TY - JOUR
T1 - Clinicopathological significance of growth factors and their receptors as potential therapeutic targets for biliary tract carcinoma
AU - Ojima, Hidenori
PY - 2012/7
Y1 - 2012/7
N2 - Biliary tract carcinoma (BTC) has a poor prognosis. However, no standard chemotherapy regimens have been established for inoperable cases or cases of recurrence after surgical resection. Recent molecular biological analysis has shown that epidermal growth factor receptor, human epidermal growth factor receptor 2, vascular endothelial growth factor, hepatocyte growth factor, c-Met and transforming growth factor-beta could be potential targets for therapy of BTC. It is considered that these molecules are involved in the carcinogenesis, invasion, and progression of BTC. Furthermore, immunohistochemical overexpression of these targets is associated with several clinicopathological factors. This article reviews the clinicopathological significance of these growth factors and their receptors.
AB - Biliary tract carcinoma (BTC) has a poor prognosis. However, no standard chemotherapy regimens have been established for inoperable cases or cases of recurrence after surgical resection. Recent molecular biological analysis has shown that epidermal growth factor receptor, human epidermal growth factor receptor 2, vascular endothelial growth factor, hepatocyte growth factor, c-Met and transforming growth factor-beta could be potential targets for therapy of BTC. It is considered that these molecules are involved in the carcinogenesis, invasion, and progression of BTC. Furthermore, immunohistochemical overexpression of these targets is associated with several clinicopathological factors. This article reviews the clinicopathological significance of these growth factors and their receptors.
KW - Biliary tract carcinoma
KW - Chemotherapy
KW - Growth factor receptor
KW - Immunohistochemistry
KW - Molecular target
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U2 - 10.1007/s00534-011-0497-z
DO - 10.1007/s00534-011-0497-z
M3 - Review article
C2 - 22278347
AN - SCOPUS:84867396347
SN - 1868-6974
VL - 19
SP - 319
EP - 325
JO - Journal of Hepato-Biliary-Pancreatic Sciences
JF - Journal of Hepato-Biliary-Pancreatic Sciences
IS - 4
ER -