Narrow your search

Library

ULiège (5)

FARO (4)

KU Leuven (4)

LUCA School of Arts (4)

Odisee (4)

Thomas More Kempen (4)

Thomas More Mechelen (4)

UCLL (4)

ULB (4)

VIVES (4)

More...

Resource type

book (10)

dissertation (1)


Language

English (11)


Year
From To Submit

2022 (1)

2021 (6)

2020 (3)

2019 (1)

Listing 1 - 10 of 11 << page
of 2
>>
Sort by

Dissertation
Thesis, COLLÉGIALITÉ
Authors: --- --- --- ---
Year: 2022 Publisher: Liège Université de Liège (ULiège)

Loading...
Export citation

Choose an application

Bookmark

Abstract

Lymphangiogenesis consists in the formation of new lymphatic vessels from already&#13;established ones. This complex biological process is triggered during inflammation, wound repair or cancer. A decrease or defect in lymphangiogenesis leads to a pathology called lymphedema. This condition is characterised by tissue swelling caused by the accumulation of interstitial fluids. Nowadays there is no curative therapy. Vascular Endothelial Growth Factor Receptors 2 and 3 (VEGFR 2/3) represent interesting therapeutic targets as they are known to be major lymphangiogenesis inducers. Previous work from the host laboratory has identified the endocytic receptor “urokinase plasminogen activator receptor-associated protein” (“uPARAP” encoded by MRC2 gene) as negatively regulating lymphangiogenesis. uPARAP interacts with VEGFR 2/3 and blocks their heterodimerisation and signalisation. More recently, the laboratory has identified the interaction of uPARAP with Vascular Endothelial cadherin (VE-cadherin), a transmembrane protein also known to play key roles in lymphangiogenesis.&#13;The aim of this work is to identify the binding site between uPARAP and VE-cadherin or VEGFR 2/3 in order to provide better knowledge on uPARAP’s functions in lymphatics.&#13;A collaboration with Pr. Miikka Vikkula (UCL) had previously identified 7 uPARAP variants from a primary lymphedema patient cohort. We generated and validated upon this work multiple engineered A431 cell lines to express some known uPARAP partners (VE- cadherin, VEGF-R2 and VEGF-R3). Through proximity ligation assays, we successfully identified two variants (Thr653Met, Arg680Trp) who decreased uPARAP interactions with VE- cadherin. Finally, we tried but failed to produce new lentiviral vectors containing the previously identified variants. Those vectors were though to permit the investigation of variant impacts in primary human lymphatic endothelial cells Le processus de génération de nouveaux vaisseaux sanguins à partir de vaisseaux&#13;préexistants est appelé ‘’lymphangiogenèse’’. Ce processus biologique complexe est déclenché pendant l’inflammation, lors des processus de réparation des tissus ou boen encore lors de cancers. Une diminution ou un défaut de lymphangiogenèse mène au développement d’une pathologie appelée ‘’lymphoedème’’. Cette pathologie est chartérisée par le gonflement des tissus causé par une accumulation de fluides au sein des tissus. Aucune thérapie n’existe actuellement pour soigner définitivement cette pathologie. Les récepteurs aux facteurs de croissance vasculaire endothélial (vascular endothelial growth factor receptors -VEGFRs-) de type 2 et 3 (VEGF-R2 et VEGF-R3) forment des cibles thérapeutiques intéressantes de par leurs rôles majeurs dans l’induction et la régulation de la lymphangiogenèse. De précédent travaux au sein du laboratoire d’accueil ont identifié le récepteur endocytique ‘’urokinase plasminogen activator receptor-associated protein’’ (uPARAP, produit de l’expression du gene MRC2) comme régulant négativement la lymphangiogenèse. uPARAP inhibe la formation d’hétérodimeres VEGF-R2/VEGF-R3 et bloque ainsi leur signalisation. Plus récemment, le laboratoire d’accueil a identifié l’interaction d’uPARAP avec la vascular endothelial cadherin (VE-cadherin), une protein transmembranaire également connue dans la lymphangiogenèse.&#13;Le but de ce travail est d’identifier le ou les site(s) de liaison d’uPARAP avec ses différents partenaires (VE-cadherin ou VEGF-R2/R3) afin d’obtenir une plus profonde connaissance des fonctions d’uPARAP dans le système lymphatique.&#13;En collaboration avec le Professeur Miikka Vikkula (UCL), 7 variants ont précédemment été identifiés. Au cours de ce travail, nous avons induit et validé l’expression de la VE-cadherin at des VEGF-R2 et R3 dans une lignée de cellules cancéreuses (A431). Nous avons ensuite identifié avec succès deux variants (Thr653Met, Arg680Trp) diminuant l’interaction d’uPARAP avec la VE-cadherin. Enfin, nous avons essayé mais échoué à produire de nouveau vecteurs lentiviraux contenant les différents variants. Ces vecteurs étaient destinés à l’évaluation de l’impact des variants au sein de cellules endothéliales lymphatiques humaines.


