Search results for "B16"

showing 9 items of 9 documents

Peroxisome proliferator-activated receptor alpha deficiency impairs regulatory T cell functions: Possible application in the inhibition of melanoma t…

2016

International audience; Regulatory T (Treg) cells are important to induce and maintain immunological self-tolerance. Although the progress accomplished in understanding the functional mechanism of Treg cells, intracellular molecules that control the mechanisms of their suppressive capacity are still on investigation. The present study showed that peroxisome proliferator-activated receptor-alpha deficiency impaired the suppressive activity of Treg cells on CD4(+)CD25(-) and CD8(+) T cell proliferation. In Treg cells, PPARα gene deletion also induced a decrease of migratory abilities, and downregulated the expression of chemokine receptors (CCR-4, CCR-8 and CXCR-4) and p27(KIP1) mRNA. Treg ce…

0301 basic medicineMaleAdoptive cell transferMESH: Tumor BurdenB16 melanoma tumorMelanoma ExperimentalMESH: T-Lymphocyte SubsetsCD4(+)CD25(+) regulatory T cellsBiochemistryMESH: Mice KnockoutImmunotherapy AdoptiveT-Lymphocytes RegulatoryPPARαMESH : T-Lymphocytes RegulatoryCell MovementT-Lymphocyte SubsetsMESH: Reverse Transcriptase Polymerase Chain ReactionMESH : Cell ProliferationMESH : Cell MovementMESH: AnimalsIL-2 receptorMESH: PPAR alphaMESH: Cell MovementCells CulturedMice KnockoutMESH : Melanoma ExperimentalbiologyMESH : Tumor BurdenReverse Transcriptase Polymerase Chain ReactionMESH : Reverse Transcriptase Polymerase Chain ReactionFOXP3hemic and immune systemsGeneral MedicineMESH: Gene Expression Regulation Neoplastic3. Good healthTumor BurdenMESH: Melanoma ExperimentalDNA-Binding ProteinsGene Expression Regulation Neoplasticmedicine.anatomical_structureMESH: Immunotherapy AdoptiveReceptors ChemokineMESH : DNA-Binding ProteinsMESH: Cells Culturedmedicine.medical_specialtyMESH : Receptors ChemokineMESH: Cell Line TumorRegulatory T cellMESH : Gene Expression Regulation NeoplasticT cellMESH : MaleMESH : PPAR alphachemical and pharmacologic phenomenaMESH : Mice Inbred C57BLMESH : Clonal Anergy03 medical and health sciencesMESH: Mice Inbred C57BLInternal medicineMESH: Cell ProliferationCell Line TumorMESH : Cells CulturedmedicineAnimals[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyPPAR alpha[ SDV.BBM ] Life Sciences [q-bio]/Biochemistry Molecular BiologyCell ProliferationClonal AnergyPerforinMESH : Cell Line TumorMESH: T-Lymphocytes RegulatoryMolecular biologyMESH: MaleMESH : T-Lymphocyte SubsetsGranzyme BMice Inbred C57BL030104 developmental biologyEndocrinologyPerforinMESH: Clonal Anergybiology.proteinMESH : Mice KnockoutMESH : AnimalsMESH: Receptors ChemokineCD8MESH: DNA-Binding ProteinsMESH : Immunotherapy Adoptive
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P0311 : Balb/c and C57/Bl6 mice exhibit differences in their susceptibility and anti-tumor response to B16F10 melanoma liver metastasis

2015

Antitumor activityC57 bl6 miceHepatologybiologybusiness.industryCancer researchMedicineB16f10 melanomabusinessbiology.organism_classificationmedicine.diseaseBALB/cMetastasisJournal of Hepatology
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Singular solutions to a quasilinear ODE

2005

In this paper, we prove the existence of infinitely many radial solutions having a singular behaviour at the origin for a superlinear problem of the form $-\Delta_pu=|u|^{\delta-1}u$ in $B(0,1)\setminus\{0\}\subset\mathbb R^N$,\, $u=0$ for $|x|=1$, where $N>p>1$ and $\delta>p-1$. Solutions are characterized by their nodal properties. The case $\delta+1 <\frac{Np}{N-p}$ is treated. The study of the singularity is based on some energy considerations and takes into account the classification of the behaviour of the possible solutions available in the literature. By following a shooting approach, we are able to deduce the main multiplicity result from some estimates on the rotation numbers asso…

Applied Mathematics34B1634B15Singular solutions superlinear problem multiplicity result p-Laplacian equation rotation number radial solutionsAnalysis35J60
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In vivo effects of tumor necrosis factor-α or flavone acetic acid in combination with doxorubicin on multidrug-resistant B16 melanoma

1996

Having observed that tumor necrosis factor (TNF)-alpha and doxorubicin (DXR) produce a synergistic inhibition of melanoma B16 and also of its multidrug resistant (MDR) variant in vitro, we tested whether this interaction would occur in vivo as well. C57BL/6 mice with s.c. tumors were treated with TNF or flavone acetic acid (FAA), a biological response modifier, in simultaneous or sequential combination with DXR. The agents were administered systemically. Overall, the results were negative, apart from a trend towards slight synergy, found in the chemosensitive melanoma, when TNF was given 1 or 2 days before DXR. The effects of FAA and DXR were found to be subadditive or antagonistic. However…

