TY - JOUR
T1 - Expression and regulatory role of GAIP-interacting protein GIPC in pancreatic adenocarcinoma
AU - Muders, Michael H.
AU - Dutta, Shamit K.
AU - Wang, Ling
AU - Lau, Julie S.
AU - Bhattacharya, Resham
AU - Smyrk, Thomas C.
AU - Chari, Suresh T.
AU - Datta, Kaustubh
AU - Mukhopadhyay, Debabrata
PY - 2006/11/1
Y1 - 2006/11/1
N2 - Regulator of G-protein signaling-GAIP-interacting protein COOH terminus (GIPC) is involved in protein trafficking, endocytosis, and receptor clustering and is associated with insulin-like growth factor I receptor (IGF-IR), a receptor important for proliferation and anchorage-independent growth. Here, we described GIPC expression in different human pancreatic adenocarcinoma (PCA) cell lines and we examined the role of GIPC in the regulation of IGF-IR protein levels in PCA. Interestingly, inhibition of GIPC expression by RNA interference led to reduced IGF-IR protein levels and a subsequent decrease in proliferation of PCA cells. We also determined that the PDZ domain of GIPC is essential for the post-translational regulation and the binding of IGF-IR. The importance of GIPC in pancreatic cancer development and progression is supported by tissue microarray data of 300 pancreatic cancer specimens where GIPC is highly expressed in PCA. Taken together, our data suggest that GIPC is a central molecule for the stability of IGF-IR and could be a target for future therapy.
AB - Regulator of G-protein signaling-GAIP-interacting protein COOH terminus (GIPC) is involved in protein trafficking, endocytosis, and receptor clustering and is associated with insulin-like growth factor I receptor (IGF-IR), a receptor important for proliferation and anchorage-independent growth. Here, we described GIPC expression in different human pancreatic adenocarcinoma (PCA) cell lines and we examined the role of GIPC in the regulation of IGF-IR protein levels in PCA. Interestingly, inhibition of GIPC expression by RNA interference led to reduced IGF-IR protein levels and a subsequent decrease in proliferation of PCA cells. We also determined that the PDZ domain of GIPC is essential for the post-translational regulation and the binding of IGF-IR. The importance of GIPC in pancreatic cancer development and progression is supported by tissue microarray data of 300 pancreatic cancer specimens where GIPC is highly expressed in PCA. Taken together, our data suggest that GIPC is a central molecule for the stability of IGF-IR and could be a target for future therapy.
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U2 - 10.1158/0008-5472.CAN-06-2321
DO - 10.1158/0008-5472.CAN-06-2321
M3 - Article
C2 - 17079444
AN - SCOPUS:33751287963
SN - 0008-5472
VL - 66
SP - 10264
EP - 10268
JO - Cancer Research
JF - Cancer Research
IS - 21
ER -