Book
New Aspects of Cancer Stem Cell Biology : Implications for Innovative Therapies
Authors: ---
Year: 2020 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

The cancer stem cell (CSC) paradigm represents one of the most prominent breakthroughs of the last decades in tumor biology. CSCs are that subpopulation within a tumor that can survive conventional therapies and as a consequence are able to fuel tumor recurrence. Nevertheless, the biological characteristics of CSCs and even their existence, remain the main topic among tumor biologists debates. The difficulty in achieving a better definition of CSC biology may actually be explained by the plasticity of such a cell subpopulation. Indeed, the emerging view is that CSCs represent a dynamic “state” of tumor cells that can acquire stemness-related properties under specific circumstances, rather than referring to a well-defined group of cells. Regardless of their origin, it is clear that designing novel antitumor treatments based on the eradication of CSCs will only be possible upon unraveling the biological mechanisms that underlie their pathogenic role in tumor progression and therapy resistance. The Special Issue on “New aspects of cancer stem cell biology: implications for innovative therapies” aims at highlighting recent insights into CSC features that can make them an attractive target for novel therapeutic strategies.


Book
New Aspects of Cancer Stem Cell Biology : Implications for Innovative Therapies
Authors: ---
Year: 2020 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

The cancer stem cell (CSC) paradigm represents one of the most prominent breakthroughs of the last decades in tumor biology. CSCs are that subpopulation within a tumor that can survive conventional therapies and as a consequence are able to fuel tumor recurrence. Nevertheless, the biological characteristics of CSCs and even their existence, remain the main topic among tumor biologists debates. The difficulty in achieving a better definition of CSC biology may actually be explained by the plasticity of such a cell subpopulation. Indeed, the emerging view is that CSCs represent a dynamic “state” of tumor cells that can acquire stemness-related properties under specific circumstances, rather than referring to a well-defined group of cells. Regardless of their origin, it is clear that designing novel antitumor treatments based on the eradication of CSCs will only be possible upon unraveling the biological mechanisms that underlie their pathogenic role in tumor progression and therapy resistance. The Special Issue on “New aspects of cancer stem cell biology: implications for innovative therapies” aims at highlighting recent insights into CSC features that can make them an attractive target for novel therapeutic strategies.


Book
New Aspects of Cancer Stem Cell Biology : Implications for Innovative Therapies
Authors: ---
Year: 2020 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

The cancer stem cell (CSC) paradigm represents one of the most prominent breakthroughs of the last decades in tumor biology. CSCs are that subpopulation within a tumor that can survive conventional therapies and as a consequence are able to fuel tumor recurrence. Nevertheless, the biological characteristics of CSCs and even their existence, remain the main topic among tumor biologists debates. The difficulty in achieving a better definition of CSC biology may actually be explained by the plasticity of such a cell subpopulation. Indeed, the emerging view is that CSCs represent a dynamic “state” of tumor cells that can acquire stemness-related properties under specific circumstances, rather than referring to a well-defined group of cells. Regardless of their origin, it is clear that designing novel antitumor treatments based on the eradication of CSCs will only be possible upon unraveling the biological mechanisms that underlie their pathogenic role in tumor progression and therapy resistance. The Special Issue on “New aspects of cancer stem cell biology: implications for innovative therapies” aims at highlighting recent insights into CSC features that can make them an attractive target for novel therapeutic strategies.


