The DOI matches its Crossref record; 110 of the 110 references it cites were found in a registry or an index.
Tumorigenesis and the angiogenic switch
Abstract
It has become evident that we cannot understand tumour growth without considering components of the stromal microenvironment, such as the vasculature. At the same time, the tumour phenotype determines the nature of the tumour vasculature. Much research is now devoted to determining the impact of angiogenesis on tumour development and progression, and the reciprocal influences of tumour products on the microvasculature. A more detailed understanding of the complex parameters that govern the interactions between the tumour and vascular compartments will help to improve anti-angiogenic strategies-- not only for cancer treatment, but also for preventing recurrence.
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“This neovascularization represents a rate-limiting step in tumor progression [47].”
From Modeling Tumor Microenvironment Complexity In Vitro: Spheroids as Physiologically Relevant Tumor Models and Strategies for Their Analysis (2025) · cites this paper as [47]
In the citing paper
“Instead of triggering angiogenesis, some tumors co-opt existing vasculature and grow along the vessels [53][54][55][56], until the demand for nutrients and oxygen becomes too large and angiogenesis starts again [53,55].”
From Cancer-on-chip models for metastasis: importance of the tumor microenvironment (2024) · cites this paper as [55]
Citations
Cites
1 retracted
Watnick, R. S., Cheng, Y.-N., Rangarajan, A., Ince, T. A., & Weinberg, R. A. (2003) · Cancer Cell · doi:10.1016/s1535-6108(03)00030-8 · Cited by 318
RetractedHanahan, D., & Weinberg, R. A. (2000) · Cell · doi:10.1016/s0092-8674(00)81683-9 · Cited by 29,219
Patterns and emerging mechanisms of the angiogenic switch during tumorigenesis
Hanahan, D., & Folkman, J. (1996) · Cell · doi:10.1016/s0092-8674(00)80108-7 · Cited by 6,885
Genetic Alterations during Colorectal-Tumor Development
Vogelstein, B., Fearon, E. R., Hamilton, S. R., Kern, S. E., Preisinger, A. C., Leppert, M., de Vries-Smits, A. M. M., & Bos, J. L. (1988) · New England Journal of Medicine · doi:10.1056/nejm198809013190901 · Cited by 6,704
Vascular endothelial growth factor induced by hypoxia may mediate hypoxia-initiated angiogenesis
Shweiki, D., Itin, A., Soffer, D., & Keshet, E. (1992) · Nature · doi:10.1038/359843a0 · Cited by 4,617
Endostatin: an endogenous inhibitor of angiogenesis and tumor growth
O'Reilly, M. S., Boehm, T., Shing, Y., Fukai, N., Vasios, G., Lane, W. S., Flynn, E., Birkhead, J. R., Olsen, B. R., & Folkman, J. (1997) · Cell · doi:10.1016/s0092-8674(00)81848-6 · Cited by 4,486
Tumors: Wounds That Do Not Heal
Flier, J. S., Underhill, L. H., & Dvorak, H. F. (1986) · New England Journal of Medicine · doi:10.1056/nejm198612253152606 · Cited by 4,391
Mechanisms of angiogenesis and arteriogenesis
Carmeliet, P. (2000) · Nature Medicine · doi:10.1038/74651 · Cited by 4,235
Activation of vascular endothelial growth factor gene transcription by hypoxia-inducible factor 1
Forsythe, J. A., Jiang, B.-H., Iyer, N. V., Agani, F., Leung, S. W., Koos, R. D., & Semenza, G. L. (1996) · Molecular and Cellular Biology · doi:10.1128/mcb.16.9.4604 · Cited by 3,981
Vascular-specific growth factors and blood vessel formation
Yancopoulos, G. D., Davis, S., Gale, N. W., Rudge, J. S., Wiegand, S. J., & Holash, J. (2000) · Nature · doi:10.1038/35025215 · Cited by 3,699
Research works printed but not linked: 2
- Folkman, J. in Cancer Medicine (Holland, M.D. et al.) 2546 (BC Decker, Hamilton, Ontario, 2000).
- Sternlicht, M. D. et al. Matrix proteinases as emerging targets in anticancer therapy: status and prospects. ETT 4, 609–633 (2000).
