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The aim of this work is to evaluate the sensitizer potential to antitumoral treatments of a new compound: S-nitrosocaptopril. This molecule possesses a NO moeity and an ACE inhibitor ability. Based on previous studies, we have hypothesized that S-nitrosocaptopril can increase the sensibilisation of tumor by increasing the 02 availability and decreasing the cellular respiration rate. We have investigated this effect by RPE spectryoscopy and MRI. We first evaluated the effect of tumor oxygenation by RPE L-band and have confirmed these results by 19F-MRI. The S-nitrosocaptopril has led to an increase of p02 after thirty minutes and the pression pressure was maintained during thirty more minutes. We have then searched the mechanism by investigating the tumor perfusion by patent blue staining. There was no difference between captopril and S nitrosocaptopril , perhaps because the captopril has elevated too much the blood flow to see any variation. After that, we have tested the ability of S-nitrosocaptopril to inhibit the oxygen consumption in vitro by EPR X-band spectrometer. There was a significant difference between the both treatments and the S-nitrosocaptopril consumes less oxygen than the captopril. We wanted to highlight the presence of NO by spin-trapping but this experiment failed. However, we have found that theS-nitrosocaptopril is superior to the captopril in their effect to increase the p02 in the tumor. It comes from decreasing the consumption of oxygen. The radio- and chemo sensitizer effect of S-nitrosocaptopril need still to be evaluated by assaying tumor regrowth delay assay.
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The aim of this work is based on the hypothesis that some molecules may enhance tumor radiosensitivity by increasing tumor oxygenation (p02). Firstly, the effect of the combination of two treatments (xanthiinol nicotinate and hydrocortisone) was studied using TLT tumor bearing mice, using electron paramagnetic resonance oximetry (EPR). No result was observed. Secondly, the effect of prostaglandins (PGh and PGE 1) was also tested , using TLT tumor bearing mice. An increased p02 was observed for PGiz (the most powerful endogenous vasodilatator). Nevertheless, embolisms at the injection site were observed, requiring changing the administration route. For PGE 1, EPR data clearly demonstrated an increase PO². These results were confirmed by others studies using relaxometry. Together our results show the potential usefulness of the administration of PGE 1 before irradiation L'objectif de ce travail est basé sur l'hypothèse que certaines molécules peuvent améliorer la radiosensibilité tumorale via l'augmentation de l'oxygénation tumorale ( PO²i). Premièrement, l’effet d'une combinaison de deux traitements (xanthinol nicotinate et hydrocortisone) a été étudié sur des souris porteuses d'une tumeur TLT, par oxymétrie par résonance paramagnétique électronique (RPE). Les résultats obtenus ne furent pas concluants. Deuxièmement, l'effet de prostaglandines (PGli et PGE 1) a également été testé sur des souris porteuses de tumeurs TLT. Une augmentation de p02 a pu être observée pour la PGh (vasodilatateur endogène le plus puissant). Néanmoins des phénomènes d'embolie au site d'injection obligeraient de changer la voie d'administration. Pour la PGE 1, des études de RPE ont clairement démontré une nette augmentation de la p02.Ces résultats ont été confirmés par des études de relaxométrie au fluor 19. Ces résultats montrent la potentielle utilité de l'administration de la PGE 1 avant l'irradiation.
Xanthinol Niacinate --- Hydrocortisone --- Prostaglandin Antagonists --- Tumor Microenvironment
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This eBook is a collection of articles from a Frontiers Research Topic. Frontiers Research Topics are very popular trademarks of the Frontiers Journals Series: they are collections of at least ten articles, all centered on a particular subject. With their unique mix of varied contributions from Original Research to Review Articles, Frontiers Research Topics unify the most influential researchers, the latest key findings and historical advances in a hot research area! Find out more on how to host your own Frontiers Research Topic or contribute to one as an author by contacting the Frontiers Editorial Office: frontiersin.org/about/contact
tumor microenvironment --- monocyte --- macrophage --- neutrophil --- immunosuppression --- immunotherapy
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Mesothelioma is a rare aggressive cancer that develops from the mesothelium. Recent molecular analyses have defined four different types of mesothelioma based on gene expression and two major molecularly-defined groups based on prognosis. In this volume, potential mechanisms causing this heterogeneity are explored. The different chapters include heterogeneity learned from experimental animal models in NF2/Hippo pathway signaling, stem cell signaling pathways, the tumor microenvironment, and micro RNA secretome. Novel aspects deserving attention such as the implication of long, non-coding RNA in disease heterogeneity are described. The volume also includes the description of tools useful to address some specific questions such as an assessment of the copy number variations of two tumor suppressors frequently mutated in mesothelioma or an investigation of Macrophage Inhibition Factor signaling in mesothelioma.