Book
New Prognostic and Predictive Markers in Cancer Progression
Authors: ---
Year: 2021 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

Biomarkers are of critical medical importance for oncologists, allowing them to predict and detect disease and to determine the best course of action for cancer patient care. Prognostic markers are used to evaluate a patient’s outcome and cancer recurrence probability after initial interventions such as surgery or drug treatments and, hence, to select follow-up and further treatment strategies. On the other hand, predictive markers are increasingly being used to evaluate the probability of benefit from clinical intervention(s), driving personalized medicine. Evolving technologies and the increasing availability of “multiomics” data are leading to the selection of numerous potential biomarkers, based on DNA, RNA, miRNA, protein, and metabolic alterations within cancer cells or tumor microenvironment, that may be combined with clinical and pathological data to greatly improve the prediction of both cancer progression and therapeutic treatment responses. However, in recent years, few biomarkers have progressed from discovery to become validated tools to be used in clinical practice. This Special Issue comprises eight review articles and five original studies on novel potential prognostic and predictive markers for different cancer types.


Book
New Prognostic and Predictive Markers in Cancer Progression
Authors: ---
Year: 2021 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

Biomarkers are of critical medical importance for oncologists, allowing them to predict and detect disease and to determine the best course of action for cancer patient care. Prognostic markers are used to evaluate a patient’s outcome and cancer recurrence probability after initial interventions such as surgery or drug treatments and, hence, to select follow-up and further treatment strategies. On the other hand, predictive markers are increasingly being used to evaluate the probability of benefit from clinical intervention(s), driving personalized medicine. Evolving technologies and the increasing availability of “multiomics” data are leading to the selection of numerous potential biomarkers, based on DNA, RNA, miRNA, protein, and metabolic alterations within cancer cells or tumor microenvironment, that may be combined with clinical and pathological data to greatly improve the prediction of both cancer progression and therapeutic treatment responses. However, in recent years, few biomarkers have progressed from discovery to become validated tools to be used in clinical practice. This Special Issue comprises eight review articles and five original studies on novel potential prognostic and predictive markers for different cancer types.


Book
New Prognostic and Predictive Markers in Cancer Progression
Authors: ---
Year: 2021 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

Biomarkers are of critical medical importance for oncologists, allowing them to predict and detect disease and to determine the best course of action for cancer patient care. Prognostic markers are used to evaluate a patient’s outcome and cancer recurrence probability after initial interventions such as surgery or drug treatments and, hence, to select follow-up and further treatment strategies. On the other hand, predictive markers are increasingly being used to evaluate the probability of benefit from clinical intervention(s), driving personalized medicine. Evolving technologies and the increasing availability of “multiomics” data are leading to the selection of numerous potential biomarkers, based on DNA, RNA, miRNA, protein, and metabolic alterations within cancer cells or tumor microenvironment, that may be combined with clinical and pathological data to greatly improve the prediction of both cancer progression and therapeutic treatment responses. However, in recent years, few biomarkers have progressed from discovery to become validated tools to be used in clinical practice. This Special Issue comprises eight review articles and five original studies on novel potential prognostic and predictive markers for different cancer types.


Book
Drug delivery technology development in Canada
Authors: ---
ISBN: 3039280058 303928004X Year: 2019 Publisher: MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

Canada continues to have a rich history of ground-breaking research in drug delivery within academic institutions, pharmaceutical industry and the biotechnology community.