Cited by
Sorted by citations
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Toffoli, S., Féron, O., Raes, M. J., & Michiels, C. (2007) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2007.06.002 · Cited by 69
Белоусова, Е. Л., Karmazanovsky, G. G., Kriger, A. G., Kalinin, D. V., Mannelli, L., Glotov, A. V., Karelskaya, N. A., Paklina, O. V., & Kaldarov, A. R. (2016) · Clinical Radiology · doi:10.1016/j.crad.2016.10.021 · Cited by 65
Dzobo, K., & Dandara, C. (2020) · OMICS A Journal of Integrative Biology · doi:10.1089/omi.2020.0023 · Cited by 65
“Migration and invasion of tumor cells into the surrounding tissues induce angiogenesis as well (Bergers and Benjamin, 2003).”
Guo, L., Wang, Z., Du, Y., Mao, J., Zhang, J., Yu, Z., Guo, J., Zhao, J., Zhou, H., Wang, H., et al. (2020) · Cancer Cell International · doi:10.1186/s12935-020-01274-z · Cited by 67
β-Caryophyllene Induces Apoptosis and Inhibits Angiogenesis in Colorectal Cancer Models
Dahham, S. S., Tabana, Y., Asif, M., Ahmed, M., Babu, D., Hassan, L. E. A., Ahamed, M. B. K., Sandai, D. A., Barakat, K., Siraki, A. G., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms221910550 · Cited by 65
Hypoxia upregulates expression of human endosialin gene via hypoxia-inducible factor 2
Ohradanova‐Repic, A., Gradin, K., Baráthová, M., Zaťovičová, M., Holotnakova, T., Kopáček, J., Parkkila, S., Poellinger, L., Pastoreková, S., & Pastorek, J. (2008) · British Journal of Cancer · doi:10.1038/sj.bjc.6604685 · Cited by 65
Ojha, R., Jha, V., Singh, S. K., & Bhattacharyya, S. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2014.07.007 · Cited by 68
Angiogenesis inhibitors in the treatment of prostate cancer
Hwang, C., & Heath, E. I. (2010) · Journal of Hematology & Oncology · doi:10.1186/1756-8722-3-26 · Cited by 67
Role of hypoxia and vascular endothelial growth factors in lymphangiogenesis
Morfoisse, F., Renaud-Gabardos, E., Hantelys, F., Prats, A., & Garmy-Susini, B. H. (2014) · Molecular & Cellular Oncology · doi:10.4161/mco.29907 · Cited by 68
Drug delivery strategies for therapeutic angiogenesis and antiangiogenesis
Bhise, N. S., Shmueli, R. B., Sunshine, J. C., Tzeng, S. Y., & Green, J. J. (2011) · Expert Opinion on Drug Delivery · doi:10.1517/17425247.2011.558082 · Cited by 65
Zhao, C., Yang, H., Shi, H., Wang, X., Chen, X., Yuan, Y., Lin, S., & Wei, Y. (2011) · Carcinogenesis · doi:10.1093/carcin/bgr076 · Cited by 65
Eikesdal, H. P., Sugimoto, H., Birrane, G., Maeshima, Y., Cooke, V. G., Kieran, M. W., & Kalluri, R. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0807055105 · Cited by 68
Angiopoietin-4 Promotes Glioblastoma Progression by Enhancing Tumor Cell Viability and Angiogenesis
Brunckhorst, M. K., Wang, H., Lu, R., & Yu, Q. (2010) · Cancer Research · doi:10.1158/0008-5472.can-09-4125 · Cited by 66
Mesoporous Silica Nanoparticles as an Antitumoral-Angiogenesis Strategy
Setyawati, M. I., & Leong, D. T. (2017) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.6b12524 · Cited by 65
AKIP1 promotes angiogenesis and tumor growth by upregulating CXC-chemokines in cervical cancer cells
Zhang, W., Wu, Q., Wang, C., Yang, L., Liu, P., & Ma, C. (2018) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-018-3335-7 · Cited by 65
Marques, J. H. D. M., Mota, A. L., de Oliveira, J. G., Lacerda, J. Z., Stefani, J. P., Ferreira, L. C., de Castro, T. B., Aristizábal-Pachón, A. F., & Zuccari, D. A. P. D. C. (2018) · Life Sciences · doi:10.1016/j.lfs.2018.07.012 · Cited by 65
