stromal influences on tumor formation and growth joshua b rubin, m.d., ph.d. department of...

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Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington University School of Medicine

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Page 1: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Stromal Influences on Tumor Formation and Growth

Joshua B Rubin, M.D., Ph.D.Department of Pediatrics

Division of Pediatric Hematology/OncologyWashington University School of Medicine

Page 2: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Outline

• Historical perspectives on the mechanisms of oncogenesis

• Hypothetical roles for stroma in oncogenesis

• Experimental evidence for stromal action in oncogenesis and tumor growth

• Stroma in brain tumorigenesis

Page 3: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Somatic Mutation Theory of Carcinogenesis

Cancer is derived from a single somatic cell that has acquired multiple mutations.

This results in:

Activation of proliferation pathwaysInactivation of cell cycle inhibitorsInactivation of apoptotic mechanismsTelomere maintenanceActivation of migration/invasion pathwaysActivation of angiogenic mechanisms

Page 4: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Support for the Somatic Mutation Theory1890: Hansemann notes mitotic abnormalities in cancer cells and postulates that some chromosomes might stimulate proliferation and others might block mitosis.

1914: Boveri observes that specific chromosomal abnormalities are associated with developmental anomalies in sea urchins and proposes that cancer might arise from somatic mutations.

1951: Armitage & Doll postulate the multistage theory of cancer including somatic mutations, genomic rearrangements and changes in tissue interactions.

1960: Nowell & Hungerford discover Philadelphia chromosome (9:22(BCR:ABL)). Soon afterward 8:14 and 8:22 were described (MYC:Ig).

1971: Knudson explains the epidemiology of retinoblastoma in the “two-hit hypothesis” and this work yields the term anti-oncogene or tumor suppressor.

1976: Varmus discovers a cellular homologue (Src) to the transforming protein of Rous Sarcoma Virus, thus identifying the first oncogene.

Page 5: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Observations that challenge the primacy of SMT

Stewart (1981) Injection of teratocarcinoma (TC) cells into mouse blastocyst generated normal tissues including germ cells.

DiBeradino (1982) Nuclear transplant from Lucke’s frog renal carcinoma cells into activated Ova produced normal tadpoles.

Martins-Green (1994) Integration of RSV into chicken genome only produced tumors in the setting of inflammation.

Page 6: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

and

Sternlicht (1999) Expression of stromalysin-1 in mammary gland produced epithelial tumors.

Olumi (1999) Xenograft of normal prostatic ECs and myofibroblasts (CAFs) led to intraepithelial neoplasia while co-injection of immortalized, non-transformed ECs and CAFs led to malignancy.

Maffini (2003) Mammary carcinomas in mouse arose after implantation of normal epithelial cells into mutagenized mammary fat pads but not when mutagenized epithelial cells were implanted into control fat pads.

Page 7: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

How do you explain these findings?

Page 8: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Paget (1889) Tumor cells are like the seeds of plants, carried by the wind in all directions, but only

able to live on congenial soil.

Cancer is a disease of tissue disorganization.

Page 9: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Theoretical support for the tissue organization hypothesis

Inherited cancer predisposition syndromes often result in cancers in a tissue and age restricted fashion.

During normal development organizing centers regulate growth and differentiation.

Page 10: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

What constitutes tumor stroma

• Vascular endothelial cells• Fibroblasts• Adipocytes• Inflammatory cells (mast cells,

phagocytes, microglia)• Matrix

Page 11: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

What kind of roles can we hypothesize for tumor stroma

Participant in oncogenesisRegulator of tumor growthDeterminant of metastasis

Page 12: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Functional interactions between tumor cells and stroma

Mueller & Fusenig (2004) Nature Cancer Reviews

Page 13: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Three dimensional tissue organization:extracellular matrix

Normal breast epithelial cellsIn matrigel cultures

T4-2 breast carcinoma cellsIn matrigel

T4-2 breast carcinoma cellswith reconstituted alpha-dystroglycan

in matrigel

Henry MD, Cohen MB, Campbell KP (2001) Human Pathol 32:791Muschler J et al. (2002) Cancer Res. 62:7102

Page 14: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

The dimensional tissue organization:The Perivascular niche

DAPIGFPCXCl12

Properties of brain tumor initiating cells within the perivascular nichetrophic support - Calabrese (2007) Cancer Cell

Increased DNA repair, ABC transporter expression - Bao (2006) Nature

CXCR4

Page 15: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Mutational activation of stromaMaffini et al.(2003) J Cell Sci 117:1495-1502

21 days old-remove epithelial cells from mammary glands52 days old-NMU or vehicle injection57 days old-NMU or vehicle treated EC transplant9 month experiment

NMU

Veh

EC transplant % tumors

76

75

0

0

Page 16: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Fibroblasts and driving oncogenesis

Normal fibroblasts

CAFs

NPE

Tag-HPE

NPE

Tag-HPE

No tumor

No tumor

No tumor

Malignant progression

Olumi AF et al (1999) Cancer Res. 59:5002

Page 17: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Stromal determinants of pediatric brain tumorigenesis

Page 18: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

brain tumor incidence

0

5

10

15

20

25

Age in years

Page 19: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Glioma formation in NF1

Page 20: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Optic pathway glioma formation in NF1

Nf1 +/- AstroNf1 +/- brain

Nf1 -/- AstroNf1 +/- brain

Nf1 -/- AstroNf1 +/+brain

9 months

Hyperplasia

98% OPGs

Hyperplasia

Bajenaru et al. (2003) Cancer Research 63:8573-8577 Nf1flox/flox or Nf1flox/- crossed or not with GFAP-Cre transgenic mice

Page 21: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Developmental regulation of CXCL12 expression in human brain

Warrington et al. (2007) Cancer Research

Page 22: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Multiple sources of CXCL12 are present in OPGCXCL12 neurofilament

CXCL12 CD68 pCXCR4

CXCL12 CXCL12

Warrington et al. (2007) Cancer Research

Page 23: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

CXCL12 stimulates Nf1-/- but not Nf1+/+ astrocyte growth in a cAMP dependent

manner

-40

-30

-20

-10

0

10

20Nf1+/+

Nf1-/-

CXCL12 + - + + - + FSK - + + - + +

CXCL12

Nf1+/+ Nf1-/-

-30

-20

-10

0

10

20

30Nf1+/+

Nf1-/-

DDA

Warrington et al. (2007) Cancer Research

Page 24: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Neurofibromin loss alters CXCR4-mediated cAMP responses

Warrington et al. (2007) Cancer Research

Page 25: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Mutational modulation of stromal response pathways: neurofibromin and CXCR4

R4R4

L12L12

GRKs

R4R4

L12L12

PP

arrestin

AC

ATP cAMPGi

NF

RAS

growthgrowth

Page 26: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Altering cAMP levels in the brain can alter the pattern of tumorigenesis in a mouse model of

NF1

Page 27: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Conclusions

Carcinogenesis is not always a cell autonomous event.

Abnormal epithelial-stromal interactions can promote tumorigenesis.

Stromal elements represent novel therapeutic targets

Page 28: Stromal Influences on Tumor Formation and Growth Joshua B Rubin, M.D., Ph.D. Department of Pediatrics Division of Pediatric Hematology/Oncology Washington

Thanks to

Washington University

Nicole WarringtonB. Mark WoernerLihua YangErin GribbenMahil RaoShyam Rao

David GutmannArie PerryErin JacksonDavid Piwnica-Worms