Keywords

encapsulation --- biodistribution --- pharmaceutics --- targeted therapies --- gambogic acid --- GE11 peptide --- formulation and dosage form development --- transient modulation --- ROESY NMR spectroscopy --- bioaccessibility --- polymeric micelle --- pharmacological Inhibitors of HIF-1 and STAT3 --- nanoparticles --- Vitamin D --- drug discovery --- EGFR-targeted therapy --- translational research --- clinical trials --- doxorubicin --- dissolution --- drug development --- permeation enhancers --- Canada --- plant --- primary central nervous system lymphomas --- photostabilizers --- head and neck squamous cell carcinoma --- mouse models --- drug delivery systems --- melphalan --- hypoxia-induced chemoresistance --- skin --- virus --- circadian clock --- child friendly formulation --- adenanthin --- co-delivery --- canola oil deodorizer distillate --- Metaplex --- innovation --- controlled drug delivery --- nifedipine --- radiolabeling --- amphotericin B --- biological barriers --- blood-brain barrier (BBB) --- biologicals --- lipid nanoparticles --- oral formulation --- phytosterols --- medical devices --- chronotherapy --- oral --- cationic gemini surfactant --- route of administration --- drug delivery --- intra-arterial chemotherapy --- developing world --- sustained delivery --- water miscible solvents --- combination therapy --- antibodies --- throughput --- magnetic fields --- liposomes --- medulloblastoma --- drug-resistant melanoma --- rosmarinic acid --- topical formulation --- TNO gastrointestinal model --- gastrointestinal simulator --- malignant gliomas --- transdermal drug delivery --- oral delivery --- precision medicine --- 3D spheroid --- flavonoids --- staurosporine --- DOX-Vit D --- loading gradients --- bacteriophage --- phospholipid complex --- triggered drug release --- HIF-1 --- phage display --- pharmacokinetics --- emulsion --- quercetin --- cisplatin --- parasitic infections --- remote loading --- HAV6 cadherin peptide --- blood-brain barrier --- inclusion complex --- tocopherols --- STAT3 --- ultrasound --- liposome --- fungal infections --- magnetic resonance imaging (MRI) --- MG63 --- model orange juice --- radiation --- cancer --- mefloquine --- small molecules --- Drug Delivery Systems --- Delivery systems, Drug --- Drug administration technology --- Drug delivery technology --- Drugs --- Pharmaceutical technology --- Delivery systems


Book
Bacillus thuringiensis Toxins: Functional Characterization and Mechanism of Action
Authors: --- ---
Year: 2021 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

Bacillus thuringiensis (Bt)-based products are the most successful microbial insecticides to date. This entomopathogenic bacterium produces different kinds of proteins whose specific toxicity has been shown against a wide range of insect orders, nematodes, mites, protozoa, and human cancer cells. Some of these proteins are accumulated in parasporal crystals during the sporulation phase (Cry and Cyt proteins), whereas other proteins are secreted in the vegetative phase of growth (Vip and Sip toxins). Currently, insecticidal proteins belonging to different groups (Cry and Vip3 proteins) are widely used to control insect pests and vectors both in formulated sprays and in transgenic crops (the so-called Bt crops). Despite the extensive use of these proteins in insect pest control, especially Cry and Vip3, their mode of action is not completely understood. The aim of this Special Issue was to gather information that could summarize (in the form of review papers) or expand (research papers) the knowledge of the structure and function of Bt proteins, as well as shed light on their mode of action, especially regarding the insect receptors. This subject has generated great interest, and this interest has been materialized into the 18 papers of important scientific value in the field (5 reviews and 13 research papers) that have been compiled in this issue.

Keywords

Research & information: general --- Bacillus thuringiensis --- Plutella xylostella --- Cry1Ac resistance --- trypsin-like midgut protease --- protoxin activation --- Spodoptera spp., Helicoverpa armigera --- Mamestra brassicae --- Anticarsia gemmatalis --- Ostrinia furnacalis --- Cry2Ab toxin --- Bombyx mori --- ATP-binding cassette subfamily a member 2 (ABCA2) --- genome editing --- transcription activator-like effector-nucleases (TALENs) --- HEK293T cell --- functional receptor --- Vip3Aa --- lysosome --- mitochondria --- apoptosis --- Sf9 cells --- Cry1Ab --- oligomer formation --- Sf21 cell line --- Ostrinia nubilalis --- Lobesia botrana --- Leptinotarsa decemlineata --- bioassay --- Cyt2Aa2 toxin --- protein-lipid binding --- erythrocyte membrane --- AFM --- QCM-D --- Asian corn borer --- ABCC2 --- CRISPR/Cas9 --- Cry1Fa --- resistance --- chitin-binding protein --- adhesion --- peritrophic matrix --- Vip3A --- Spodoptera litura --- site-directed mutagenesis --- Cry --- Cyt --- parasporins --- S-layer proteins --- Vip --- Sip --- membrane receptors --- insecticidal activity --- anticancer activity --- Aedes aegypti --- minor proteins --- synergy --- mosquito control --- Bti --- Spodoptera frugiperda --- cadherin --- mode of action of Cry toxin --- insecticidal proteins --- insect resistance --- tobacco budworm --- Bacillus thuringiensis proteins --- coleopteran pests --- structure --- mode of action --- 3D-structure --- biological control --- antimicrobial peptide --- gut microbiota --- vegetative insecticidal proteins --- pyramids --- 3D-Cry toxins --- in vitro evolution --- rational design --- toxin enhancement --- n/a


