Presence of bone marrow- derivedcirculating progenitorendothelial cells in the newly formed lymphatic vessels. Blood.2005;106:4184-4190
21. PDGF-BB induces intratumorallymphangiogenesis andpromotes lymphatic metastasis. Cancer Cell. 2004;6:333-345
22. Angiogenic synergism, vascular stability and improvementof hind-limb ischemia by acombination of PDGF-BB and FGF-2. Nature Med. 2003;9:604-613
23. Placenta growth factor-1 antagonizes VEGF-inducedangiogenesis andtumor growth by the formation of functionally inactivePlGF-1/VEGF heterodimers.Cancer Cell. 2002;1:99-108
24. Cao Y, Cao R.Angiogenesis inhibited by drinking tea. Nature. 1999;398:381
25. Cao Y, O'Reilly MS, Marshall B, Flynn E, Ji RW, FolkmanJ. Expression of angiostatincdna in a murine fibrosarcoma suppresses primarytumor growth and produces long-termdormancy of metastases. J Clin Invest. 1998;101:1055-1063
26. Cao Y, Linden P, Farnebo J, Cao R, Eriksson A, Kumar V,Qi JH, Claesson-Welsh L,Alitalo K. Vascular endothelial growth factor C inducesangiogenesis in vivo. Proc NatlAcad Sci U S A. 1998;95:14389-14394
27. Cao Y, Linden P, Shima D, Browne F, Folkman J. In vivoangiogenic activity and hypoxiainduction of heterodimers of placenta growthfactor/vascular endothelial growth factor. JClin Invest. 1996;98:2507-2511
28. Cao Y, Chen C, Weatherbee JA, Tsang M, Folkman J.Gro-beta, a -c-x-c- chemokine, is anangiogenesis inhibitor that suppresses thegrowth of lewis lung carcinoma in mice. J ExpMed. 1995;182:2069-2077
北京协和医学院研究生院招生办公室
360eol提供技术支持
文件上传中...