diet, metabolic disease and cancers in mouse models joe nadeau chair, department of genetics case...

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Diet, metabolic disease and cancers in mouse models Joe Nadeau Chair, Department of Genetics Case Western Reserve University [email protected]

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Page 1: Diet, metabolic disease and cancers in mouse models Joe Nadeau Chair, Department of Genetics Case Western Reserve University joseph.nadeau@case.edu

Diet, metabolic disease and cancers

in mouse models

Joe NadeauChair, Department of Genetics

Case Western Reserve [email protected]

Page 2: Diet, metabolic disease and cancers in mouse models Joe Nadeau Chair, Department of Genetics Case Western Reserve University joseph.nadeau@case.edu

=+ and

Cancer risk and metabolic disease

Page 3: Diet, metabolic disease and cancers in mouse models Joe Nadeau Chair, Department of Genetics Case Western Reserve University joseph.nadeau@case.edu

Diet-induced obesity:Gene - diet interactions

B6 on HFHS A/J on HFHS B6 on LFLS A/J on LFLS

0 25 50 75 100 125 1500

10

20

30

40

50

60

Age (days)

Bo

dy

We

igh

t (g

ram

s)

N ~ 25, Error Bars = 1 SD

Normaldiet

HF: 58% kcal coconut oil

LF: 11% kcal coconut oil

Calorically balanced

B6 - obese only with a HFHS diet

A/J - lean regardless of diet

Page 4: Diet, metabolic disease and cancers in mouse models Joe Nadeau Chair, Department of Genetics Case Western Reserve University joseph.nadeau@case.edu

0

10

20

30

40

50

60

70

0 100 200 300 400 500

Age (days)

Mea

n W

eig

ht

(gra

ms)

B6 (35-H) (135-H)A/J (35-H) (135-H)B6 (35-L) (135-L)A/J (35-L) (135-L)

Long-term effects of high fat diet

HCC 20 of 34

No NASHNo HCC

Page 5: Diet, metabolic disease and cancers in mouse models Joe Nadeau Chair, Department of Genetics Case Western Reserve University joseph.nadeau@case.edu

B6-HF (5X)

Non-alcoholic steatohepatitis (NASH) in B6

but not A/J mice-steatosis

(40% of liver mass is lipid)

after 100 days on high fat,

but not low fat diet

- hepatitis (inflammation)

- fibrosis- limited cirrhosis

after 400 days

A/J-HF (5X)(A/J LF)(B6 LF)

Page 6: Diet, metabolic disease and cancers in mouse models Joe Nadeau Chair, Department of Genetics Case Western Reserve University joseph.nadeau@case.edu

Diet-induced malignant transformation and hepatocellular carcinoma (HCC)

Dysplastic nodule

HCC

Dysplastic nodulesCycles of cell damage, death and regeneration eventually lead to transformation,NASH - the ‘fertile soil’ in which transformation occurs

Page 7: Diet, metabolic disease and cancers in mouse models Joe Nadeau Chair, Department of Genetics Case Western Reserve University joseph.nadeau@case.edu

Hepatocellular carcinoma (HCC)

• 3rd most common cause of cancer death worldwide• Rapidly growing cause of cancer death in U.S.• Risk factors:

1. Hepatitis B or C2. Chronic alcohol use

• Remaining 30% of “unexplained” cases are frequently associated with obesity, diabetes, non-alcoholic steatohepatitis

~70% of cases(Ken Tanabe, MGH

personal communication)

Page 8: Diet, metabolic disease and cancers in mouse models Joe Nadeau Chair, Department of Genetics Case Western Reserve University joseph.nadeau@case.edu

HCCs in humans and mice

1. Biochemistry2. Histology3. mRNA profiles

1. Molecular pathways (Myc and NFkB)2. miRNA profiles (X-linked cluster)3. Predicted mRNA targets of miRNAs

Liver necrosis, cell deathLiver steatosisLiver proliferationHepatocellular carcinoma

Cardiac degeneration, cell death

Similar features in humans and mice

Page 9: Diet, metabolic disease and cancers in mouse models Joe Nadeau Chair, Department of Genetics Case Western Reserve University joseph.nadeau@case.edu

HCC

No NASHNo HCCNo death

Sudden death

35 days

135 days

Diet-switch prevents HCC

Page 10: Diet, metabolic disease and cancers in mouse models Joe Nadeau Chair, Department of Genetics Case Western Reserve University joseph.nadeau@case.edu

Metabolic Syndrome, NASH, HCC

On High Fat, High Sucrose Diet:

B6 A/J

Obesity

Hypertension

Insulin Resistance

Cardiovascular Disease Risk

X

X

X

X

Genetics of disease

Genetics of health

J. Nadeau and E. Topol, Nat. Genet. 2006; Shao et al. PNAS; JHN et al, in prep

X

Hepatocellularcarcinoma X

Non-alcoholicsteatohepatitis

Page 11: Diet, metabolic disease and cancers in mouse models Joe Nadeau Chair, Department of Genetics Case Western Reserve University joseph.nadeau@case.edu

HCC summary

Diet-induced, rather than genetically-engineered or carcinogen-induced

Similar pathology and molecular features

Two pathways in one strain on the same diet

Diet switch reverses outcome

A similar diet modification may have important implications for prevention

of HCCs in humans

Page 12: Diet, metabolic disease and cancers in mouse models Joe Nadeau Chair, Department of Genetics Case Western Reserve University joseph.nadeau@case.edu

HCC questions

Genetic control of susceptibilitychromosome substitution strains

(Singer et al. Science 2004, Shao et al. PNAS 2008 )

Mechanisms of transformationengineered mutant genes and alternative fats

Diet switch effectsphysiological mechanisms

Interventionsdrugs and diets

Biomarkers

Page 13: Diet, metabolic disease and cancers in mouse models Joe Nadeau Chair, Department of Genetics Case Western Reserve University joseph.nadeau@case.edu

David BuchnerAnnie Hill

Eric Lander, Nate Berger, John Lambris, Mark Daly, Colleen Croniger, Aris Economides,

Ken Tanabe, and Shankar Subramaniam

Jon Giesinger

Soha YazbekHaifeng Shao

Stephanie Doerner