CANCAN-RUTGERS

NIH RePORTER · NIH · OT2 · $223,182 · view on reporter.nih.gov ↗

Abstract

Cancer cachexia (CC) is a systemic, metabolic wasting syndrome featuring body weight loss due to skeletal muscle and adipose tissue wasting. CC is suffered by ~80% of cancer patients that causes reduced performance status, intolerance to chemotherapy, and increased mortality. This debilitating condition is poorly understood and has no effective treatment. If CC therapy existed, it would improve treatment responses, increase quality of life, and prolong survival. With 50 years of study, the field has focused on defining pathways that promote atrophy in the end-organs most affected my cachexia. While this work has been fruitful, it has not led to identification of the upstream mediators of CC, nor has it generated effective therapies. There is an urgent need for high-quality discovery science and more detailed clinical phenotyping.We have created a virtual institute comprised of diverse, international, multidisciplinary scientists and clinicians with expertise in cancer, metabolism, neuroendocrine function, immunology, human metabolic diseases, preclinical models, and clinical phenotyping. We hypothesize that CC is driven by tumor-intrinsic factors that activate neurohormonal sickness pathways, which then induce anorexia, metabolic dysfunction, and tissue atrophy.

Key facts

NIH application ID
10621047
Project number
1OT2CA278609-01
Recipient
RBHS -CANCER INSTITUTE OF NEW JERSEY
Principal Investigator
Eileen P. White
Activity code
OT2
Funding institute
NIH
Fiscal year
2022
Award amount
$223,182
Award type
1
Project period
2022-06-22 → 2023-05-31