OBJECTIVES. 1. List the major hallmarks of cancer. 2. Relate specific genes/proteins to individual hallmarks

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OBJECTIVES 1. List the major hallmarks of cancer 2. Relate specific genes/proteins to individual hallmarks 3. Explain how hallmarks of cancer lead to cancer development

Case Study 60 year old female Previously treated for breast cancer (5 years prior); no recurrence Presents with persistent cough, shortness of breath, famgue X- ray reveals small mass in lep lung Source: www.123rf.com A biopsy is performed

think- discuss- share A physician meets with this pament. What is the first quesmon she asks about the pament s lifestyle?

www.lung.org

www.lung.org

brainstorming A pathologist analyzes the biopsy sample. What does she look for?, i.e. What informamon is gained from the analysis of the biopsy?

www.lung.org TYPES OF LUNG CANCER

Biopsy results indicate that pahent has a metastahc tumor of breast cancer origin in lung. Tumor is a carcinoma.

QUESTION What changes occurred to a breast epithelial cell that led to the formahon of a metastahc tumor in the lung? Biopsy results indicate that pahent has a metastahc tumor of breast cancer origin in lung. Tumor is a carcinoma.

Douglas Hanahan Robert Weinberg

Hanahan and Weinberg (2000) Cell, 100: 57 70.

GROWTH FACTOR (GF) RECEPTOR INTRACELLULAR SIGNALING PATHWAY CELL DIVISION

GROWTH FACTOR (GF) RECEPTOR Ras INTRACELLULAR SIGNALING PATHWAY CELL DIVISION

RECEPTOR Hyperac(ve Mutant Ras in Cancers Ras INTRACELLULAR SIGNALING PATHWAY CELL DIVISION

GROWTH FACTOR (GF) Amplified EGF Receptors in Cancer INTRACELLULAR SIGNALING PATHWAY CELL DIVISION

CLASSES OF LUNG ADENOCARCINOMA Ras Source: Cheng, L. et al. (2012) Modern Pathology, 25: 347 369.

TARCEVA A DRUG WHICH TARGETS EGF RECEPTOR IN LUNG CANCER www.lifewithlungcancer.org www.tarceva.com

Hanahan and Weinberg (2000) Cell, 100: 57 70.

EUKARYOTIC CELL CYCLE

RECEPTOR INTRACELLULAR SIGNALING PATHWAY Rb G 0

GROWTH FACTOR (GF) RECEPTOR INTRACELLULAR SIGNALING PATHWAY Modified and Inac(ve Rb Rb- P CELL DIVISION

RECEPTOR INTRACELLULAR SIGNALING PATHWAY Rb Inac(ve Mutant Rb in Cancer CELL DIVISION

p53 s NORMAL ROLE IS TO INHIBIT CELL DIVISION IN RESPONSE TO CELLULAR STRESSES LIKE DNA DAMAGE

TUMOR CELLS LACKING p53 DO NOT ARREST CELL CYCLE Source: Molecular Biology of the Cell, Alberts et al.

Hanahan and Weinberg (2000) Cell, 100: 57 70.

APOPTOSIS PROGRAMMED CELL DEATH Source: Molecular Biology of the Cell, Alberts et al.

INSULIN- LIKE GROWTH FACTOR (IGF- 1) IGF- 1R Ras INTRACELLULAR SIGNALING PATHWAY CELL SURVIVAL CELL DIVISION

INSULIN- LIKE GROWTH FACTOR (IGF- 1) IGF- 1R Ras INTRACELLULAR SIGNALING PATHWAY CELL SURVIVAL CELL DIVISION SOME CANCER CELLS UPREGULATE CELL SURVIVAL PATHWAYS TO EVADE APOPTOSIS

Hanahan and Weinberg (2000) Cell, 100: 57 70.

TELOMERES ARE CHROMOSOME ENDS TELOMERES ARE MADE BY TELOMERASE EARLY IN DEVELOPMENT; THEN TELOMERASE ACTIVITY IS NORMALLY TURNED OFF TELOMERES SHORTEN WITH EACH CELL DIVISION, ULTIMATELY LEADING TO SENESCENCE

CANCER CELLS REACTIVATE TELOMERASE

Biopsy results indicate that pahent has a metastahc tumor of breast cancer origin in lung. Tumor is a carcinoma.

Hanahan and Weinberg (2000) Cell, 100: 57 70.

The formahon of new blood vessels from pre- exishng blood vessels.

VEGF = Vascular Endothelial Growth Factor

Biopsy results indicate that pahent has a metastahc tumor of breast cancer origin in lung. Tumor is a carcinoma.

Hanahan and Weinberg (2000) Cell, 100: 57 70.

PRIMARY BREAST CARCINOMA METASTATIC TUMOR IN LUNG

METASTASIS CELLS OF PRIMARY TUMOR REDUCE EXPRESSION OF INTERCELLULAR CONNECTIONS (E- CADHERINS) AND CONNECTIONS TO THE EXTRACELLULAR MATRIX (INTEGRINS) TO ALLOW METASTASIS

CANCER DEVELOPMENT IS A MULTI- STEP PROCESS. INDIVIDUAL STEPS CAN OCCUR IS DIFFERENT ORDER. Hanahan and Weinberg (2000) Cell, 100: 57 70.

THE HALLMARKS OF CANCER Ras, EGF Receptor Rb, p53 IGF Telomerase VEGF E- cadherin

You should be able to... 1. List the major hallmarks of cancer 2. Relate specific genes/proteins to individual hallmarks 3. Explain how hallmarks of cancer lead to cancer development