癌变
转录因子
转移
癌症研究
肿瘤进展
癌症
生物
抑制器
PI3K/AKT/mTOR通路
乳腺癌
信号转导
细胞生物学
基因
遗传学
作者
Marten Hornsveld,Lydia M.M. Smits,Maaike Meerlo,Miranda van Amersfoort,Marian J.A. Groot Koerkamp,Dik van Leenen,David E.A. Kloet,Frank C. P. Holstege,Patrick W.B. Derksen,Boudewijn Burgering,Tobias B. Dansen
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2018-02-13
卷期号:78 (9): 2356-2369
被引量:90
标识
DOI:10.1158/0008-5472.can-17-2511
摘要
Abstract FOXO transcription factors are regulators of cellular homeostasis and putative tumor suppressors, yet the role of FOXO in cancer progression remains to be determined. The data on FOXO function, particularly for epithelial cancers, are fragmentary and come from studies that focused on isolated aspects of cancer. To clarify the role of FOXO in epithelial cancer progression, we characterized the effects of inducible FOXO activation and loss in a mouse model of metastatic invasive lobular carcinoma. Strikingly, either activation or loss of FOXO function suppressed tumor growth and metastasis. We show that the multitude of cellular processes critically affected by FOXO function include proliferation, survival, redox homeostasis, and PI3K signaling, all of which must be carefully balanced for tumor cells to thrive. Significance: FOXO proteins are not solely tumor suppressors, but also support tumor growth and metastasis by regulating a multitude of cellular processes essential for tumorigenesis. Cancer Res; 78(9); 2356–69. ©2018 AACR.
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