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651.O1.6 Genetic Events and Myeloma Pathogenesis

Monday, December 8, 2008: 1:30 PM-3:00 PM
Halls B and C (Moscone Center)
Moderators:
Selina Chen-Kiang, PhD and Ralph D. Sanderson
1:30 PM
A Novel Mechanism for Intrachromosomal Gene Amplification in Multiple Myeloma: 1q12 Pericentromeric Heterochromatin Mediates Breakage-Fusion-Bridge Cycles of the 1q12~23 Amplicon

Jeffrey Sawyer1*, Erming Tian2*, Edward Thomas1*, Mark Koller1*, Collin Stangeby1*, Gael Sammartino1*, Linda Goosen1*, Charles Swanson1*, Regina Lichti Binz1*, Bart Barlogie2* and John Shaughnessy2

1Pathology, University of Arkansas for Medical Sciences, Little Rock, AR
2Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR

1:45 PM
A Comparative Oncogenomic Analysis Identifies Genetic Events Associated with Myeloma Progression and Drug Resistance

Marta Chesi, PhD*, Esteban Braggio*, Jonathan J Keats* and P. Leif Bergsagel, MD

Comprehensive Cancer Center, Mayo Clinic, Scottsdale, AZ

2:00 PM
Characterization of Cancer Stem Cells in Multiple Myeloma

Haiming Chen, MD, PhD1*, Mingjie Li1*, Eric Sanchez1*, Cathy S Wang1*, Ariana M Berenson1*, Jennifer Li1*, Jeffrey A Steinberg1*, James Wang1*, Jing Shen1*, Zhi-Wei Li, PhD1, Benjamin Bonavida, PhD2 and James R. Berenson, MD1

1Hematology/Oncology, Institute for Myeloma & Bone Cancer Research, West Hollywood, CA
2Microbiology, Immunology & Molecular Genetics, University of CA, Los Angeles, Los Angeles, CA

2:15 PM
The Impact of Constitutional Copy Number Variants in Myeloma

Matthew W Jenner1*, David C Johnson2*, Paola E Leone2*, Brian A Walker3*, David Gonzalez2*, Nicholas J Dickens2*, Faith E Davies2 and Gareth J. Morgan2

1Section of Haemato-Oncology, Institute of Cancer Research, London, United Kingdom
2Section of Haemato-Oncology, Institute of Cancer Research, Sutton, United Kingdom
3Section of Haemato-Oncology, The Institute of Cancer Research, London, United Kingdom

2:30 PM
Interim Analyses of the MMRC Reference Collection Identifies Recurrent Genomic-Level Events in Multiple Myeloma and Demonstrates That CDKN2C/p18 Deletion Is the Pre-Eminent Copy Number Alteration in Poor Prognosis Disease

Michael A Chapman1*, Jean-Philippe Brunet1*, Angela Baker2*, Jonathan Keats3, Gregory Ahmann, BS3, Anna C Schinzel, PhD4*, Anna Moore2*, Vijayalakshmi Shanmugam2*, Louise M. Perkins, PhD5, Daniel Auclair, PhD5*, William C. Hahn, M.D., Ph.D4*, P. Leif Bergsagel, MD3, Rafael Fonseca, MD3, John Carpten2*, Jeffrey Trent6* and Todd R. Golub, MD4

1Cancer Program, Broad Institute, Cambridge, MA
2Integrated Cancer Genomics Division, Translational Genomics Research Institute, Phoenix, AZ
3Mayo Clinic Arizona, Scottsdale, AZ
4Dana-Farber Cancer Institute, Boston, MA
5Multiple Myeloma Research Foundation, Norwalk, CT
6Genetic Basis of Human Disease Division, Translational Genomics Research Institute, Phoenix, AZ

2:45 PM
Alternate Splicing Is a Frequent Event and Impacts Clinical Outcome in Myeloma: A High-Density Exon Array Analysis of Uniformly Treated Newly-Diagnosed Myeloma Patients

Nikhil C. Munshi, MD1, Cheng Li, PhD2*, Stephane Minvielle, PhD3*, Samir B Amin, MBBS4*, Philippe Moreau, MD3*, Florence Magrangeas3*, Kenneth C Anderson, MD4* and Herve Avet-Loiseau, MD3*

1Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston VA Cancer Healthcare System, Boston, MA
2Department of Biostatistics and Department of Biostatistics and Computational Biology, Harvard School of Public Health and Dana-Farber Cancer Institute, Boston
3Hematology Department, Hopital de Nantes, Nantes, France
4Jerome Lipper Multiple Myeloma Disease Center, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA

*signifies non-member of ASH