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Cellular senescence, cancer and aging Buck Institute for Age Research Lawrence Berkeley National Laboratory September 10, 2005 SENS2, Cambridge.

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Presentation on theme: "Cellular senescence, cancer and aging Buck Institute for Age Research Lawrence Berkeley National Laboratory September 10, 2005 SENS2, Cambridge."— Presentation transcript:

1 Cellular senescence, cancer and aging Buck Institute for Age Research Lawrence Berkeley National Laboratory September 10, 2005 SENS2, Cambridge

2 Suppressing cancer costs -- aging Tumor Suppressor mechanisms Aging Phenotypes Care- takers (prevent/ repair DNA damage, mutations) Gate- keepers (eliminate/arrest damaged, mutant cells) Apoptosis Senescence Deplete proliferating/ stem cell pools ---> Tissue atrophy/degeneration Deplete proliferating/stem pools Cell dysfunction ---> loss of tissue function/homeostasis Late life phenotypes, including cancer (antagonistic pleiotropy) Longevity assurance

3 Cellular Senescence Suppresses Cancer Cancer cells acquire mutations that abrogate the senescence response Mutations that dampen cellular senescence greatly increase susceptibility to cancer Cellular senescence is controlled by two powerful gatekeeper tumor suppressor pathways (p53 and pRB) Mouse model, human tumor data ----> importance of cell senescence for limiting cancer progression

4 Short/dysfunctional telomeres (REPLICATIVE SENESCENCE) DNA Damage Oncogenes Chromatin Instability Supraphysiological Mitogenic/ Stress Signals Cellular Senescence Induced by Many (Cancer-Causing) Stimuli Irreversible arrest of cell proliferation

5 CELLULAR SENECENCE: Complex Senescent Phenotype Irreversible Growth Arrest Resistance to Apoptosis Altered Function/Gene Expression

6 The senescent phenotype: Altered pattern of gene expression Cell cycle regulation Cell structure Metabolism Biologically active secreted molecules Proteinases Cytokines Growth factors

7 Epithelial Cells Fibroblasts AGE INCIDENCE Mutations Senescent cells CANCER

8 Do senescent cells disrupt normal and/or neoplastic tissue structure/function? (effects of senescent stromal fibroblasts on epithelial cells) Jean-Philippe Coppe, Pierre Desprez, Ana Krtolica, Simona Parrinello, Christopher Patil

9 Senescent fibroblasts disrupt morphology and function of mammary epithelial cells BM + PreS Fb BM + Sen Fb  -casein DAPI Pre-S Fb Sen Fb  -casein E-cadherin Parrinello et al., J Cell Sci, 2005

10 Presenescent fibroblasts Primary duct Secondary duct Senescent fibroblasts Core Core Area Number PRIMARY SECONDARYTERTIARY Senescent fibroblasts disrupt ductal morphogenesis of normal mammary epithelial cells Parrinello et al., J Cell Sci, 2005

11 Senescent fibroblasts stimulate proliferation of premalignant and malignant epithelial cells Krtolica A et al., Proc Natl Acad Sci, 2001

12 Senescent Fibroblasts Stimulate Tumorigenesis of Premalignant Epithelial Cells In Vivo Days 4080120 Tumor size (mm 3 x 10) 100 0 0 200 100 0 200 SCp2 cells alone + Presenescent Fibroblasts + Senescent Fibroblasts Krtolica A et al., Proc Natl Acad Sci, 2001

13 Modeling effects of senescent cells in the mouse: Oxygen matters

14 Senescent phenotype of mouse fibroblasts Mouse cells undergo rapid replicative senescence in culture, despite long telomeres + telomerase Presenescent Senescen t SCp2 HaCATS1 Epithelial Cell Growth HaCATSCp2 S1 Human Fibroblasts Mouse Fibroblasts (MEFs)

15 Severe oxidative damage causes replicative senescence of murine cells in culture Parrinello et al., Nature Cell Biol, 2003

16 How do senescent cells influence the behavior of neighboring cells?

17 The senescence-associated secretory phenotype is conserved and complex Jean-Philippe Coppe, Pierre Desprez, Ana Krtolica, Simona Parrinello, Christopher Patil

18 Conclusions from antibody arrays Senescent stromal cells overexpress/secrete many cytokines, proteases, growth factors (senescence secretory phenotype) There are similarities in the secretory phenotypes of senescent human and mouse stromal cells, BUT oxygen matters There are many similarities among cells induced to senesce by different stimuli

19 Can the senescent phenotype be reversed without reversing the senescent growth arrest?

20 Parrinello et al., J Cell Sci, 2005 Senescent fibroblasts stimulate MEC ductal hyperplasia through MMP-3

21 THANKS! Jean-Philippe Coppe Ana Krtolica Christopher Patil Simona Parrinello (U College London) Christian Beausejour (McGill U) Pierre Desprez -- CPMC Joe Gray, Rich Neve -- LBNL Kalin Kauser -- Berlex


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