Book
Bacillus thuringiensis Toxins: Functional Characterization and Mechanism of Action
Authors: --- ---
Year: 2021 Publisher: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute

Loading...
Export citation

Choose an application

Bookmark

Abstract

Bacillus thuringiensis (Bt)-based products are the most successful microbial insecticides to date. This entomopathogenic bacterium produces different kinds of proteins whose specific toxicity has been shown against a wide range of insect orders, nematodes, mites, protozoa, and human cancer cells. Some of these proteins are accumulated in parasporal crystals during the sporulation phase (Cry and Cyt proteins), whereas other proteins are secreted in the vegetative phase of growth (Vip and Sip toxins). Currently, insecticidal proteins belonging to different groups (Cry and Vip3 proteins) are widely used to control insect pests and vectors both in formulated sprays and in transgenic crops (the so-called Bt crops). Despite the extensive use of these proteins in insect pest control, especially Cry and Vip3, their mode of action is not completely understood. The aim of this Special Issue was to gather information that could summarize (in the form of review papers) or expand (research papers) the knowledge of the structure and function of Bt proteins, as well as shed light on their mode of action, especially regarding the insect receptors. This subject has generated great interest, and this interest has been materialized into the 18 papers of important scientific value in the field (5 reviews and 13 research papers) that have been compiled in this issue.

Keywords

Research & information: general --- Bacillus thuringiensis --- Plutella xylostella --- Cry1Ac resistance --- trypsin-like midgut protease --- protoxin activation --- Spodoptera spp., Helicoverpa armigera --- Mamestra brassicae --- Anticarsia gemmatalis --- Ostrinia furnacalis --- Cry2Ab toxin --- Bombyx mori --- ATP-binding cassette subfamily a member 2 (ABCA2) --- genome editing --- transcription activator-like effector-nucleases (TALENs) --- HEK293T cell --- functional receptor --- Vip3Aa --- lysosome --- mitochondria --- apoptosis --- Sf9 cells --- Cry1Ab --- oligomer formation --- Sf21 cell line --- Ostrinia nubilalis --- Lobesia botrana --- Leptinotarsa decemlineata --- bioassay --- Cyt2Aa2 toxin --- protein-lipid binding --- erythrocyte membrane --- AFM --- QCM-D --- Asian corn borer --- ABCC2 --- CRISPR/Cas9 --- Cry1Fa --- resistance --- chitin-binding protein --- adhesion --- peritrophic matrix --- Vip3A --- Spodoptera litura --- site-directed mutagenesis --- Cry --- Cyt --- parasporins --- S-layer proteins --- Vip --- Sip --- membrane receptors --- insecticidal activity --- anticancer activity --- Aedes aegypti --- minor proteins --- synergy --- mosquito control --- Bti --- Spodoptera frugiperda --- cadherin --- mode of action of Cry toxin --- insecticidal proteins --- insect resistance --- tobacco budworm --- Bacillus thuringiensis proteins --- coleopteran pests --- structure --- mode of action --- 3D-structure --- biological control --- antimicrobial peptide --- gut microbiota --- vegetative insecticidal proteins --- pyramids --- 3D-Cry toxins --- in vitro evolution --- rational design --- toxin enhancement --- n/a

Listing 1 - 10 of 11 << page
of 2
>>
Sort by