NF2 signaling pathway --- tumor microenvironment --- mesothelioma --- experimental mesothelioma models
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This eBook is a collection of articles from a Frontiers Research Topic. Frontiers Research Topics are very popular trademarks of the Frontiers Journals Series: they are collections of at least ten articles, all centered on a particular subject. With their unique mix of varied contributions from Original Research to Review Articles, Frontiers Research Topics unify the most influential researchers, the latest key findings and historical advances in a hot research area! Find out more on how to host your own Frontiers Research Topic or contribute to one as an author by contacting the Frontiers Editorial Office: frontiersin.org/about/contact
Medicine --- Immunology --- tumor microenvironment --- monocyte --- macrophage --- neutrophil --- immunosuppression --- immunotherapy
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Gastrointestinal system --- Cancer. --- Gastrointestinal Neoplasms --- Immunotherapy. --- Tumor Microenvironment. --- immunology.
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This book provides a state-of-the-art review of the biology, treatment, and other critical aspects of neuroblastoma, reflecting the dramatic advances that have been achieved in understanding and management. Topics are arranged according to the book’s dominant themes of the “seed” (tumor genomics, epigenetics, metabolism, and stem cells) and the “soil” (tumor microenvironment, adaptive and innate immunity, and exosomes) and how both of these influences can serve as rich targets for intervention, whether by targeted molecular therapy or immunotherapy. Therapeutic strategies that are currently in use or under consideration for the future are discussed in detail, with the focus on precision medicine. Further individual chapters are devoted to the biology and genetics of relapsed/refractory neuroblastoma and emerging methods of evaluating tumor burden. Finally, in keeping with the, albeit modest, increase in cure rates in high-risk disease, immune and cellular therapies are reviewed. This coverage of what is becoming a not-so-enigmatic tumor will appeal to a broad readership including both experimental oncologists and clinicians who care for patients with neuroblastoma.
Oncology. --- Pediatrics. --- Neurology. --- Neuroblastoma. --- Precision Medicine. --- Tumor Microenvironment.
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Flax. --- Tamoxifen. --- Breast Neoplasms. --- Breast. --- Cellular Microenvironment. --- Tumor Microenvironment.
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This eBook is a collection of articles from a Frontiers Research Topic. Frontiers Research Topics are very popular trademarks of the Frontiers Journals Series: they are collections of at least ten articles, all centered on a particular subject. With their unique mix of varied contributions from Original Research to Review Articles, Frontiers Research Topics unify the most influential researchers, the latest key findings and historical advances in a hot research area! Find out more on how to host your own Frontiers Research Topic or contribute to one as an author by contacting the Frontiers Editorial Office: frontiersin.org/about/contact
Medicine --- Immunology --- tumor microenvironment --- monocyte --- macrophage --- neutrophil --- immunosuppression --- immunotherapy
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Multifaceted Role of IL-1 in Cancer and Inflammation summarizes the existing literature and discusses future perspectives about the role of IL-1 in immune suppression, cancer progression, angiogenesis, and resistance to immunotherapies. The book presents mechanisms to overcome IL-1 mediated immune suppression in tumor microenvironment and covers topics on the source of IL-1 in the tumor microenvironment, IL-1 mediated downstream pathway, mechanism of IL-1 mediated immune suppression in cancer, and its effect on immunotherapy of cancer. Those topics help readers understand the effect of IL-1 on cancer immunopathology and immunotherapy, and provide them with broader concepts to develop therapies for IL-1 enrichment tumors.
Cancer --- Immunological aspects. --- Carcinogenesis --- Immunological aspects --- Interleukin-1 --- Neoplasms --- Immunotherapy --- Tumor Microenvironment --- Immunology. --- immunology --- Interleukin-1. --- Immunotherapy. --- Tumor Microenvironment. --- immunology.
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