Targeting endothelial metabolism for anti-angiogenesis therapy: A pharmacological perspective
Missiaen, R., Morales-Rodriguez, F., Eelen, G., & Carmeliet, P. (2017) · Vascular Pharmacology · doi:10.1016/j.vph.2017.01.001 · Cited by 58
Son, H., Nam, J.-O., Kim, S., & Kim, I.-S. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.06.012 · Cited by 61
Yoshiji, H., Noguchi, R., Kitade, M., Kaji, K., Ikenaka, Y., Namisaki, T., Yoshii, J., Yanase, K., Yamazaki, M., Tsujimoto, T., et al. (2009) · Journal of Gastroenterology · doi:10.1007/s00535-009-0031-0 · Cited by 64
Müller, M. J., Gerndt, S., Chao, Y., Zisis, T., Nguyen, O. N. P., Gerwien, A., Urban, N. D., Müller, C., Gegenfurtner, F. A., Geisslinger, F., et al. (2021) · Cell chemical biology · doi:10.1016/j.chembiol.2021.01.023 · Cited by 66
Targeting Tumor-Stromal Interactions in Pancreatic Cancer: Impact of Collagens and Mechanical Traits
Maneshi, P., Mason, J. E., Dongre, M., & Öhlund, D. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.787485 · Cited by 68
Angiogenesis: From Chronic Liver Inflammation to Hepatocellular Carcinoma
Sanz-Cameno, P., Trapero-Marugán, M., Chaparro, M., Jones, E. A., & Moreno‐Otero, R. (2010) · Journal of Oncology · doi:10.1155/2010/272170 · Cited by 64
Brain Metastases: Epidemiology and Pathophysiology
Sul, J., & Posner, J. B. (2007) · Cancer treatment and research · doi:10.1007/978-0-387-69222-7_1 · Cited by 65
Metronomic chemotherapy: an antiangiogenic scheduling
Laquente, B., Viñals, F., & Germà, J. R. (2007) · Clinical & Translational Oncology · doi:10.1007/s12094-007-0018-3 · Cited by 64
Li, Z., Zhang, H., Chen, Y., Li, F., & Fang, J. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.291708 · Cited by 66
Phosphorylation of αB-crystallin: Role in stress, aging and patho-physiological conditions
Raman, B., Akula, K. K., Ramakrishna, T., & Rao, C. M. (2015) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2015.09.017 · Cited by 64
Cancer-Associated Intermediate Conductance Ca2+-Activated K+ Channel KCa3.1
Mohr, C. J., Steudel, F. A., Gross, D., Ruth, P., Lo, W., Hoppe, R., Schroth, W., Brauch, H. B., Huber, S. M., & Łukowski, R. (2019) · Cancers · doi:10.3390/cancers11010109 · Cited by 64
Tumor progression-dependent angiogenesis in gastric cancer and its potential application
Hsieh, H., & Tsai, M.-M. (2019) · World Journal of Gastrointestinal Oncology · doi:10.4251/wjgo.v11.i9.686 · Cited by 66
The Potential of Antiangiogenic Therapy in Non–Small Cell Lung Cancer
Giaccone, G. (2007) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-06-2186 · Cited by 64
Hou, J., Cao, J., Gao, L., Zhang, F., Shen, J., Zhou, L., Shi, J., Feng, Y., Yan, Z., Wang, D., et al. (2021) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2021.09.027 · Cited by 63
Do, M. H., Shi, W., Ji, L., Ladewig, E., Zhang, X., Srivastava, R. M., Capistrano, K. J., Edwards, C., Malik, I., Nixon, B. G., et al. (2023) · Immunity · doi:10.1016/j.immuni.2023.10.010 · Cited by 64
Model-based angiogenic inhibition of tumor growth using modern robust control method
Kovács, L., Szeles, A., Sápi, J., Drexler, D. A., Rudas, I. J., Harmati, I., & Sápi, Z. (2014) · Computer Methods and Programs in Biomedicine · doi:10.1016/j.cmpb.2014.01.002 · Cited by 63
“[30] G.”
