I got my Christmas Wish!!!!!!!!!!!!!!!!!
-----Original Message-----
From: Slingluff, Craig *HS [mailto:CLS8H@hscmail.mcc.virginia.edu]
Sent: Thursday, December 24, 2009 11:51 AM
To: dbreitfe@rochester.rr.com
Cc: Weber, Michael J - Cancer Center *HS; Engelhard, Victor H
Subject: RE: Identification and Validation of Combination Therapies for Melanomas
Dear Mr. Breitfeller,
Mike Weber was kind to forward your paper and email. It appears that you have a very good sense of, and interest in, the immune response to melanoma and to cancer in general. I believe you are right that timing of the various components of the immune response, especially with combination therapies, is important, just as it is in the orchestration of a beautiful symphony. I wish you success in your treatments and in your work to understand and to explain the immune response to cancer.
Craig Slingluff
Craig L. Slingluff, Jr. M.D.
Joseph Helms Farrow Professor of Surgery
Division of Surgical Oncology
Vice-Chair for Research
Director, Human Immune Therapy Center
University of Virginia
Charlottesville, VA 22908
cls8h@virginia.edu
434-924-1730
http://www.box.net/shared/kjgr6dkztj
Melanoma and the Magic Bullet (monoclonal Antibodies)
Michael J. Weber, Ph.D.
Professor of Microbiology
Research Interests:
Signal Transducing Kinases in Cancer
Signal transduction by serine/threonine kinases
The Weber laboratory utilizes tools of cell biology, protein chemistry and molecular biology to understand how signal transduction pathways control cell growth and apoptosis and how these controls are altered in cancer. A major focus of this research is on the MAP Kinase cascade, a ubiquitous signaling pathway that generates specific biological outcomes dependent on biological context. Recent findings of the lab have demonstrated an important role for "scaffolding proteins" that assemble components of the signaling cascades. They recently discovered the MORG1 scaffold protein (MAP Kinase Organizer) that regulates responses to LPA but not EGF. Signaling scaffolds can control the location, regulation, timing, substrates, biological functions, and suitability for therapeutic intervention of a signaling pathway. This research made use of the Biostatistics Core, to help evaluate multi-factorial responses to mitogens, and the Mass Spec and DNA cores for molecular and proteomic analysis.
The lab pioneered the use of phosphorylation-site specific antibodies to probe archival paraffin-embedded pathology specimens, and discovered that the MAP Kinase cascade was activated in prostate cancer. Activation of this pathway is sufficient for and can be necessary for progression of prostate cancer to an androgen-independent disease. Therefore the Ras-MAP Kinase pathway is an attractive target for therapy of advanced prostate cancer.
Current research aims to determine how to select combinations of therapies in cancer treatment.
Merry Christmas
Jimmy Breitfeller
Take Care,
Jimmy B
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