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PQ6: Therapeutic approaches for autonomic and neuroendocrine dysfunction in cancer cachexia

PQ6: Therapeutic approaches for autonomic and neuroendocrine dysfunction in cancer cachexia
PQ6:癌症恶病质自主神经和神经内分泌功能障碍的治疗方法
批准号:
10303658
负责人:
Daniel L. Marks
金额:
$43.28万
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
未结题
起止时间:
2021-09-10 至 2026-08-31
关键词:
AcuteAddressAdipose tissueAdrenergic AgentsAdrenergic ReceptorAnimalsAnorexiaAtrophicAttenuatedBehaviorBehavioralBody Weight decreasedCachexiaCancer PatientCardiacCardiovascular systemCatabolismChronicChronic DiseaseChronic stressClinical Trials DesignCollaborationsCorticosteroneCorticotropin-Releasing HormoneDataDiseaseEnergy MetabolismEvolutionExhibitsFatigueFunctional disorderGeneticGlucocorticoidsGoalsHumanHypothalamic structureImpairmentInflammatoryInterventionLaboratoriesLeadLethargiesLifeMalignant NeoplasmsMetabolicMetabolic dysfunctionMetabolic syndromeMetabolismModelingMorbidity - disease rateMotivationMusMuscleMuscular AtrophyNerveNeuroendocrinologyNeuronsNeurosecretory SystemsNeurotransmittersNorepinephrineObservational StudyOrganOrganismOutputPancreatic Ductal AdenocarcinomaPathologicPathway interactionsPatientsPeripheralPharmaceutical PreparationsPharmacologic SubstancePharmacologyPhase II Clinical TrialsPhenotypePhysical FunctionPhysiologicalPlasmaPre-Clinical ModelPreventionQuality of lifeReagentResearchRoleSavingsSick RoleSignal TransductionSkeletal MuscleStressSympathetic Nervous SystemSystemic diseaseTestingTherapeuticTherapeutic InterventionTissuesacute stressbehavioral phenotypingbehavioral responsebiological adaptation to stresscancer cachexiacancer typeclinical translationdefined contributiondensitydesignexercise intoleranceexperiencefunctional declinehypothalamic-pituitary-adrenal axismetabolic phenotypemortality riskmouse modelneuroinflammationnew therapeutic targetnovelnovel therapeuticspancreatic cancer patientspancreatic ductal adenocarcinoma modelprospectiveresponsesynergismsystemic inflammatory responsetherapeutically effectivetumortumor growthwasting

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Project Summary: Illness behaviors, metabolic disturbances, and cardiovascular compromise are common in patients with chronic systemic diseases, and contribute substantially to quality of life and ultimate survival. Other illness- induced morbidities including anorexia and lethargy also compromise the ability of patients to recover from life- saving or extending interventions, and diminish the motivational drive to aggressively battle the underlying condition. Although cachexia in cancer patients was described more than two thousand years ago, the central mechanisms underlying this disorder are poorly understood. Furthermore, there is currently no effective pharmaceutical treatment. Cardiovascular impairment is common in all chronic diseases, and can be a presenting complaint in cancer patients, even prior to initiation of therapy. Our laboratory is dedicated to unraveling the basic mechanisms whereby cancer triggers neuroinflammation and subsequent chronic activation of systemic stress responses in patients with cancer. In this proposal, we will focus on understanding the scope and mechanism by which systemic illness induces chronic activation and alteration in the sympathetic nervous system. The significance of this proposal resides in its unique combination of our historical focus on neuroendocrinology and neuroinflammation, with new collaborations and efforts directed at understanding the extent and mechanisms of cardiovascular impairment and sympathetic nervous system plasticity in patients with cancer. The long-term goal of our research is to gain mechanistic understanding of the acute illness response and how it is transitioned into chronic neuroinflammation in all cancer types, in order to develop more effective therapeutic interventions.
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PQ6: Lipocalin-2 as a therapeutic target for prevention of cancer cachexia
PQ6: Lipocalin-2 as a therapeutic target for prevention of cancer cachexia
PQ6: Therapeutic approaches for autonomic and neuroendocrine dysfunction in cancer cachexia
Exosomes as Endocrine Signaling Molecules in Cancer Cachexia
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