BackgroundThe Kunitz-Like Modulatory Protein Haemangin Is Vital for Hard Tick Blood-Feeding Success
Islam, M. K., Tsuji, N., Miyoshi, T., Alim, M. A., Huang, X., Hatta, T., & Fujisaki, K. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000497 · Cited by 63
Multiscale Imaging and Computational Modeling of Blood Flow in the Tumor Vasculature
Kim, E., Stamatelos, S. K., Cebulla, J., Bhujwalla, Z. M., Popel, A. S., & Pathak, A. P. (2012) · Annals of Biomedical Engineering · doi:10.1007/s10439-012-0585-5 · Cited by 63
Dango, S., Sienel, W. G. R., Schreiber, M., Stremmel, C., Kirschbaum, A., Pantel, K., & Passlick, B. (2008) · Lung Cancer · doi:10.1016/j.lungcan.2007.11.015 · Cited by 63
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Gallach, S., Fariñas, S. C., Lewintre, E. J., & Camps, C. (2014) · BioMed Research International · doi:10.1155/2014/878450 · Cited by 64
Ali, R., Toh, H.-C., Chia, W.-K. J., & The ASCOLT trial investigators (2011) · Trials · doi:10.1186/1745-6215-12-261 · Cited by 64
Multimodality Tumor Imaging Targeting Integrin α v β 3
Cai, W., Gambhir, S. S., & Chen, X. S. (2005) · BioTechniques · doi:10.2144/000112091 · Cited by 63
Chuang, J., Chen, P., Tsao, C.-W., Chang, A., Lein, M., Lin, C.-C., Wang, S., Lin, C., & Tang, C. (2015) · Oncotarget · doi:10.18632/oncotarget.2978 · Cited by 62
Adipocytes: active facilitators in epithelial ovarian cancer progression?
Dai, L., Song, K., & Di, W. J. (2020) · Journal of Ovarian Research · doi:10.1186/s13048-020-00718-4 · Cited by 63
Molecular Pathogenesis of Glioblastoma in Adults and Future Perspectives: A Systematic Review
Esemen, Y., Awan, M., Parwez, R., Baig, A., Rahman, S., Masala, I., Franchini, S., & Giakoumettis, D. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052607 · Cited by 64
3D microengineered vascularized tumor spheroids for drug delivery and efficacy testing
Ahn, J., Kim, D., Koo, D.-J., Lim, J., Park, T., Lee, J., Ko, J., Kim, S., Kim, M., Kang, K., et al. (2022) · Acta Biomaterialia · doi:10.1016/j.actbio.2022.10.009 · Cited by 64
CXCR4 and CXCR7 regulate angiogenesis and CT26.WT tumor growth independent from SDF‐1
Kollmar, O., Rupertus, K., Scheuer, C., Nickels, R. M., Haberl, G. C. Y., Tilton, B., Menger, M. D., & Schilling, M. K. (2009) · International Journal of Cancer · doi:10.1002/ijc.24956 · Cited by 62
Pollina, E. A., Legesse-Miller, A., Haley, E. M., Goodpaster, T. A., Randolph‐Habecker, J., & Coller, H. A. (2008) · Cell Cycle · doi:10.4161/cc.7.13.6240 · Cited by 61
Angiogenesis and Anti-Angiogenic Molecularly Targeted Therapies in Malignant Gliomas
Argyriou, A. A., Giannopoulou, E., & Kalofonos, H. P. (2009) · Oncology · doi:10.1159/000218165 · Cited by 61
Inhibition of angiogenesis and invasion in malignant gliomas
Chi, A. S., Norden, A. D., & Wen, P. Y. (2007) · Expert Review of Anticancer Therapy · doi:10.1586/14737140.7.11.1537 · Cited by 63
Contrast enhancement pattern on multidetector CT predicts malignancy in pancreatic endocrine tumours
Cappelli, C., Boggi, U., Mazzeo, S., Cervelli, R., Campani, D., Funel, N., Contillo, B. P., & Bartolozzi, C. (2014) · European Radiology · doi:10.1007/s00330-014-3485-2 · Cited by 62
Kamstock, D. A., Guth, A., Elmslie, R. E., Kurzman, I. D., Liggitt, D., Coro, L., Fairman, J., & DOW, S. W. (2005) · Cancer Gene Therapy · doi:10.1038/sj.cgt.7700895 · Cited by 62
