ERBB family receptor tyrosine kinases are overexpressed in a significant su
bset of breast cancers. One of these receptors, HER2/neu, or ErbB-2, is the
target for a new rational therapeutic antibody, Herceptin. Other inhibitor
s that target this receptor, and another family member, the epidermal growt
h factor (EGF) receptor, are moving into clinical trials. Both of these rec
eptors are sometimes overexpressed in breast cancer, and still subject to r
egulation by hormones and other physiological regulators. Optimal use of th
erapeutics targeting these receptors will require consideration of the seve
ral modes of regulation of these receptors and their interactions with ster
oid receptors.