The atypical cyclin CNTD2 promotes colon cancer cell proliferation and migration

Colorectal cancer (CRC) is one of the most common cancers worldwide, with 8-10% of these tumours presenting a BRAF (V600E) mutation. Cyclins are known oncogenes deregulated in many cancers, but the role of the new subfamily of atypical cyclins remains elusive. Here we have performed a systematic ana...

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Detalles Bibliográficos
Autores: Sánchez Botet, Abril, Gasa, Laura, Quandt, Eva, Hernández Ortega, Sara, Jiménez Fàbrega, Xavier, Mezquita, Pau, Carrasco García, Miquel Àngel, Kron, Stephen J., Vidal-Bel, August, Villanueva Garatachea, Alberto, Ribeiro, Mariana P. C., Clotet Erra, Josep
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2018
País:España
Institución:Universidad de Barcelona
Repositorio:Dipòsit Digital de la UB
OAI Identifier:oai:diposit.ub.edu:2445/127976
Acceso en línea:https://hdl.handle.net/2445/127976
Access Level:acceso abierto
Palabra clave:Ciclines
Migració cel·lular
Càncer colorectal
Proliferació cel·lular
Cyclins
Cell migration
Colorectal cancer
Cell proliferation
Descripción
Sumario:Colorectal cancer (CRC) is one of the most common cancers worldwide, with 8-10% of these tumours presenting a BRAF (V600E) mutation. Cyclins are known oncogenes deregulated in many cancers, but the role of the new subfamily of atypical cyclins remains elusive. Here we have performed a systematic analysis of the protein expression levels of eight atypical cyclins in human CRC tumours and several cell lines, and found that CNTD2 is significantly upregulated in CRC tissue compared to the adjacent normal one. CNTD2 overexpression in CRC cell lines increases their proliferation capacity and migration, as well as spheroid formation capacity and anchorage-independent growth. Moreover, CNTD2 increases tumour growth in vivo on xenograft models of CRC with wild-type BRAF. Accordingly, CNTD2 downregulation significantly diminished the proliferation of wild-type BRAF CRC cells, suggesting that CNTD2 may represent a new prognostic factor and a promising drug target in the management of CRC.