Vascular Endothelial Growth Factor and Vascular Homeostasis
Lazarus, A., & Keshet, E. (2011) · Proceedings of the American Thoracic Society · doi:10.1513/pats.201102-021mw · Cited by 64
Anti-angiogenic gene therapy in the treatment of malignant gliomas
Gatson, N. T., Chiocca, E. A., & Kaur, B. (2012) · Neuroscience Letters · doi:10.1016/j.neulet.2012.08.001 · Cited by 62
Chen, W., Mao, K., Liu, Z., & Dinh‐Xuan, A. T. (2014) · Oncology Letters · doi:10.3892/ol.2014.2471 · Cited by 61
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Simone, V. D., Brunetti, O., Lupo, L., Testini, M., Maiorano, E., Simone, M. D., Longo, V., Rolfo, C. D., Peeters, M., Scarpa, A., et al. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18020418 · Cited by 61
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Castet, F., García‐Mulero, S., Pamplona, R. S., Cuellar, A., Casanovas, O., Mitjana, J. M. C., & Piulats, J. M. (2019) · Cancers · doi:10.3390/cancers11060834 · Cited by 64
Sun, L., Luo, J., Mackey, L. V., Fuselier, J. A., & Coy, D. H. (2006) · Cancer Letters · doi:10.1016/j.canlet.2006.02.016 · Cited by 62
Irinotecan therapy and molecular targets in colorectal cancer: A systemic review
Weekes, J., Lam, A. K.-Y., Sebesan, S., & Ho, Y. (2009) · World Journal of Gastroenterology · doi:10.3748/wjg.15.3597 · Cited by 62
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Velliou, R.-I., Legaki, A., Nikolakopoulou, P., Vlachogiannis, N. I., & Chatzigeorgiou, A. (2023) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-04966-7 · Cited by 64
“Angiogenesis is essential for a variety of cellular processes, growth and spread of tumour cells [159].”
BackgroundMicroenvironment Changes (in pH) Affect VEGF Alternative Splicing
Elias, A. P., & Dias, S. (2008) · Cancer Microenvironment · doi:10.1007/s12307-008-0013-4 · Cited by 64
TWEAK and Fn14: New molecular targets for cancer therapy?
Winkles, J. A., Tran, N. L., & Berens, M. E. (2005) · Cancer Letters · doi:10.1016/j.canlet.2005.03.048 · Cited by 61
Imaging aspects of the tumor stroma with therapeutic implications
Narunsky-Haziza, L., Oren, R., Bochner, F., & Neeman, M. (2013) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2013.10.003 · Cited by 59
Vicari, D., Foy, K. C., Liotta, E. M., & Kaumaya, P. T. P. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.216812 · Cited by 61
Romagnoli, R., Baraldi, P. G., Salvador, M. K., Prencipe, F., Bertolasi, V., Cancellieri, M., Brancale, A., Hamel, E., Castagliuolo, I., Consolaro, F., et al. (2014) · Journal of Medicinal Chemistry · doi:10.1021/jm5008193 · Cited by 61
Liang, W. P., Kujawski, M., Wu, J., Lu, J., Herrmann, A., Loera, S., Yen, Y., Lee, F., Yu, H., Wen, W. X., et al. (2010) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-09-1486 · Cited by 61
Chandru, H. K., Sharada, A. C., Bettadaiah, B. K., Kumar, C. S. A., Rangappa, K. S., Sunila, & Jayashree, K. (2007) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2007.08.051 · Cited by 61
van Horssen, R., Galjart, N., Rens, J. A. P., Eggermont, A. M. M., & ten Hagen, T. L. M. (2006) · Journal of Cellular Biochemistry · doi:10.1002/jcb.20994 · Cited by 61
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Rajabi, S., Dehghan, M. H., Dastmalchi, R., Mashayekhi, F. J., Salami, S., & Hedayati, M. (2019) · Endocrine Journal · doi:10.1507/endocrj.ej18-0537 · Cited by 63
