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Review
. 2017 Jun 15;77(12):3135-3139.
doi: 10.1158/0008-5472.CAN-16-3566. Epub 2017 Jun 5.

FOXM1 in Cancer: Interactions and Vulnerabilities

Affiliations
Review

FOXM1 in Cancer: Interactions and Vulnerabilities

Andrei L Gartel. Cancer Res. .

Abstract

FOXM1 is a transcription factor of the Forkhead family that is required for cell proliferation of normal cells. However, FOXM1 is repeatedly overexpressed in a variety of human cancers, and it has been implicated in all major hallmarks of cancer delineated by Hanahan and Weinberg. It has been postulated that the oncogenic potential of FOXM1 is determined by its capacity to transactivate target genes that are implicated in different phases of cancer development. However, FOXM1 may also play an oncogenic role by interacting with other proteins, such as β-catenin or SMAD3 to induce oncogenic WNT and TGFβ signaling pathways, respectively. In this review, I will discuss the protein-protein interactions of FOXM1 that are critical for cancer development and may represent novel targets for anticancer drugs. Cancer Res; 77(12); 3135-9. ©2017 AACR.

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Conflict of interest statement

Conflict of interest: The author declared no conflict of interest.

Figures

Figure 1
Figure 1
Different examples of FOXM1 interactions in cancer. (A) Several proteins stabilize FOXM1 and increase its oncogenic activity. (B) FOXM1 as an assembly factor contributes to Wnt and TGFβ signaling. (C) Proteotoxic stress suppresses FOXM1 via up-regulation of HSP70 and its interaction with FOXM1.

References

    1. Laoukili J, Stahl M, Medema RH. FoxM1: At the crossroads of ageing and cancer. Biochim Biophys Acta. 2007;1775:92–102. - PubMed
    1. Pilarsky C, Wenzig M, Specht T, Saeger HD, Grutzmann R. Identification and validation of commonly overexpressed genes in solid tumors by comparison of microarray data. Neoplasia. 2004;6:744–50. - PMC - PubMed
    1. Halasi M, Gartel AL. FOX(M1) News--It Is Cancer. Mol Cancer Ther. 2013;12:245–54. - PMC - PubMed
    1. Hanahan D, Weinberg RA. Hallmarks of cancer: the next generation. Cell. 2011;144:646–74. - PubMed
    1. Bhat UG, Jagadeeswaran R, Halasi M, Gartel AL. Nucleophosmin interacts with FOXM1 and modulates the level and localization of FOXM1 in human cancer cells. J Biol Chem. 2011;286:41425–33. - PMC - PubMed

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