RHOA inactivation enhances Wnt signalling and promotes colorectal cancer

被引:0
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作者
Paulo Rodrigues
Irati Macaya
Sarah Bazzocco
Rocco Mazzolini
Elena Andretta
Higinio Dopeso
Silvia Mateo-Lozano
Josipa Bilić
Fernando Cartón-García
Rocio Nieto
Lucia Suárez-López
Elsa Afonso
Stefania Landolfi
Javier Hernandez-Losa
Kazuto Kobayashi
Santiago Ramón y Cajal
Josep Tabernero
Niall C. Tebbutt
John M. Mariadason
Simo Schwartz
Diego Arango
机构
[1] Group of Molecular Oncology,Department of Pathology
[2] CIBBIM-Nanomedicine,Department of Molecular Genetics
[3] Vall d’Hebron University Hospital,Department of Medical Oncology
[4] Research Institute (VHIR),undefined
[5] Universitat Autònoma de Barcelona,undefined
[6] CIBER de Bioingeniería,undefined
[7] Biomateriales y Nanomedicina (CIBER-BBN),undefined
[8] Group of Drug Delivery and Targeting,undefined
[9] CIBBIM-Nanomedicine,undefined
[10] Vall d’Hebron University Hospital,undefined
[11] Research Institute (VHIR),undefined
[12] Universitat Autònoma de Barcelona,undefined
[13] Vall d’Hebron Hospital,undefined
[14] Institute of Biomedical Sciences,undefined
[15] Fukushima Medical University School of Medicine,undefined
[16] Vall d’Hebron University Hospital and Institute of Oncology (VHIO),undefined
[17] Universitat Autònoma de Barcelona,undefined
[18] Ludwig Institute for Cancer Research,undefined
[19] Melbourne-Branch,undefined
[20] Austin Health,undefined
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摘要
Activation of the small GTPase RHOA has strong oncogenic effects in many tumour types, although its role in colorectal cancer remains unclear. Here we show that RHOA inactivation contributes to colorectal cancer progression/metastasis, largely through the activation of Wnt/β-catenin signalling. RhoA inactivation in the murine intestine accelerates the tumorigenic process and in human colon cancer cells leads to the redistribution of β-catenin from the membrane to the nucleus and enhanced Wnt/β-catenin signalling, resulting in increased proliferation, invasion and de-differentiation. In mice, RHOA inactivation contributes to colon cancer metastasis and reduced RHOA levels were observed at metastatic sites compared with primary human colon tumours. Therefore, we have identified a new mechanism of activation of Wnt/β-catenin signalling and characterized the role of RHOA as a novel tumour suppressor in colorectal cancer. These results constitute a shift from the current paradigm and demonstrate that RHO GTPases can suppress tumour progression and metastasis.
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