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The Brown FoundationInstitute for Molecular Medicine
Center for Metabolic and Degenerative Diseases
Good Fat vs Bad Fat and Cancer Prevention
Mikhail Kolonin, Ph.D.
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Obesity: white adipose tissue overgrowth
OBES
TY
I
I
“Type 3 diabetes”Alzheimer’s disease
Alzheimer’s disease
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Healthy years beyond age 65:
BMI (body mass index) > 30 kg/m2 18.4% adolescents
35.7% adults
Obesity growing prevalence impact on health
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White and brown adipose (fat) tissue
Brown Fat Tissue
Burns lipids
White Fat Tissue
Stores lipids
Cold
Exercise
Subcutaneous fat
Visceral fat
Sedentary life style
High-calorie diet
Age
Both excess and deficit of fat tissue leads to disease
Obesity
Lipodystrophy
Diabetes
BMI and mortality
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Highlights•WAT browning contributes to high energy expenditure in cancer-associated cachexia•Systemic inflammation and IL-6 induce and sustain WAT browning in cachexia•Inhibition of WAT browning ameliorates the severity of cachexia•Cancer cachexia patients stain positive for UCP1 protein in WAT
Cancer-associated cachexia (CAC) is a wasting syndrome characterized by systemic inflammation, body weight loss, atrophy of white adipose tissue (WAT) and skeletal muscle. Limited therapeutic options are available and the underlying mechanisms are poorly defined. Here we show that a phenotypic switch from WAT to brown fat, a phenomenon termed WAT browning, takes place in the initial stages of CAC, before skeletal muscle atrophy. WAT browning is associated with increased expression of uncoupling protein 1 (UCP1), which uncouples mitochondrial respiration toward thermogenesis instead of ATP synthesis, leading to increased lipid mobilization and energy expenditure in cachectic mice. Chronic inflammation and the cytokine interleukin-6 increase UCP1 expression in WAT, and treatments that reduce inflammation or β-adrenergic blockade reduce WAT browning and ameliorate the severity of cachexia. Importantly, UCP1 staining is observed in WAT from CAC patients. Thus, inhibition of WAT browning represents a promising approach to ameliorate cachexia in cancer patients.
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Nature 513, 100–104 (04 September 2014)