Characterization of cytoplasmic cyclin D1 as a marker of invasiveness in cancer

Cyclin D1 (Ccnd1) is a proto-oncogen amplified in many different cancers and nuclear accumulation of Ccnd1 is a characteristic of tumor cells. Ccnd1 activates the transcription of a large set of genes involved in cell cycle progress and proliferation. However, Ccnd1 also targets cytoplasmic proteins...

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Detalles Bibliográficos
Autores: Pérez Fusté, Noel, Castelblanco Echavarría, Esmeralda, Felip Nogués, Isidre, Santacana Espasa, Maria, Fernández Hernández, Rita, Gatius Calderó, Sònia, Pedraza González, Neus, Pallares, Judit, Cemeli, Tània, Valls Marsal, Joan, Tarrés Escalona, Marc, Ferrezuelo, Francisco, Dolcet Roca, Xavier, Matias-Guiu, Xavier, Garí Marsol, Eloi
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2016
País:España
Institución:Universitat de Lleida (UdL)
Repositorio:Repositori Obert UdL
OAI Identifier:oai:repositori.udl.cat:10459.1/57224
Acceso en línea:https://doi.org/10.18632/oncotarget.8876
http://hdl.handle.net/10459.1/57224
Access Level:acceso abierto
Palabra clave:Cyclin D1
Tissue array
Cell invasion
Metastasis
Descripción
Sumario:Cyclin D1 (Ccnd1) is a proto-oncogen amplified in many different cancers and nuclear accumulation of Ccnd1 is a characteristic of tumor cells. Ccnd1 activates the transcription of a large set of genes involved in cell cycle progress and proliferation. However, Ccnd1 also targets cytoplasmic proteins involved in the regulation of cell migration and invasion. In this work, we have analyzed by immunohistochemistry the localization of Ccnd1 in endometrial, breast, prostate and colon carcinomas with different types of invasion. The number of cells displaying membranous or cytoplasmic Ccnd1 was significantly higher in peripheral cells than in inner cells in both collective and pushing invasion patterns of endometrial carcinoma, and in collective invasion pattern of colon carcinoma. Also, the cytoplasmic localization of Ccnd1 was higher when tumors infiltrated as single cells, budding or small clusters of cells. To evaluate cytoplasmic function of cyclin D1, we have built a variant (Ccnd1-CAAX) that remains attached to the cell membrane therefore sequestering this cyclin in the cytoplasm. Tumor cells harboring Ccnd1-CAAX showed high levels of invasiveness and metastatic potential compared to those containing the wild type allele of Ccnd1. However, Ccnd1- CAAX expression did not alter proliferative rates of tumor cells. We hypothesize that the role of Ccnd1 in the cytoplasm is mainly associated with the invasive capability of tumor cells. Moreover, we propose that subcellular localization of Ccnd1 is an interesting guideline to measure cancer outcome.