fullofbeans
11-07-2011, 05:45 PM
Good summary of the response rates of various combinations for anti Her:
http://www.nature.com/nrc/journal/v9/n7/fig_tab/nrc2656_T3.html
And a very good full article:
http://www.nature.com/nrc/journal/v9/n7/full/nrc2656.html
Novel anticancer targets: revisiting ERBB2 and discovering ERBB3
José Baselga1 (http://www.nature.com/nrc/journal/v9/n7/full/nrc2656.html#a1) & Sandra M. Swain2 (http://www.nature.com/nrc/journal/v9/n7/full/nrc2656.html#a2) About the authors (http://www.nature.com/nrc/journal/v9/n7/authors/nrc2656.html)
Top of page (http://www.nature.com/nrc/journal/v9/n7/full/nrc2656.html#top)Abstract
Aberrant receptor expression or functioning of the epidermal growth factor receptor (Erbb) family plays a crucial part in the development and evolution of cancer. Inhibiting the signalling activity of individual receptors in this family has advanced the treatment of a range of human cancers. In this Review we re-evaluate the role of two important family members, ERBB2 (also known as HER2) and ERBB3 (also known as HER3), and explore the mechanisms of action and preclinical and clinical data for new therapies that target signalling through these pivotal receptors. These new therapies include tyrosine kinase inhibitors, antibody–chemotherapy conjugates, heat-shock protein inhibitors and antibodies that interfere with the formation of ERBB2–ERBB3 dimers.
We want the magic combo to be discovered.
http://www.nature.com/nrc/journal/v9/n7/fig_tab/nrc2656_T3.html
And a very good full article:
http://www.nature.com/nrc/journal/v9/n7/full/nrc2656.html
Novel anticancer targets: revisiting ERBB2 and discovering ERBB3
José Baselga1 (http://www.nature.com/nrc/journal/v9/n7/full/nrc2656.html#a1) & Sandra M. Swain2 (http://www.nature.com/nrc/journal/v9/n7/full/nrc2656.html#a2) About the authors (http://www.nature.com/nrc/journal/v9/n7/authors/nrc2656.html)
Top of page (http://www.nature.com/nrc/journal/v9/n7/full/nrc2656.html#top)Abstract
Aberrant receptor expression or functioning of the epidermal growth factor receptor (Erbb) family plays a crucial part in the development and evolution of cancer. Inhibiting the signalling activity of individual receptors in this family has advanced the treatment of a range of human cancers. In this Review we re-evaluate the role of two important family members, ERBB2 (also known as HER2) and ERBB3 (also known as HER3), and explore the mechanisms of action and preclinical and clinical data for new therapies that target signalling through these pivotal receptors. These new therapies include tyrosine kinase inhibitors, antibody–chemotherapy conjugates, heat-shock protein inhibitors and antibodies that interfere with the formation of ERBB2–ERBB3 dimers.
We want the magic combo to be discovered.