TY - JOUR
T1 - An actin-binding protein girdin regulates the motility of breast cancer cells
AU - Jiang, Ping
AU - Enomoto, Atsushi
AU - Jijiwa, Mayumi
AU - Kato, Takuya
AU - Hasegawa, Taisaku
AU - Ishida, Maki
AU - Sato, Tomoko
AU - Asai, Naoya
AU - Murakumo, Yoshiki
AU - Takahashi, Masahide
PY - 2008/3/1
Y1 - 2008/3/1
N2 - Girdin (girders of actin filaments) is a novel actin-binding Akt substrate that plays an important role in actin organization and Akt-dependent cell motility in fibroblasts. Here, we find that Girdin is expressed in a variety of cancer cell lines, including the breast cancer cell line MDA-MB-231, and is phosphorylated by the stimulation of insulin-like growth factor (IGF-I). In vitro migration and invasion assays showed that Girdin is required for the IGF-I-dependent cell movement of MDA-MB-231 cells. Short hairpin interfering RNA directed against Girdin markedly inhibited the metastasis of s.c. transplanted MDA-MB-231 cells in nude mice. In addition, Girdin is highly expressed in a variety of human malignant tissues, including breast, colon, lung, and uterine cervical carcinomas. These findings highlight the important role of Girdin in tumor progression in which the Akt signaling pathway is aberrantly activated.
AB - Girdin (girders of actin filaments) is a novel actin-binding Akt substrate that plays an important role in actin organization and Akt-dependent cell motility in fibroblasts. Here, we find that Girdin is expressed in a variety of cancer cell lines, including the breast cancer cell line MDA-MB-231, and is phosphorylated by the stimulation of insulin-like growth factor (IGF-I). In vitro migration and invasion assays showed that Girdin is required for the IGF-I-dependent cell movement of MDA-MB-231 cells. Short hairpin interfering RNA directed against Girdin markedly inhibited the metastasis of s.c. transplanted MDA-MB-231 cells in nude mice. In addition, Girdin is highly expressed in a variety of human malignant tissues, including breast, colon, lung, and uterine cervical carcinomas. These findings highlight the important role of Girdin in tumor progression in which the Akt signaling pathway is aberrantly activated.
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U2 - 10.1158/0008-5472.CAN-07-5111
DO - 10.1158/0008-5472.CAN-07-5111
M3 - Article
C2 - 18316593
AN - SCOPUS:40449105942
SN - 0008-5472
VL - 68
SP - 1310
EP - 1318
JO - Cancer Research
JF - Cancer Research
IS - 5
ER -