Relevant bibliographies by topics / Co-option vasculaire

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Co-option vasculaire'

Author: Grafiati
Published: 22 February 2025

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Journal articles on the topic "Co-option vasculaire"

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García-Gómez, Pedro, and Manuel Valiente. "Vascular co-option in brain metastasis." Angiogenesis 23, no. 1 (2019): 3–8. http://dx.doi.org/10.1007/s10456-019-09693-x.

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García-Gómez, Pedro, Diana Retana, Pablo Sanz-Martínez, et al. "Abstract 3516: Metastatic colonization requires a proliferative pause linked to vascular co-option." Cancer Research 83, no. 7_Supplement (2023): 3516. http://dx.doi.org/10.1158/1538-7445.am2023-3516.

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Abstract The physical interaction between metastasis-initiating cells and the pre-existing capillary network (a process known as vascular co-option) is critical during the initial stages of multi-organ metastasis in cancer. As such, this process might provide an opportunity to prevent metastasis. As part of the process of vascular co-option, we observed that brain metastatic cells in the perivascular niche temporarily enter into a novel cell state characterized by a decreased proliferation before resuming their aggressive growth to colonize the organ. Transcriptomic analysis of co-opting metas
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Takano, Shingo, Toshihide Tanaka, Eiichi Ishikawa, et al. "ANGI-05 PATHOGENESIS OF RESISTANCE (MIMICRY AND CO-OPTION) TO ANTI-ANGIOGENIC TREATMENT FOR GLIOBLASTOMA." Neuro-Oncology Advances 1, Supplement_2 (2019): ii5. http://dx.doi.org/10.1093/noajnl/vdz039.020.

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Abstract PURPOSE Vessel co-option and vascular mimicry are important resistant factors with ant-angiogenic treatment for glioblastoma, but those precise evaluation is not clear. We had three types of glioblastoma surgically removed specimens treated with / without bevacizumab (Bev). Using these samples, pathogenesis of co-option and mimicry was morphometrically clarified. MATERIALS / METHODS Three types of glioblastoma specimens were analyzed; 1) Bev naive (N group, n 14), 2) Bev effective that was treated preoperative neoadjuvant Bev (E group, n 5), 3) Bev refractory that recurred with contin
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Dudley, Andrew C. "Introduction to special issue: vascular co-option in cancer." Angiogenesis 23, no. 1 (2019): 1–2. http://dx.doi.org/10.1007/s10456-019-09699-5.

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Qian, Chao-Nan. "Hijacking the vasculature in ccRCC—co-option, remodelling and angiogenesis." Nature Reviews Urology 10, no. 5 (2013): 300–304. http://dx.doi.org/10.1038/nrurol.2013.26.

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Annese, Tiziana, Mariella Errede, Antonio d’Amati, et al. "Differential P-Glycoprotein/CD31 Expression as Markers of Vascular Co-Option in Primary Central Nervous System Tumors." Diagnostics 12, no. 12 (2022): 3120. http://dx.doi.org/10.3390/diagnostics12123120.

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Background: Vascular co-option is one of the main features of brain tumor progression. It is identified using histopathological analysis, but no antibody-specific markers were found, and no universally accepted histological features were defined. Methods: We employed double immunohistochemical stainings for CD31, P-gp, S100A10, and mitochondria on formalin-fixed, paraffin-embedded human samples of IDH-WT glioblastoma, IDH-mutant astrocytoma, and meningioma to study vascular co-option across different brain tumors and across normal, peritumoral, and intratumoral areas using the Aperio colocaliz
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Berghoff, Anna Sophie, Orsolya Rajky, Frank Winkler, et al. "Evaluation of invasion patterns and their correlation with integrin alphavbeta expression in brain metastases of solid cancers." Journal of Clinical Oncology 31, no. 15_suppl (2013): 2059. http://dx.doi.org/10.1200/jco.2013.31.15_suppl.2059.

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2059 Background: Understanding the pathobiology of brain metastases (BM) could guide the establishment of new targeted therapies. Methods: We collected 57 autopsy specimens of BM (primary tumor: 27 lung cancer, 6 breast cancer, 8 melanoma, 1 kidney cancer, 2 colorectal cancer, 13 other) and histologically evaluated the patterns of invasion into the surrounding brain parenchyma. Expression of the following integrins was evaluated using immunohistochemistry: with novel antibodies for αv subunit, αvβ3, αvβ5, αvβ6 and αvβ8 integrin. Results: We observed three main invasion patterns: well-demarcate
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Ribatti, Domenico, and Francesco Pezzella. "Overview on the Different Patterns of Tumor Vascularization." Cells 10, no. 3 (2021): 639. http://dx.doi.org/10.3390/cells10030639.