Cancer ResearchSkin NeoplasmsMelanoma ExperimentalMiceIn vivoAntineoplastic Combined Chemotherapy ProtocolsmedicineAnimalsPharmacology (medical)DoxorubicinFlavonoidsPharmacologyAntibiotics AntineoplasticFlavone acetic acidDose-Response Relationship DrugTumor Necrosis Factor-alphaChemistryMelanomamedicine.diseaseDrug Resistance MultipleIn vitroMultiple drug resistanceOncologyBiochemistryDoxorubicinDrug Resistance NeoplasmCancer researchFemaleTumor necrosis factor alphaB16 melanomamedicine.drugAnti-Cancer Drugs
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Immigrant status, gender, and school burnout in Finnish lower secondary school students : A longitudinal study

2017

The aim of this longitudinal study among 9223 students from grade 7 and grade 9 (age 13–14 and 15–16) was to assess whether immigrant status and gender are associated with the level and change (slope) in school burnout among lower secondary school students in the Helsinki metropolitan area. Ninety-seven percent of the variation in school burnout was attributable to individual factors. Both the intercept (2.3, p &lt; 0.001) and slope (0.5, p &lt; 0.001) of school burnout were statistically significant. The slope showed increasing school burnout from grades 7–9. School burnout increased more in girls than in boys. Initially apparent higher school burnout among students who had immigrated to …

Longitudinal studySocial Psychologymedia_common.quotation_subjecthealth care facilities manpower and servicesImmigrationeducationkoulu (ilmiöt)Context (language use)pitkittäistutkimusBurnoutuupumusEducationsukupuolischool (phenomena)immigrant statusDevelopmental Neuroscienceupper comprehensive schoolHN Social history and conditions. Social problems. Social reformPedagogyexhaustionDevelopmental and Educational Psychology0501 psychology and cognitive sciencesStatistical analysis10. No inequalityLife-span and Life-course Studieslower secondary schoolta515media_commonLB1603 Secondary Education. High schools4. Education05 social sciencesMultilevel model050301 educationschool burnoutmaahanmuuttajatyläkouluPsychology0503 educationSocial Sciences (miscellaneous)psychological phenomena and processes050104 developmental & child psychologyClinical psychologyInternational Journal of Behavioral Development
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Effects of gamma interferon on a B16 melanoma cell line and its doxorubicin-resistant variant.

1992

PharmacologyDoxorubicin resistantbusiness.industryDrug ResistanceMelanoma ExperimentalBiologyVirologyMajor Histocompatibility ComplexInterferon-gammaText miningCell cultureAntigens NeoplasmDoxorubicinGamma interferonTumor Cells CulturedbusinessB16 melanomaPharmacological research
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Dacarbazine mediate antimelanoma effects via NK cells.

2013

International audience; Melanoma is a highly chemoresistant and metastatic tumor that, in the absence of BRAF mutations, is generally treated with the alkylating agent dacarbazine (DTIC). We discovered that DTIC upregulates the expression of NKG2D ligands on tumor cells, leading to the activation of natural killer (NK) and CD8(+) T cells. These observations underscore the immunogenic properties of DTIC and provide a rationale to combine DTIC with immunotherapeutic agents.

[SDV.IMM] Life Sciences [q-bio]/ImmunologyDacarbazineImmunologyNkg2d ligandsTumor cellschemical and pharmacologic phenomenadacarbazineNK cellsMetastatic tumorNKG2DmedicinemelanomaImmunology and Allergy[ SDV.IMM ] Life Sciences [q-bio]/ImmunologyB16Author's Viewbusiness.industryMelanomamedicine.diseaseNKG2D3. Good healthOncologyImmunologyCancer research[SDV.IMM]Life Sciences [q-bio]/ImmunologybusinessCD8medicine.drug
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Targeting the tumor mutanome for personalized vaccination therapy

2012

Next generation sequencing enables identification of immunogenic tumor mutations targetable by individualized vaccines. In the B16F10 melanoma system as pre-clinical proof-of-concept model, we found a total of 563 non-synonymous expressed somatic mutations. Of the mutations we tested, one third were immunogenic. Immunization conferred in vivo tumor control, qualifying mutated epitopes as source for effective vaccines.

next generation sequencingSomatic cellbusiness.industryImmunologyBioinformaticscancer immunogenicityDNA sequencingEpitopeVaccinationOncologyImmunizationIn vivoImmunogenic tumornon-synonymous mutationsCancer researchindividualized therapyImmunology and AllergyMedicinetumor mutationsB16f10 melanomacancer vaccinationbusinessAuthor's ViewOncoImmunology
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Desarrollo y efecto antitumoral de vacunas génicas celulares y silenciamiento génico

2015

La presente tesis utiliza las vacunas antitumorales basadas en células modificadas genéticamente como principal estrategia para intentar lograr una respuesta inmune antitumoral eficaz. La vacunación preventiva con células tumorales modificadas genéticamente ha logrado muy buenos resultados en ratones consiguiendo la inhibición del crecimiento tumoral y la supervivencia final de los mismos. Sin embargo, en la clínica la disponibilidad de ciertas células tumorales es muy baja y su transfección es poco reproducible. Por ello, en esta tesis se plantea como uno de los objetivos principales desarrollar y evaluar el efecto antitumoral de vacunas basadas en complejos celulares formados por células …

terapia génicactla4silenciamiento génicofoxp3melanoma B16oligonucleótidos antisentidoPPRHvacuna antitumorales:CIENCIAS MÉDICAS ::Farmacología ::Evaluación de medicamentos [UNESCO]UNESCO::CIENCIAS MÉDICAS ::Farmacología ::Evaluación de medicamentos
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