Insulin-IGF signaling affects cell transformation in the BALB/c 3T3 cell model

被引:8
作者
Poburski, Doerte [1 ]
Leovsky, Christiane [1 ]
Boerner, Josefine Barbara [1 ]
Szimmtenings, Luisa [1 ]
Ristow, Michael [1 ,2 ]
Glei, Michael [1 ]
Thierbach, Rene [1 ]
机构
[1] Friedrich Schiller Univ Jena, Inst Nutr, Dornburger Str 24, D-07743 Jena, Germany
[2] Swiss Fed Inst Technol, Energy Metab Lab, Schorenstr 16, CH-8603 Schwerzenbach, Switzerland
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
关键词
GROWTH-FACTOR RECEPTOR; I RECEPTOR; INHIBITOR OSI-906; DUAL INHIBITOR; BREAST-CANCER; RAS-ERK; PATHWAY; EXPRESSION; CARCINOMA; TARGET;
D O I
10.1038/srep37120
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The increased cancer mortality of diabetes type 2 patients is most likely an evidence of the tight connection between tumor development and energy metabolism. A major focus of today's research is still the identification of key proteins of both diseases and the development of corresponding inhibitors. In this study we combined the two-stage BALB/c-3T3 cell transformation assay (BALB-CTA) with the IR/IGF-1R inhibitor OSI-906 (linsitinib) and analyzed alterations in protein activity and energy parameters in non-transformed as well as transformed cells. OSI-906 successfully inhibited the phosphorylation of IR/IGF-1R and decreased cell growth in non-transformed cells. In the BALB-CTA, a permanent treatment with OSI-906 reduced cellular transformation dose-dependently, whereas a temporary treatment gave evidence for a preventive effect in the promotion phase. Furthermore, even though several key proteins were affected, it was possible to show that the phosphorylation of GSK3, Erk 1/2 and the S6 protein are not crucial for the cell foci reducing effect of OSI-906. Taken together, the BALB-CTA confirmed results of OSI-906 from animal studies and enhanced the knowledge of its mode of action. Therefore, the BALB-CTA offers the opportunity to analyze alterations in the transformation process more precisely and will be helpful to identify effective cancer treatments.
引用
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页数:12
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