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Angiogenesis is a crucial event in the physiological processes of embryogenesis and wound healing. During malignant transformation, dysregulation of angiogenesis leads to the formation of a vascular network of tumor-associated capillaries promoting survival and proliferation of the tumor cells. Starting with the hypothesis formulated by Judah Folkman that tumor growth is angiogenesis-dependent, this area of research has a solid scientific foundation and inhibition of angiogenesis is a major area of therapeutic development for the treatment of cancer. Over this period numerous authors published
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Seano, Giorgio, and Rakesh K. Jain. "Vessel co-option in glioblastoma: emerging insights and opportunities." Angiogenesis 23, no. 1 (2019): 9–16. http://dx.doi.org/10.1007/s10456-019-09691-z.

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Abstract Vessel co-option is the movement of cancer cells towards and along the pre-existing vasculature and is an alternative to angiogenesis to gain access to nutrients. Vessel co-option has been shown as a strategy employed by some glioblastoma (GBM) cells to invade further into the brain, leading to one of the greatest challenges in treating GBM. In GBM, vessel co-option may be an intrinsic feature or an acquired mechanism of resistance to anti-angiogenic treatment. Here, we describe the histological features and the dynamics visualized through intravital microscopy of vessel co-option in
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Valiente, Manuel, Anna C. Obenauf, Xin Jin, et al. "Serpins Promote Cancer Cell Survival and Vascular Co-Option in Brain Metastasis." Cell 156, no. 5 (2014): 1002–16. http://dx.doi.org/10.1016/j.cell.2014.01.040.

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Dissertations / Theses on the topic "Co-option vasculaire"

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Kerherve, Mathilde. "Étude des mécanismes d’invasion et d’expansion des cellules souches de Glioblastome." Electronic Thesis or Diss., Nantes Université, 2024. http://www.theses.fr/2024NANU1038.

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Le glioblastome (GB) est le cancer le plus courant et le plus agressif du système nerveux central chez l'adulte. Malgré un traitement multimodal incluant chirurgie, radiothérapie, et chimiothérapie, la survie médiane reste limitée a environ 15 mois. Cette issue défavorable s'explique par ('infiltration tumorale dans des régions cérébrales critiques, et, par la résistance aux traitements et les capacités d'expansion des cellules tumorales. Parmi celles-ci, les cellules de type souche de glioblastome (GSCs) jouent un rôle central dans la croissance, l'invasion, et la récidive. Localisées dans de
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Book chapters on the topic "Co-option vasculaire"

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Wang, Sarah, and Andrew C. Dudley. "Vascular Co-option in the Brain Tumor Microenvironment." In Biomarkers of the Tumor Microenvironment. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-98950-7_32.

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Annese, Tiziana, Mariella Errede, Michelina De Giorgis, Loredana Lorusso, Roberto Tamma, and Domenico Ribatti. "Double Immunohistochemical Staining on Formalin-Fixed Paraffin-Embedded Tissue Samples to Study Vascular Co-option." In Methods in Molecular Biology. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2703-7_8.

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García-Gómez, Pedro, and Manuel Valiente. "Vascular co-option." In Tumor Vascularization. Elsevier, 2020. http://dx.doi.org/10.1016/b978-0-12-819494-2.00003-1.

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Herzig, Samuel, Elilary Montilla Medrano, and Karina Gritchenko. "Regional Anesthesia." In Vascular Anesthesia Procedures. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780197506073.003.0015.

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Patients presenting for vascular surgery typically have significant comorbidities. Procedures can vary from minor to quite large with significant blood loss and fluid shifts, and can be elective or emergent. Perioperative morbidity and mortality in the context of co-existing cardiovascular disease, diabetes, dementia and other factors all provide great concern to the anesthesiologist in their approach towards the vascular patient. The anesthetic approach to such patients must therefore be taken with great forethought. Many times, these procedures can be localized to a particular extremity or well-defined set of dermatomes, and regional anesthesia has become one important option for the complicated vascular patient. In this chapter, the risks, benefits, and feasibility of various regional techniques are discussed in the context of patients presenting for carotid endarterectomy, vascular access placement, and major lower extremity vascular surgery.
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Conference papers on the topic "Co-option vasculaire"

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Vermeulen, PB, P.-J. van Dam, S. Daelemans, et al. "Abstract PD9-08: Breast cancer liver metastases vascularize by vessel co-option, not angiogenesis, and have a desert immune phenotype: A histopathological and gene expression study." In Abstracts: 2018 San Antonio Breast Cancer Symposium; December 4-8, 2018; San Antonio, Texas. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-pd9-08.

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