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Pickup, M. W., Owens, P., & Moses, H. L. (2017) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a022285 · Cited by 63
Lee, J., Kim, S.-E., Moon, D., & Doh, J. (2021) · Lab on a Chip · doi:10.1039/d1lc00182e · Cited by 59
Lee, H., Xue, J., Chou, P., Zhou, A., Yang, P., Conrad, C. A., Aldape, K., Priebe, W., Patterson, C., Sawaya, R. A., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.3540 · Cited by 64
Bottos, A., Martini, M., Nicolantonio, F. D., Comunanza, V., Maione, F., Minassi, A., Appendino, G., Bussolino, F., & Bardelli, A. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1105026109 · Cited by 61
Pharmacokinetics and excretion of 14C-lenvatinib in patients with advanced solid tumors or lymphomas
Dubbelman, A.-C., Rosing, H., Nijenhuis, C. M., Huitema, A. D. R., Mergui‐Roelvink, M., Gupta, A., Verbel, D., Thompson, G. A., Shumaker, R., Schellens, J. H. M., et al. (2014) · Investigational New Drugs · doi:10.1007/s10637-014-0181-7 · Cited by 60
Liu, Z., Jia, B., Shi, J., Jin, X., Zhao, H., Li, F., Liu, S., & Wang, F. (2010) · Bioconjugate Chemistry · doi:10.1021/bc900547d · Cited by 60
Macrophage Migration Inhibitory Factor: a Potential Marker for Cancer Diagnosis and Therapy
Babu, S. N., Chetal, G., & Kumar, S. (2012) · Asian Pacific Journal of Cancer Prevention · doi:10.7314/apjcp.2012.13.5.1737 · Cited by 60
Marty, M. E., & Pivot, X. B. (2008) · European Journal of Cancer · doi:10.1016/j.ejca.2008.01.005 · Cited by 60
Naumova, E., Ubezio, P., Garofalo, A., Borsotti, P., Cassis, L., Riccardi, E., Scanziani, E., Eccles, S. A., Bani, M. R., & Giavazzi, R. (2006) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-05-1615 · Cited by 60
Notch Regulation of Tumor Angiogenesis
Bridges, E., Oon, C. E., & Harris, A. L. (2011) · Future Oncology · doi:10.2217/fon.11.20 · Cited by 60
Brantley‐Sieders, D. M., Dunaway, C. M., Rao, M., Short, S. P., Hwang, Y., Gao, Y., Li, D., Jiang, A., Shyr, Y., Wu, J. Y., et al. (2010) · Cancer Research · doi:10.1158/0008-5472.can-10-3396 · Cited by 60
Tumor growth or regression: powered by inflammation
Nelson, D. J., & Ganß, R. (2006) · Journal of Leukocyte Biology · doi:10.1189/jlb.1105646 · Cited by 60
Wille, C., Köhler, C., Armacki, M., Jamali, A., Gößele, U., Pfizenmaier, K., Seufferlein, T. T. W., & Eiseler, T. (2013) · Molecular Biology of the Cell · doi:10.1091/mbc.e13-06-0334 · Cited by 60
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Yang, L., Zhang, Y., Yao, Z., Li, S., Yin, Z., & Xu, M. (2016) · International Journal of Oncology · doi:10.3892/ijo.2016.3517 · Cited by 59
Casey, L., & Singh, N. (2019) · Histopathology · doi:10.1111/his.13985 · Cited by 60
Daum, S., Hagen, H., Naismith, E., Wolf, D. G. F., & Pircher, A. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.610903 · Cited by 60
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Asosingh, K., Raeve, H. D., Menu, E., Riet, I. V., Marck, E. V., Camp, B. V., & Vanderkerken, K. (2003) · Blood · doi:10.1182/blood-2003-08-2946 · Cited by 60
Zhang, C.-Z. (2017) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2017.05.155 · Cited by 59
Klemba, A., Bodnar, L., Waś, H., Brodaczewska, K. K., Wcisło, G., Szczylik, C. A., & Kiéda, C. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249492 · Cited by 59
Carbon Ions for Hypoxic Tumors: Are We Making the Most of Them?
