β-catenin confers resistance to PI3K and AKT inhibitors and subverts FOXO3a to promote metastasis in colon cancer - PubMed (original) (raw)
. 2012 Jun;18(6):892-901.
doi: 10.1038/nm.2772.
Paloma Ordóñez-Morán, Isabel Puig, Irene Chicote, Oriol Arqués, Stefania Landolfi, Yolanda Fernández, José Raúl Herance, Juan D Gispert, Leire Mendizabal, Susana Aguilar, Santiago Ramón y Cajal, Simó Schwartz Jr, Ana Vivancos, Eloy Espín, Santiago Rojas, José Baselga, Josep Tabernero, Alberto Muñoz, Héctor G Palmer
Affiliations
- PMID: 22610277
- DOI: 10.1038/nm.2772
Free article
β-catenin confers resistance to PI3K and AKT inhibitors and subverts FOXO3a to promote metastasis in colon cancer
Stephan P Tenbaum et al. Nat Med. 2012 Jun.
Free article
Abstract
The Wnt–β-catenin and PI3K-AKT-FOXO3a pathways have a central role in cancer. AKT phosporylates FOXO3a, relocating it from the cell nucleus to the cytoplasm, an effect that is reversed by PI3K and AKT inhibitors. Simultaneous hyperactivation of the Wnt–β-catenin pathway and inhibition of PI3K-AKT signaling promote nuclear accumulation of β-catenin and FOXO3a, respectively, promoting cell scattering and metastasis by regulating a defined set of target genes. Indeed, the anti-tumoral AKT inhibitor API-2 promotes nuclear FOXO3a accumulation and metastasis of cells with high nuclear β-catenin content. Nuclear β-catenin confers resistance to the FOXO3a-mediated apoptosis induced by PI3K and AKT inhibitors in patient-derived primary cultures and in corresponding xenograft tumors in mice. This resistance is reversed by XAV-939, an inhibitor of Wnt–β-catenin signaling. In the presence of high nuclear β-catenin content, activation of FOXO3a by PI3K or AKT inhibitors makes it behave as a metastasis inductor rather than a proapoptotic tumor suppressor. We show that it is possible to evaluate the β-catenin status of patients' carcinomas and the response of patient-derived cells to target-directed drugs that accumulate FOXO3a in the nucleus before deciding on a course of treatment. We propose that this evaluation could be essential to the provision of a safer and more effective personalized treatment.
Similar articles
- Tankyrase Inhibition Blocks Wnt/β-Catenin Pathway and Reverts Resistance to PI3K and AKT Inhibitors in the Treatment of Colorectal Cancer.
Arqués O, Chicote I, Puig I, Tenbaum SP, Argilés G, Dienstmann R, Fernández N, Caratù G, Matito J, Silberschmidt D, Rodon J, Landolfi S, Prat A, Espín E, Charco R, Nuciforo P, Vivancos A, Shao W, Tabernero J, Palmer HG. Arqués O, et al. Clin Cancer Res. 2016 Feb 1;22(3):644-56. doi: 10.1158/1078-0432.CCR-14-3081. Epub 2015 Jul 29. Clin Cancer Res. 2016. PMID: 26224873 - Activation of FOXO3a is sufficient to reverse mitogen-activated protein/extracellular signal-regulated kinase kinase inhibitor chemoresistance in human cancer.
Yang JY, Chang CJ, Xia W, Wang Y, Wong KK, Engelman JA, Du Y, Andreeff M, Hortobagyi GN, Hung MC. Yang JY, et al. Cancer Res. 2010 Jun 1;70(11):4709-18. doi: 10.1158/0008-5472.CAN-09-4524. Epub 2010 May 18. Cancer Res. 2010. PMID: 20484037 Free PMC article. - FOXO3a and β-catenin co-localization: double trouble in colon cancer?
Yan Y, Lackner MR. Yan Y, et al. Nat Med. 2012 Jun 6;18(6):854-6. doi: 10.1038/nm.2799. Nat Med. 2012. PMID: 22673992 No abstract available. - Are Wnt/β-Catenin and PI3K/AKT/mTORC1 Distinct Pathways in Colorectal Cancer?
Prossomariti A, Piazzi G, Alquati C, Ricciardiello L. Prossomariti A, et al. Cell Mol Gastroenterol Hepatol. 2020;10(3):491-506. doi: 10.1016/j.jcmgh.2020.04.007. Epub 2020 Apr 22. Cell Mol Gastroenterol Hepatol. 2020. PMID: 32334125 Free PMC article. Review. - Natural bioactive compounds and FOXO3a in cancer therapeutics: An update.
Manoharan S, Prajapati K, Perumal E. Manoharan S, et al. Fitoterapia. 2024 Mar;173:105807. doi: 10.1016/j.fitote.2023.105807. Epub 2023 Dec 31. Fitoterapia. 2024. PMID: 38168566 Review.
Cited by
- Signaling cross-talk in the resistance to HER family receptor targeted therapy.
Yamaguchi H, Chang SS, Hsu JL, Hung MC. Yamaguchi H, et al. Oncogene. 2014 Feb 27;33(9):1073-81. doi: 10.1038/onc.2013.74. Epub 2013 Apr 1. Oncogene. 2014. PMID: 23542173 Free PMC article. Review. - Multiplicity of acquired cross-resistance in paclitaxel-resistant cancer cells is associated with feedback control of TUBB3 via FOXO3a-mediated ABCB1 regulation.
Aldonza MB, Hong JY, Alinsug MV, Song J, Lee SK. Aldonza MB, et al. Oncotarget. 2016 Jun 7;7(23):34395-419. doi: 10.18632/oncotarget.9118. Oncotarget. 2016. PMID: 27284014 Free PMC article. - Role of the beta catenin destruction complex in mediating chemotherapy-induced senescence-associated secretory phenotype.
Basu D, Reyes-Mugica M, Rebbaa A. Basu D, et al. PLoS One. 2012;7(12):e52188. doi: 10.1371/journal.pone.0052188. Epub 2012 Dec 18. PLoS One. 2012. PMID: 23272224 Free PMC article. - miR-22 targets YWHAZ to inhibit metastasis of hepatocellular carcinoma and its down-regulation predicts a poor survival.
Chen M, Hu W, Xiong CL, Qu Z, Yin CQ, Wang YH, Luo CL, Guan Q, Yuan CH, Wang FB. Chen M, et al. Oncotarget. 2016 Dec 6;7(49):80751-80764. doi: 10.18632/oncotarget.13037. Oncotarget. 2016. PMID: 27811373 Free PMC article. - Transcriptome-Based Traits of Radioresistant Sublines of Non-Small Cell Lung Cancer Cells.
Pustovalova M, Malakhov P, Guryanova A, Sorokin M, Suntsova M, Buzdin A, Osipov AN, Leonov S. Pustovalova M, et al. Int J Mol Sci. 2023 Feb 3;24(3):3042. doi: 10.3390/ijms24033042. Int J Mol Sci. 2023. PMID: 36769365 Free PMC article.
References
- Nat Rev Drug Discov. 2009 Aug;8(8):627-44 - PubMed
- PLoS One. 2009 Nov 24;4(11):e8013 - PubMed
- Cell. 2006 May 5;125(3):535-48 - PubMed
- Oncogene. 2008 Apr 7;27(16):2276-88 - PubMed
- Mol Cell Biol. 2009 Sep;29(18):4906-17 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous