Expression of Akt Kinase-Interacting Protein 1, a Scaffold Protein of the PI3K/PDK1/Akt Pathway, in Pancreatic Cancer

被引:10
作者
Ohtsubo, Koushiro [1 ]
Yamada, Tadaaki [1 ]
Zhao, Lu [1 ]
Jin, Tie-Feng [1 ]
Takeuchi, Shinji [1 ]
Mouri, Hisatsugu [1 ]
Yamashita, Kaname [1 ]
Yasumoto, Kazuo [1 ]
Fujita, Naoya [2 ]
Kitagawa, Hirohisa [3 ]
Ohta, Tetsuo [3 ]
Ikeda, Hiroko [4 ]
Yano, Seiji [1 ]
机构
[1] Kanazawa Univ, Canc Res Inst, Div Med Oncol, Kanazawa, Ishikawa 9200934, Japan
[2] Japanese Fdn Canc Res, Div Canc Chemotherapy Ctr, Tokyo, Japan
[3] Kanazawa Univ, Dept Surg Gastroenterol, Kanazawa, Ishikawa 9200934, Japan
[4] Kanazawa Univ, Div Pathol, Kanazawa, Ishikawa 9200934, Japan
基金
日本学术振兴会;
关键词
Akt kinase-interacting protein 1; scaffold protein; PI3K/PDK1/Akt pathway; pancreatic cancer; CARCINOMA CELLS; PHASE-III; IN-VIVO; AMG; 479; GEMCITABINE; GROWTH; EPIDEMIOLOGY; INHIBITION; MUTATIONS; APOPTOSIS;
D O I
10.1097/MPA.0000000000000168
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objectives: Akt kinase-interacting protein 1 (Aki1) has been reported to be a scaffold protein of the PI3K (phosphoinositide 3-kinase)/PDK1 (3-phosphoinositide-dependent protein kinase)/Akt pathway and to interact with epidermal growth factor receptor signaling. Although Aki1 has been reported to be expressed in lung cancer, the significance of its expression in pancreatic cancer has not been clarified. Methods: The expression of Aki1 and its associated proteins was assayed in pancreatic cancer cell lines, and its involvement in cell viability was examined by treatment with Aki1 small interfering RNA. We also assessed the immunohistochemical expression of Aki1 in tissue samples from 60 patients with pancreatic cancer. Results: All of the pancreatic cancer cell lines expressed Aki1 and its associated proteins at various levels. Treatment with Aki1 small interfering RNA or PI3K inhibitor inhibited the viability of Panc1 cells. Silencing of Aki1 in Panc1 cells reduced the phosphorylation of Akt and increased the phosphorylation of cleaved PARP. The Aki1 was expressed in 25 (42%) of the 60 pancreatic cancers, but there was no correlation between Aki1 expression and clinicopathologic parameters. We observed a statistically significant correlation between Aki1 and p-Akt expression (P = 0.016). Conclusions: Inhibition of the Aki1-Akt axis may be a therapeutic target in some patients with pancreatic cancer.
引用
收藏
页码:1093 / 1100
页数:8
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