atm , ataxia telangiectasia , & cancer

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ATM, Ataxia Telangiectasia, & Cancer

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ATM , Ataxia Telangiectasia , & Cancer. Ataxia Telangiectasia. Characterized by: Cerebellar deterioration Oculocutaneous telangiectasia Immunodeficiency Genomic Instability Acute sensitivity to ionizing radiation Predisposition to malignancy. - PowerPoint PPT Presentation

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Page 1: ATM , Ataxia Telangiectasia , & Cancer

ATM,

Ataxia Telangiectasia, & Cancer

Page 2: ATM , Ataxia Telangiectasia , & Cancer

Ataxia Telangiectasia

Characterized by:• Cerebellar deterioration• Oculocutaneous telangiectasia • Immunodeficiency• Genomic Instability• Acute sensitivity to ionizing

radiation• Predisposition to malignancy

Page 3: ATM , Ataxia Telangiectasia , & Cancer

The ATM gene was discovered by positional cloning

• Chromosome 11q22• 150kb• 66 exons

Savitsky et. al. “A Single Ataxia Telangiectasia Gene with a Product Similar to PI-3 Kinase”

Page 4: ATM , Ataxia Telangiectasia , & Cancer

ATM is a serine/threonine kinase

• PI3K-related protein kinase family (a.k.a. PIKK)• Present in undamaged cell nuclei in inactive state• In response to DNA damage, becomes active and

phosphorylates multiple substrates

Page 5: ATM , Ataxia Telangiectasia , & Cancer

Cellular Response to DNA Damage

Page 6: ATM , Ataxia Telangiectasia , & Cancer

G1/S checkpoint

ATM

p53

P

CHK2

P

P

MDM2

P

p21 CDK2 G1ARREST

Page 7: ATM , Ataxia Telangiectasia , & Cancer

G1/S and G2/M Checkpoints

ATM

CHK1 CHK2

P P

CDC25AP P

Degradation and Cell Cycle Arrest

Page 8: ATM , Ataxia Telangiectasia , & Cancer

ATM mediated activation of BRCA1 following DNA Damage

ATM

BRCA1

CHK2

P

P

PCtIP

P

DNA REPAIR

Page 9: ATM , Ataxia Telangiectasia , & Cancer

ATM

H2AX

P

Congregates at site of DSB and recruits repair factors such asthe MRN complex, BRCA 1, and RAD 51

Page 10: ATM , Ataxia Telangiectasia , & Cancer

ATM and Telomere maintenance

A-T cells display abnormally shortened telomeres, abnormal association of chromosome ends, and telomere clustering

Page 11: ATM , Ataxia Telangiectasia , & Cancer

Animal Model of A-T

Barlow et. al. “Atm-Deficient Mice: A Paradigm of Ataxia Telangiectasia”

Page 12: ATM , Ataxia Telangiectasia , & Cancer

Heterozygous Carriersof a mutated ATM gene

• The belief that heterozygous carriers are predisposed to malignancy is controversial

• Point mutations can have dominant negative effect

Page 13: ATM , Ataxia Telangiectasia , & Cancer

Current Treatments for A-T

• No gene therapy or A-T specific treatment exists • Symptomatic (such as neurorehabilitation)• Routine screenings for malignancies• Gamma-globulin injections

• Iron chelator therapy?

Page 14: ATM , Ataxia Telangiectasia , & Cancer

Sources• Shiloh, Yosef. "ATM and Related Protein Kinases: Safeguarding Genome Integrity." Nature Reviews: Cancer 3

(2003): 155-168. • McKinnon, Peter. "ATM and Ataxia Telangiectasia." EMBO Reports 5 (2004): 772-776. • Barlow, Et. Al.. "Atm-Deficient Mice: A Paradigm of Ataxia Telangiectasia." Cell 86.1 (1996): 159-171.• Savitsky, Et. Al.. "A Single Ataxia Telangiectasia Gene with a Product Similar to PI-3 Kinase." Science 268

(1995): 1749-1753. • Thompson, Et. Al.. "Cancer Risks and Mortality in Heterozygous ATM Mutation Carriers." Journal of the National

Cancer Institute 97 (2005): 813-822. • Lu, Shu, and Kate Shen. "Atm-haploinsufficiency Enhances Susceptibility to Carcinogen-induced Mammary

Tumors." Carcinogenesis 27 (2006): 848-855. • Scott, Et. Al.. "Missense Mutations but Not Allelic Variants Alter the Function of ATM by Dominant Interference in

Patients with Breast Cancer." PNAS 99.2 (2002): 925-930. • Uhrhammer N, Bay JO, Perlman S, Gatti RA . Ataxia-Telangiectasia and variants. Atlas Genet Cytogenet Oncol

Haematol. April 2002 .URL : http://AtlasGeneticsOncology.org/Deep/ATMID20006.html

• Shackelford, Et. Al.. "Iron Chelators Increase the Resistance of Ataxia Telangeictasia Cells to Oxidative Stress." DNA Repair 3.10 (2004): 1263-1272.

• Online Mendelian Inheritance in Man: ATM Gene. Ada Hamosh. 19 July 2007. Johns Hopkins University, Baltimore, MD. 7 Mar. 2008 <http://www.ncbi.nlm.nih.gov.libproxy.lib.unc.edu/entrez/dispomim.cgi?id=607585>.