Sokol, O., & Durante, M. (2023) · Cancers · doi:10.3390/cancers15184494 · Cited by 58
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Lamplugh, Z. L., Wellhausen, N., June, C. H., & Fan, Y. (2025) · Nature reviews. Immunology · doi:10.1038/s41577-025-01229-3 · Cited by 76
“vasculature and into the tumour by overexpressing vascular endothelial growth factor (VEGF) and other molecules, thereby inducing the downregulation of adhesion molecules that are required for leukocyte extravasation, including intercellular adhesion molecule 1 (ICAM1) and vascular cell adhesion molecule 1 (VCAM1) 6–9…”
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Bizama, C., García, P., Espinoza, J. A., Weber, H. L., Leal, P., Nervi, B., & Roa, J. C. (2015) · Cancer Treatment Reviews · doi:10.1016/j.ctrv.2015.01.003 · Cited by 59
Huang, S., Yang, N., Liu, Y., Gao, J., Huang, T., Hu, L., Zhao, J., Li, Y., Li, C., & Zhang, X. (2012) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2012.1147 · Cited by 61
Banerjee, S., Mehta, S., Haque, I., Sengupta, K., Dhar, K., Kambhampati, S., Veldhuizen, P. J. V., & Banerjee, S. K. (2008) · Biochemistry · doi:10.1021/bi8000352 · Cited by 59
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Sheehan, K. M., Gulmann, C., Eichler, G. S., Weinstein, J. N., Barrett, H. L., Kay, E. W., Conroy, R. M., Liotta, L. A., & Petricoin, E. F. (2007) · Oncogene · doi:10.1038/sj.onc.1210647 · Cited by 59
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Roodink, I., & Leenders, W. P. J. (2010) · Cancer Letters · doi:10.1016/j.canlet.2010.09.004 · Cited by 57
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Wang, Z., Yang, P., Xu, H., Qian, A., Hu, L., & Shang, P. (2009) · Bioelectromagnetics · doi:10.1002/bem.20501 · Cited by 59
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Kim, M., Lee, C., Payne, R. M., Yue, B. Y. J. T., Chang, J.-H., & Ying, H. (2015) · Survey of Ophthalmology · doi:10.1016/j.survophthal.2015.04.003 · Cited by 60
Sengupta, K., Banerjee, S., Saxena, N. K., & Banerjee, S. K. (2004) · Molecular Cancer Research · doi:10.1158/1541-7786.150.2.3 · Cited by 59
Verry, C., Dufort, S., Barbier, E., Montigon, O., Péoc’h, M., Chartier, P., Lux, F., Balosso, J., Tillement, O., Sancey, L., et al. (2016) · Nanomedicine · doi:10.2217/nnm-2016-0203 · Cited by 59
Takano, M., Shimada, K., Fujii, T., Morita, K., Takeda, M., Nakajima, Y., Nonomura, A., Konishi, N., & Obayashi, C. (2016) · BMC Cancer · doi:10.1186/s12885-016-2949-y · Cited by 59
Metadata
- Authors
- Bergers, G., & Benjamin, L. E.
- Affiliations
- University of California, San Francisco (US)
- Beth Israel Deaconess Medical Center (US)
- Corresponding author
- Bergers, Gabriele
- ORCID
- Bergers, Gabriele
- Venue
- Nature reviews. Cancer
- Published
- 2003-06
- Volume
- 3
- Issue
- 6
- Pages
- 401-410
- ISSN
- 1474-175X (ISSN-L)
- 1474-1768
- OpenAlex
- W2804842145
- Cited by
- 3,559
- References
- 110
- Citations by year
- 2026: 53 · 2025: 79 · 2024: 123 · 2023: 122 · 2022: 142 · 2021: 160 · 2020: 149 · 2019: 159 · 2018: 162 · 2017: 176 · 2016: 148 · 2015: 176 · 2014: 232 · 2013: 223 · 2012: 198
- FWCI
- 9.49
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Cancer (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
- Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
- Physical Sciences › Mathematics › Modeling and Simulation › Mathematical Biology Tumor Growth
- Keywords
- carcinogenesis, angiogenic switch, tumor angiogenesis, tumor vasculature, tumor microenvironment, tumor-stroma interactions, tumor progression, anti-angiogenic therapy, tumor recurrence
- MeSH terms
- Animals, Humans, Neoplasms, Neovascularization, Pathologic, Disease Progression
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